Mutagenetix > Incidental Mutation

Incidental Mutation 'R2504:Hmcn1'

252061

Institutional Source

Beutler Lab

Gene Symbol

Hmcn1

Ensembl Gene

ENSMUSG00000066842

Gene Name

hemicentin 1

Synonyms

LOC240793, EG545370

MMRRC Submission

040412-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2504 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

150562524-150993435 bp(-) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 150686867 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Stop codon at position 2313 (C2313*)

Ref Sequence

ENSEMBL: ENSMUSP00000121500 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000074783] [ENSMUST00000137197]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000074783
AA Change: C2313*

SMART Domains

Protein: ENSMUSP00000074340
Gene: ENSMUSG00000066842
AA Change: C2313*

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
VWA	39	213	3e-1	SMART
IG_like	445	506	1.13e0	SMART
IGc2	532	598	2.32e-8	SMART
IGc2	624	688	1.24e-8	SMART
IGc2	714	779	7.52e-8	SMART
IGc2	805	874	2.19e-9	SMART
IGc2	902	967	5.15e-15	SMART
IGc2	993	1058	1.28e-10	SMART
IGc2	1092	1157	1.69e-10	SMART
IGc2	1183	1247	1.09e-13	SMART
IGc2	1278	1344	6.49e-12	SMART
IGc2	1372	1437	5.2e-11	SMART
IGc2	1465	1531	1.34e-13	SMART
IGc2	1559	1624	6.25e-14	SMART
IGc2	1653	1718	4.06e-13	SMART
IGc2	1746	1811	4.12e-14	SMART
IGc2	1838	1904	5.92e-15	SMART
IGc2	1932	1997	7.69e-14	SMART
IGc2	2023	2089	3.3e-13	SMART
IGc2	2115	2180	5e-13	SMART
IGc2	2208	2275	1.32e-12	SMART
IGc2	2304	2369	2.91e-14	SMART
IGc2	2398	2463	4e-12	SMART
IGc2	2491	2556	1.94e-19	SMART
IGc2	2587	2652	2.54e-14	SMART
IGc2	2686	2751	7.57e-13	SMART
IGc2	2789	2854	4.88e-16	SMART
IGc2	2884	2949	2.7e-9	SMART
IGc2	2976	3041	1.47e-10	SMART
IGc2	3071	3136	2.24e-15	SMART
IGc2	3163	3230	8.83e-14	SMART
IGc2	3258	3325	9.76e-16	SMART
IGc2	3354	3419	1.54e-13	SMART
IGc2	3447	3512	4.35e-13	SMART
IGc2	3540	3605	2e-12	SMART
IGc2	3633	3698	7.69e-14	SMART
IGc2	3724	3789	1.92e-14	SMART
IGc2	3815	3882	2.58e-6	SMART
IGc2	3908	3973	6.4e-11	SMART
IGc2	3999	4064	2.78e-11	SMART
IGc2	4090	4154	1.74e-12	SMART
low complexity region	4155	4160	N/A	INTRINSIC
IGc2	4180	4245	3.35e-14	SMART
IGc2	4271	4334	8.12e-13	SMART
IGc2	4361	4425	1.79e-14	SMART
IGc2	4451	4515	1.06e-11	SMART
TSP1	4531	4583	4.72e-15	SMART
TSP1	4588	4640	2.39e-16	SMART
TSP1	4645	4697	1.67e-15	SMART
TSP1	4702	4754	2.2e-15	SMART
TSP1	4759	4811	2.77e-12	SMART
TSP1	4816	4868	2.67e-14	SMART
Pfam:G2F	4869	5051	1.5e-57	PFAM
EGF_CA	5106	5145	4.38e-11	SMART
EGF_CA	5146	5190	4.49e-8	SMART
EGF_CA	5191	5228	2.38e-12	SMART
EGF_CA	5229	5270	6.8e-8	SMART
EGF_CA	5271	5313	3.51e-10	SMART
EGF_CA	5314	5354	4.32e-10	SMART
low complexity region	5384	5400	N/A	INTRINSIC
low complexity region	5401	5412	N/A	INTRINSIC
EGF_CA	5431	5470	2.78e-13	SMART
EGF	5474	5516	1.44e1	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000137197
AA Change: C2313*

SMART Domains

Protein: ENSMUSP00000121500
Gene: ENSMUSG00000066842
AA Change: C2313*

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
VWA	39	213	3e-1	SMART
IG_like	445	506	1.13e0	SMART
IGc2	532	598	2.32e-8	SMART
IGc2	624	688	1.24e-8	SMART
IGc2	714	779	7.52e-8	SMART
IGc2	805	874	2.19e-9	SMART
IGc2	902	967	5.15e-15	SMART
IGc2	993	1058	1.28e-10	SMART
IGc2	1092	1157	1.69e-10	SMART
IGc2	1183	1247	1.09e-13	SMART
IGc2	1278	1344	6.49e-12	SMART
IGc2	1372	1437	5.2e-11	SMART
IGc2	1465	1531	1.34e-13	SMART
IGc2	1559	1624	6.25e-14	SMART
IGc2	1653	1718	4.06e-13	SMART
IGc2	1746	1811	4.12e-14	SMART
IGc2	1838	1904	5.92e-15	SMART
IGc2	1932	1997	7.69e-14	SMART
IGc2	2023	2089	3.3e-13	SMART
IGc2	2115	2180	5e-13	SMART
IGc2	2208	2275	1.32e-12	SMART
IGc2	2304	2369	2.91e-14	SMART
IGc2	2398	2463	4e-12	SMART
IGc2	2491	2556	1.94e-19	SMART
IGc2	2587	2652	2.54e-14	SMART
IGc2	2686	2751	7.57e-13	SMART
IGc2	2789	2854	4.88e-16	SMART
IGc2	2884	2949	2.7e-9	SMART
IGc2	2976	3041	1.47e-10	SMART
IGc2	3071	3136	2.24e-15	SMART
IGc2	3163	3230	8.83e-14	SMART
IGc2	3258	3325	9.76e-16	SMART
IGc2	3354	3419	1.54e-13	SMART
IGc2	3447	3512	4.35e-13	SMART
IGc2	3540	3605	2e-12	SMART
IGc2	3633	3698	7.69e-14	SMART
IGc2	3724	3789	1.92e-14	SMART
IGc2	3815	3882	2.58e-6	SMART
IGc2	3908	3973	6.4e-11	SMART
IGc2	3999	4064	2.78e-11	SMART
IGc2	4090	4154	1.74e-12	SMART
low complexity region	4155	4160	N/A	INTRINSIC
IGc2	4180	4245	3.35e-14	SMART
IGc2	4271	4334	8.12e-13	SMART
IGc2	4361	4425	1.79e-14	SMART
IGc2	4451	4515	1.06e-11	SMART
TSP1	4531	4583	4.72e-15	SMART
TSP1	4588	4640	2.39e-16	SMART
TSP1	4645	4697	1.67e-15	SMART
TSP1	4702	4754	2.2e-15	SMART
TSP1	4759	4811	2.77e-12	SMART
TSP1	4816	4868	2.67e-14	SMART
PDB:1GL4\|A	4869	5082	3e-6	PDB
SCOP:d1gl4a1	4869	5082	3e-79	SMART
EGF_CA	5106	5145	4.38e-11	SMART
EGF_CA	5146	5190	4.49e-8	SMART
EGF_CA	5191	5228	2.38e-12	SMART
EGF_CA	5229	5270	6.8e-8	SMART
EGF_CA	5271	5313	3.51e-10	SMART
EGF_CA	5314	5353	2.78e-13	SMART
EGF	5357	5399	1.44e1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000177268

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.4%
20x: 95.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a large extracellular member of the immunoglobulin superfamily. A similar protein in C. elegans forms long, fine tracks at specific extracellular sites that are involved in many processes such as stabilization of the germline syncytium, anchorage of mechanosensory neurons to the epidermis, and organization of hemidesmosomes in the epidermis. Mutations in this gene may be associated with age-related macular degeneration. [provided by RefSeq, Jul 2008]

Allele List at MGI

All alleles(4) : Targeted(3) Gene trapped(1)

Other mutations in this stock

Total: 113 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aatk	T	C	11: 120,018,855 (GRCm38)	D28G	probably benign	Het
Abcg1	T	A	17: 31,092,395 (GRCm38)	S125T	probably damaging	Het
Actbl2	T	C	13: 111,256,183 (GRCm38)	S351P	possibly damaging	Het
Ankrd34b	A	G	13: 92,439,061 (GRCm38)		probably null	Het
BC051665	C	T	13: 60,782,654 (GRCm38)	V295I	probably benign	Het
C1qtnf2	A	G	11: 43,491,156 (GRCm38)	N265S	probably damaging	Het
Ccdc14	C	T	16: 34,721,850 (GRCm38)	R573*	probably null	Het
Cd55b	A	T	1: 130,409,875 (GRCm38)	Y247N	probably damaging	Het
Celsr2	A	T	3: 108,413,591 (GRCm38)	V635E	probably benign	Het
Clec16a	T	C	16: 10,559,687 (GRCm38)		probably benign	Het
Clec4b1	A	G	6: 123,065,945 (GRCm38)	Y41C	probably damaging	Het
Cntn5	A	T	9: 10,172,121 (GRCm38)	D19E	probably benign	Het
Cop1	A	G	1: 159,232,805 (GRCm38)	N53S	probably damaging	Het
Cplane1	G	A	15: 8,219,216 (GRCm38)	E1750K	probably damaging	Het
Csad	A	T	15: 102,188,667 (GRCm38)	M1K	probably null	Het
Cyb5rl	A	G	4: 107,080,945 (GRCm38)	I200V	probably benign	Het
Cyp26a1	A	G	19: 37,698,342 (GRCm38)	T81A	probably damaging	Het
Cyp2d12	A	T	15: 82,559,036 (GRCm38)	H433L	probably benign	Het
D7Ertd443e	T	A	7: 134,349,479 (GRCm38)		probably null	Het
Dennd1b	A	G	1: 139,170,170 (GRCm38)		probably benign	Het
Dmap1	G	T	4: 117,675,298 (GRCm38)	T357K	probably damaging	Het
Dzip1	G	T	14: 118,881,044 (GRCm38)	T759K	probably benign	Het
Elmo2	A	G	2: 165,298,687 (GRCm38)	V300A	probably damaging	Het
Eml5	T	C	12: 98,844,105 (GRCm38)	D864G	possibly damaging	Het
Ep400	A	G	5: 110,668,645 (GRCm38)	V2670A	probably damaging	Het
Epha3	T	A	16: 63,603,625 (GRCm38)	I534F	probably damaging	Het
Epha4	A	C	1: 77,382,991 (GRCm38)	Y742D	probably damaging	Het
Ergic2	A	G	6: 148,204,774 (GRCm38)		probably null	Het
Ero1a	A	T	14: 45,299,088 (GRCm38)		probably null	Het
Fam229a	A	G	4: 129,491,486 (GRCm38)	D70G	probably damaging	Het
Fbn2	C	T	18: 58,093,359 (GRCm38)	R781Q	probably damaging	Het
Fbxo16	A	T	14: 65,270,714 (GRCm38)		probably benign	Het
Fbxo39	T	A	11: 72,317,285 (GRCm38)	S154R	probably benign	Het
Fer	T	A	17: 63,991,580 (GRCm38)		probably null	Het
Filip1l	A	T	16: 57,571,047 (GRCm38)	D428V	probably damaging	Het
Filip1l	A	G	16: 57,570,662 (GRCm38)	I538V	possibly damaging	Het
Fsip2	T	C	2: 82,979,610 (GRCm38)	I2091T	possibly damaging	Het
Glyat	A	C	19: 12,651,398 (GRCm38)	T186P	possibly damaging	Het
Gm10604	A	G	4: 11,980,083 (GRCm38)	S74P	unknown	Het
Gm4787	T	G	12: 81,379,137 (GRCm38)	K82N	possibly damaging	Het
Hectd4	T	C	5: 121,220,620 (GRCm38)	I50T	unknown	Het
Hectd4	T	C	5: 121,263,967 (GRCm38)	S373P	possibly damaging	Het
Hrob	T	C	11: 102,255,296 (GRCm38)	Y133H	possibly damaging	Het
Igfn1	A	T	1: 135,969,316 (GRCm38)	S1171T	probably benign	Het
Ints8	T	C	4: 11,241,642 (GRCm38)	D267G	probably benign	Het
Itln1	A	G	1: 171,529,159 (GRCm38)	C251R	probably damaging	Het
Jcad	C	T	18: 4,674,026 (GRCm38)	T596M	probably damaging	Het
Kcnj16	C	T	11: 111,025,583 (GRCm38)	T357M	probably benign	Het
Kif13a	G	A	13: 46,814,200 (GRCm38)	T346M	probably damaging	Het
Klhl24	G	A	16: 20,120,167 (GRCm38)	A491T	probably benign	Het
Kntc1	C	T	5: 123,778,347 (GRCm38)	Q748*	probably null	Het
Krt25	T	A	11: 99,317,296 (GRCm38)	K369*	probably null	Het
Krt75	C	T	15: 101,568,031 (GRCm38)	R433Q	probably benign	Het
Krt76	A	G	15: 101,884,858 (GRCm38)	F582L	unknown	Het
Lysmd1	G	A	3: 95,138,397 (GRCm38)	V182I	probably benign	Het
Mab21l2	T	A	3: 86,547,555 (GRCm38)	E46V	probably damaging	Het
Magi2	A	T	5: 20,358,936 (GRCm38)	K355N	probably damaging	Het
Marchf10	T	C	11: 105,385,572 (GRCm38)	D630G	probably damaging	Het
Mast4	A	T	13: 102,738,639 (GRCm38)	I1215N	probably damaging	Het
Nckap1	G	A	2: 80,530,218 (GRCm38)	T523I	probably benign	Het
Nexmif	T	A	X: 104,084,393 (GRCm38)	D1306V	probably damaging	Het
Nfkb1	A	C	3: 135,589,329 (GRCm38)	I918R	possibly damaging	Het
Nt5el	A	G	13: 105,109,742 (GRCm38)	I270M	probably benign	Het
Nup50	A	T	15: 84,933,658 (GRCm38)	T93S	probably benign	Het
Nwd2	T	C	5: 63,804,374 (GRCm38)	Y434H	probably benign	Het
Or13a28	T	C	7: 140,638,484 (GRCm38)	V261A	probably benign	Het
Osbpl1a	C	A	18: 12,905,031 (GRCm38)	V288L	probably benign	Het
Pan3	A	G	5: 147,527,036 (GRCm38)	E562G	possibly damaging	Het
Pappa	T	A	4: 65,180,889 (GRCm38)	Y548*	probably null	Het
Phf3	A	T	1: 30,810,789 (GRCm38)	L1181Q	probably damaging	Het
Phip	T	C	9: 82,915,339 (GRCm38)	H537R	possibly damaging	Het
Pkhd1l1	T	C	15: 44,485,428 (GRCm38)	I240T	probably damaging	Het
Pole	G	A	5: 110,290,502 (GRCm38)		probably null	Het
Polq	T	A	16: 37,011,942 (GRCm38)	S15T	unknown	Het
Prrt2	T	C	7: 127,020,224 (GRCm38)	E23G	possibly damaging	Het
Prss37	A	T	6: 40,517,826 (GRCm38)		probably null	Het
Prune2	T	C	19: 17,000,036 (GRCm38)	L45P	probably damaging	Het
Psd	A	T	19: 46,324,913 (GRCm38)	M6K	possibly damaging	Het
Psmd1	A	G	1: 86,089,997 (GRCm38)	E510G	possibly damaging	Het
Ptch1	T	G	13: 63,524,959 (GRCm38)	E944A	probably benign	Het
Pxdn	T	A	12: 30,003,406 (GRCm38)	I1194N	probably damaging	Het
Rbp3	C	T	14: 33,956,018 (GRCm38)	T641M	probably damaging	Het
Rgmb	C	A	17: 15,807,647 (GRCm38)	R270L	probably benign	Het
Rpgrip1l	A	G	8: 91,280,716 (GRCm38)		probably null	Het
Rps2	G	A	17: 24,720,379 (GRCm38)		probably benign	Het
Rsbn1l	G	T	5: 20,902,366 (GRCm38)	A550E	probably damaging	Het
S1pr4	C	T	10: 81,499,304 (GRCm38)	R112H	probably benign	Het
Scfd2	T	C	5: 74,531,177 (GRCm38)	N148S	probably damaging	Het
Scin	C	T	12: 40,081,706 (GRCm38)	M276I	probably benign	Het
Sec24d	T	C	3: 123,353,606 (GRCm38)	I708T	possibly damaging	Het
Skint11	T	A	4: 114,228,812 (GRCm38)	F41I	possibly damaging	Het
Slc15a4	A	T	5: 127,617,239 (GRCm38)	F44Y	possibly damaging	Het
Slc6a18	A	G	13: 73,675,806 (GRCm38)	Y72H	probably benign	Het
Slc7a11	A	T	3: 50,377,746 (GRCm38)		probably null	Het
Slc7a14	G	T	3: 31,237,501 (GRCm38)	N209K	possibly damaging	Het
Sstr2	T	C	11: 113,624,431 (GRCm38)	C59R	probably damaging	Het
Stab1	A	G	14: 31,163,040 (GRCm38)		probably null	Het
Stag1	G	T	9: 100,866,210 (GRCm38)	S475I	probably damaging	Het
Stxbp5l	A	G	16: 37,115,667 (GRCm38)	Y1183H	probably damaging	Het
Svep1	A	T	4: 58,135,628 (GRCm38)		probably null	Het
Tm9sf2	A	G	14: 122,158,684 (GRCm38)	T653A	probably benign	Het
Tmeff1	T	C	4: 48,662,059 (GRCm38)	S366P	possibly damaging	Het
Tnnt2	G	T	1: 135,852,065 (GRCm38)	W300L	probably damaging	Het
Traj32	A	G	14: 54,186,103 (GRCm38)		probably benign	Het
Trp53bp2	A	T	1: 182,441,639 (GRCm38)	M223L	probably benign	Het
Tsga10	G	A	1: 37,815,677 (GRCm38)	T246M	probably damaging	Het
Txn2	A	T	15: 77,926,670 (GRCm38)		probably benign	Het
Ubr3	T	A	2: 69,938,198 (GRCm38)	F450I	probably damaging	Het
Usp47	T	C	7: 112,104,470 (GRCm38)		probably null	Het
Vars2	C	T	17: 35,664,793 (GRCm38)	R244Q	probably damaging	Het
Xrra1	T	A	7: 99,897,596 (GRCm38)	F251L	probably damaging	Het
Zfp804a	G	A	2: 82,257,519 (GRCm38)	R564Q	probably benign	Het
Zfp983	T	C	17: 21,658,967 (GRCm38)	C29R	probably damaging	Het

Other mutations in Hmcn1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00417:Hmcn1	APN	1	150,677,278 (GRCm38)	missense	probably benign
IGL00571:Hmcn1	APN	1	150,638,999 (GRCm38)	missense	probably benign	0.05
IGL00726:Hmcn1	APN	1	150,806,366 (GRCm38)	critical splice donor site	probably null
IGL00802:Hmcn1	APN	1	150,664,936 (GRCm38)	missense	probably benign	0.19
IGL00824:Hmcn1	APN	1	150,656,734 (GRCm38)	missense	probably damaging	1.00
IGL00834:Hmcn1	APN	1	150,630,340 (GRCm38)	missense	probably benign	0.00
IGL00843:Hmcn1	APN	1	150,610,713 (GRCm38)	missense	possibly damaging	0.95
IGL00845:Hmcn1	APN	1	150,605,006 (GRCm38)	missense	probably damaging	0.98
IGL00851:Hmcn1	APN	1	150,582,301 (GRCm38)	missense	probably benign	0.02
IGL00909:Hmcn1	APN	1	150,638,869 (GRCm38)	missense	probably benign	0.12
IGL01074:Hmcn1	APN	1	150,627,033 (GRCm38)	missense	possibly damaging	0.82
IGL01112:Hmcn1	APN	1	150,632,552 (GRCm38)	splice site	probably benign
IGL01304:Hmcn1	APN	1	150,622,924 (GRCm38)	missense	probably damaging	0.99
IGL01307:Hmcn1	APN	1	150,745,001 (GRCm38)	missense	possibly damaging	0.84
IGL01318:Hmcn1	APN	1	150,719,240 (GRCm38)	missense	probably damaging	1.00
IGL01403:Hmcn1	APN	1	150,593,097 (GRCm38)	missense	probably damaging	1.00
IGL01417:Hmcn1	APN	1	150,859,239 (GRCm38)	missense	probably damaging	1.00
IGL01503:Hmcn1	APN	1	150,605,072 (GRCm38)	missense	probably benign	0.38
IGL01509:Hmcn1	APN	1	150,609,631 (GRCm38)	missense	probably damaging	1.00
IGL01550:Hmcn1	APN	1	150,598,397 (GRCm38)	missense	probably damaging	1.00
IGL01601:Hmcn1	APN	1	150,627,413 (GRCm38)	missense	probably benign	0.01
IGL01617:Hmcn1	APN	1	150,672,032 (GRCm38)	missense	probably benign	0.05
IGL01636:Hmcn1	APN	1	150,580,233 (GRCm38)	missense	probably damaging	1.00
IGL01662:Hmcn1	APN	1	150,737,299 (GRCm38)	missense	possibly damaging	0.46
IGL01693:Hmcn1	APN	1	150,583,280 (GRCm38)	missense	probably damaging	1.00
IGL01723:Hmcn1	APN	1	150,744,960 (GRCm38)	missense	probably benign	0.01
IGL01776:Hmcn1	APN	1	150,672,038 (GRCm38)	missense	possibly damaging	0.70
IGL01783:Hmcn1	APN	1	150,615,300 (GRCm38)	missense	possibly damaging	0.60
IGL01789:Hmcn1	APN	1	150,690,601 (GRCm38)	missense	probably damaging	1.00
IGL01900:Hmcn1	APN	1	150,742,260 (GRCm38)	splice site	probably benign
IGL01906:Hmcn1	APN	1	150,667,887 (GRCm38)	missense	probably benign	0.01
IGL01947:Hmcn1	APN	1	150,732,892 (GRCm38)	missense	possibly damaging	0.93
IGL01958:Hmcn1	APN	1	150,603,871 (GRCm38)	missense	probably benign	0.01
IGL02002:Hmcn1	APN	1	150,615,298 (GRCm38)	missense	probably damaging	1.00
IGL02058:Hmcn1	APN	1	150,704,181 (GRCm38)	missense	probably benign	0.02
IGL02115:Hmcn1	APN	1	150,630,728 (GRCm38)	missense	probably damaging	1.00
IGL02127:Hmcn1	APN	1	150,722,607 (GRCm38)	missense	probably benign
IGL02155:Hmcn1	APN	1	150,563,598 (GRCm38)	missense	probably damaging	1.00
IGL02222:Hmcn1	APN	1	150,806,401 (GRCm38)	missense	probably benign	0.05
IGL02293:Hmcn1	APN	1	150,664,915 (GRCm38)	missense	probably damaging	0.97
IGL02398:Hmcn1	APN	1	150,802,897 (GRCm38)	missense	possibly damaging	0.78
IGL02420:Hmcn1	APN	1	150,722,424 (GRCm38)	missense	probably damaging	1.00
IGL02553:Hmcn1	APN	1	150,993,023 (GRCm38)	missense	probably benign	0.12
IGL02561:Hmcn1	APN	1	150,809,726 (GRCm38)	missense	probably benign	0.32
IGL02569:Hmcn1	APN	1	150,697,493 (GRCm38)	missense	probably benign	0.01
IGL02607:Hmcn1	APN	1	150,744,995 (GRCm38)	missense	possibly damaging	0.88
IGL02676:Hmcn1	APN	1	150,619,009 (GRCm38)	missense	probably benign	0.01
IGL02725:Hmcn1	APN	1	150,604,903 (GRCm38)	missense	possibly damaging	0.92
IGL02726:Hmcn1	APN	1	150,656,694 (GRCm38)	nonsense	probably null
IGL02735:Hmcn1	APN	1	150,646,832 (GRCm38)	missense	probably benign	0.02
IGL02737:Hmcn1	APN	1	150,563,828 (GRCm38)	missense	probably damaging	1.00
IGL02892:Hmcn1	APN	1	150,675,974 (GRCm38)	critical splice donor site	probably null
IGL02927:Hmcn1	APN	1	150,577,278 (GRCm38)	missense	probably damaging	1.00
IGL02931:Hmcn1	APN	1	150,657,207 (GRCm38)	missense	probably benign	0.37
IGL02936:Hmcn1	APN	1	150,697,522 (GRCm38)	missense	probably damaging	0.98
IGL02985:Hmcn1	APN	1	150,671,917 (GRCm38)	missense	probably damaging	1.00
IGL03027:Hmcn1	APN	1	150,808,539 (GRCm38)	missense	probably benign
IGL03195:Hmcn1	APN	1	150,802,909 (GRCm38)	missense	probably benign	0.06
IGL03217:Hmcn1	APN	1	150,743,667 (GRCm38)	missense	possibly damaging	0.58
IGL03232:Hmcn1	APN	1	150,770,352 (GRCm38)	splice site	probably benign
IGL03268:Hmcn1	APN	1	150,772,510 (GRCm38)	missense	probably damaging	1.00
IGL03271:Hmcn1	APN	1	150,598,424 (GRCm38)	missense	possibly damaging	0.92
IGL03304:Hmcn1	APN	1	150,630,231 (GRCm38)	missense	probably damaging	0.97
IGL03329:Hmcn1	APN	1	150,732,910 (GRCm38)	missense	probably damaging	1.00
IGL03339:Hmcn1	APN	1	150,701,969 (GRCm38)	missense	probably benign	0.04
IGL03368:Hmcn1	APN	1	150,663,872 (GRCm38)	missense	probably damaging	1.00
Backbone	UTSW	1	150,622,994 (GRCm38)	missense	probably benign	0.09
Cambrian	UTSW	1	150,732,846 (GRCm38)	missense	probably damaging	1.00
chordate	UTSW	1	150,587,015 (GRCm38)	missense	probably benign	0.00
Justamere	UTSW	1	150,588,257 (GRCm38)	missense	probably damaging	1.00
Lancelet	UTSW	1	150,675,540 (GRCm38)	missense	probably benign	0.00
notochord	UTSW	1	150,770,293 (GRCm38)	missense	probably benign	0.00
wippoorwill	UTSW	1	150,732,946 (GRCm38)	missense	probably damaging	1.00
BB004:Hmcn1	UTSW	1	150,609,775 (GRCm38)	missense	probably damaging	1.00
BB014:Hmcn1	UTSW	1	150,609,775 (GRCm38)	missense	probably damaging	1.00
IGL02991:Hmcn1	UTSW	1	150,738,658 (GRCm38)	missense	possibly damaging	0.56
P0017:Hmcn1	UTSW	1	150,720,689 (GRCm38)	missense	possibly damaging	0.49
PIT1430001:Hmcn1	UTSW	1	150,808,737 (GRCm38)	missense	probably benign	0.00
PIT4514001:Hmcn1	UTSW	1	150,669,487 (GRCm38)	missense	possibly damaging	0.93
R0006:Hmcn1	UTSW	1	150,808,676 (GRCm38)	missense	probably damaging	0.99
R0018:Hmcn1	UTSW	1	150,652,551 (GRCm38)	missense	probably benign	0.16
R0052:Hmcn1	UTSW	1	150,677,406 (GRCm38)	missense	probably damaging	1.00
R0107:Hmcn1	UTSW	1	150,587,015 (GRCm38)	missense	probably benign	0.00
R0115:Hmcn1	UTSW	1	150,808,647 (GRCm38)	missense	possibly damaging	0.88
R0149:Hmcn1	UTSW	1	150,677,324 (GRCm38)	missense	probably benign	0.00
R0152:Hmcn1	UTSW	1	150,663,879 (GRCm38)	missense	probably benign	0.01
R0381:Hmcn1	UTSW	1	150,603,811 (GRCm38)	missense	probably damaging	1.00
R0398:Hmcn1	UTSW	1	150,798,814 (GRCm38)	missense	possibly damaging	0.83
R0414:Hmcn1	UTSW	1	150,715,822 (GRCm38)	missense	possibly damaging	0.72
R0494:Hmcn1	UTSW	1	150,732,792 (GRCm38)	splice site	probably benign
R0503:Hmcn1	UTSW	1	150,859,252 (GRCm38)	missense	probably damaging	1.00
R0504:Hmcn1	UTSW	1	150,876,419 (GRCm38)	splice site	probably benign
R0506:Hmcn1	UTSW	1	150,742,341 (GRCm38)	missense	possibly damaging	0.69
R0554:Hmcn1	UTSW	1	150,719,117 (GRCm38)	missense	probably benign	0.34
R0576:Hmcn1	UTSW	1	150,650,017 (GRCm38)	nonsense	probably null
R0599:Hmcn1	UTSW	1	150,609,801 (GRCm38)	missense	possibly damaging	0.91
R0605:Hmcn1	UTSW	1	150,657,376 (GRCm38)	critical splice donor site	probably null
R0607:Hmcn1	UTSW	1	150,638,900 (GRCm38)	missense	probably benign	0.01
R0620:Hmcn1	UTSW	1	150,594,016 (GRCm38)	missense	probably benign	0.04
R0626:Hmcn1	UTSW	1	150,798,719 (GRCm38)	splice site	probably null
R0699:Hmcn1	UTSW	1	150,819,410 (GRCm38)	missense	probably damaging	1.00
R0765:Hmcn1	UTSW	1	150,808,787 (GRCm38)	missense	probably damaging	1.00
R0782:Hmcn1	UTSW	1	150,753,665 (GRCm38)	missense	possibly damaging	0.82
R0783:Hmcn1	UTSW	1	150,650,073 (GRCm38)	missense	probably damaging	1.00
R0841:Hmcn1	UTSW	1	150,679,607 (GRCm38)	splice site	probably null
R0975:Hmcn1	UTSW	1	150,577,377 (GRCm38)	missense	probably benign	0.00
R1070:Hmcn1	UTSW	1	150,689,590 (GRCm38)	missense	probably damaging	0.98
R1118:Hmcn1	UTSW	1	150,618,928 (GRCm38)	missense	possibly damaging	0.56
R1119:Hmcn1	UTSW	1	150,618,928 (GRCm38)	missense	possibly damaging	0.56
R1145:Hmcn1	UTSW	1	150,679,607 (GRCm38)	splice site	probably null
R1145:Hmcn1	UTSW	1	150,679,607 (GRCm38)	splice site	probably null
R1233:Hmcn1	UTSW	1	150,749,026 (GRCm38)	missense	probably benign
R1234:Hmcn1	UTSW	1	150,753,654 (GRCm38)	nonsense	probably null
R1291:Hmcn1	UTSW	1	150,748,191 (GRCm38)	missense	probably damaging	1.00
R1334:Hmcn1	UTSW	1	150,586,468 (GRCm38)	missense	possibly damaging	0.73
R1372:Hmcn1	UTSW	1	150,680,715 (GRCm38)	missense	probably benign	0.22
R1424:Hmcn1	UTSW	1	150,646,794 (GRCm38)	missense	probably benign	0.00
R1450:Hmcn1	UTSW	1	150,652,506 (GRCm38)	splice site	probably benign
R1458:Hmcn1	UTSW	1	150,609,700 (GRCm38)	missense	probably damaging	1.00
R1467:Hmcn1	UTSW	1	150,689,590 (GRCm38)	missense	probably damaging	0.98
R1467:Hmcn1	UTSW	1	150,689,590 (GRCm38)	missense	probably damaging	0.98
R1473:Hmcn1	UTSW	1	150,772,552 (GRCm38)	missense	probably benign	0.03
R1517:Hmcn1	UTSW	1	150,669,421 (GRCm38)	missense	probably damaging	1.00
R1527:Hmcn1	UTSW	1	150,773,803 (GRCm38)	missense	probably benign	0.00
R1557:Hmcn1	UTSW	1	150,734,532 (GRCm38)	missense	possibly damaging	0.86
R1576:Hmcn1	UTSW	1	150,657,241 (GRCm38)	missense	possibly damaging	0.77
R1617:Hmcn1	UTSW	1	150,745,027 (GRCm38)	missense	probably damaging	0.98
R1635:Hmcn1	UTSW	1	150,669,558 (GRCm38)	missense	probably benign	0.00
R1655:Hmcn1	UTSW	1	150,630,333 (GRCm38)	missense	probably benign	0.03
R1698:Hmcn1	UTSW	1	150,565,369 (GRCm38)	nonsense	probably null
R1710:Hmcn1	UTSW	1	150,675,984 (GRCm38)	missense	probably damaging	1.00
R1717:Hmcn1	UTSW	1	150,859,186 (GRCm38)	missense	probably damaging	1.00
R1753:Hmcn1	UTSW	1	150,586,468 (GRCm38)	missense	possibly damaging	0.73
R1756:Hmcn1	UTSW	1	150,599,030 (GRCm38)	missense	probably damaging	1.00
R1772:Hmcn1	UTSW	1	150,563,568 (GRCm38)	missense	probably damaging	0.99
R1793:Hmcn1	UTSW	1	150,749,083 (GRCm38)	missense	probably benign	0.01
R1794:Hmcn1	UTSW	1	150,627,152 (GRCm38)	missense	probably damaging	0.98
R1794:Hmcn1	UTSW	1	150,598,285 (GRCm38)	missense	probably benign	0.00
R1856:Hmcn1	UTSW	1	150,721,664 (GRCm38)	missense	probably benign	0.02
R1859:Hmcn1	UTSW	1	150,657,193 (GRCm38)	missense	probably damaging	1.00
R1862:Hmcn1	UTSW	1	150,638,900 (GRCm38)	missense	probably benign	0.01
R1865:Hmcn1	UTSW	1	150,603,812 (GRCm38)	missense	probably damaging	1.00
R1874:Hmcn1	UTSW	1	150,720,695 (GRCm38)	missense	probably damaging	1.00
R1880:Hmcn1	UTSW	1	150,638,900 (GRCm38)	missense	probably benign	0.01
R1881:Hmcn1	UTSW	1	150,638,900 (GRCm38)	missense	probably benign	0.01
R1886:Hmcn1	UTSW	1	150,577,295 (GRCm38)	missense	probably benign	0.02
R1888:Hmcn1	UTSW	1	150,819,500 (GRCm38)	missense	possibly damaging	0.82
R1888:Hmcn1	UTSW	1	150,819,500 (GRCm38)	missense	possibly damaging	0.82
R1899:Hmcn1	UTSW	1	150,657,451 (GRCm38)	missense	probably damaging	1.00
R1905:Hmcn1	UTSW	1	150,992,855 (GRCm38)	missense	probably damaging	1.00
R1912:Hmcn1	UTSW	1	150,604,882 (GRCm38)	missense	probably benign	0.28
R1959:Hmcn1	UTSW	1	150,649,676 (GRCm38)	missense	probably benign	0.00
R1960:Hmcn1	UTSW	1	150,677,376 (GRCm38)	missense	possibly damaging	0.72
R1960:Hmcn1	UTSW	1	150,675,991 (GRCm38)	missense	probably benign	0.00
R2001:Hmcn1	UTSW	1	150,738,613 (GRCm38)	missense	possibly damaging	0.81
R2011:Hmcn1	UTSW	1	150,677,334 (GRCm38)	missense	probably benign	0.01
R2075:Hmcn1	UTSW	1	150,577,323 (GRCm38)	missense	possibly damaging	0.86
R2136:Hmcn1	UTSW	1	150,633,659 (GRCm38)	missense	probably damaging	1.00
R2192:Hmcn1	UTSW	1	150,715,815 (GRCm38)	missense	probably damaging	0.97
R2267:Hmcn1	UTSW	1	150,599,010 (GRCm38)	missense	probably benign	0.00
R2268:Hmcn1	UTSW	1	150,624,598 (GRCm38)	splice site	probably benign
R2303:Hmcn1	UTSW	1	150,704,226 (GRCm38)	missense	probably damaging	1.00
R2330:Hmcn1	UTSW	1	150,652,678 (GRCm38)	splice site	probably benign
R2338:Hmcn1	UTSW	1	150,622,934 (GRCm38)	missense	possibly damaging	0.89
R2380:Hmcn1	UTSW	1	150,565,384 (GRCm38)	missense	probably benign	0.01
R2405:Hmcn1	UTSW	1	150,860,341 (GRCm38)	missense	probably damaging	1.00
R2443:Hmcn1	UTSW	1	150,599,032 (GRCm38)	missense	probably benign	0.01
R2496:Hmcn1	UTSW	1	150,615,221 (GRCm38)	missense	probably benign	0.01
R2519:Hmcn1	UTSW	1	150,773,820 (GRCm38)	nonsense	probably null
R2520:Hmcn1	UTSW	1	150,743,647 (GRCm38)	missense	possibly damaging	0.72
R2679:Hmcn1	UTSW	1	150,652,575 (GRCm38)	missense	possibly damaging	0.67
R2831:Hmcn1	UTSW	1	150,630,652 (GRCm38)	critical splice donor site	probably null
R2847:Hmcn1	UTSW	1	150,563,599 (GRCm38)	nonsense	probably null
R2849:Hmcn1	UTSW	1	150,563,599 (GRCm38)	nonsense	probably null
R2869:Hmcn1	UTSW	1	150,738,716 (GRCm38)	missense	possibly damaging	0.95
R2869:Hmcn1	UTSW	1	150,738,716 (GRCm38)	missense	possibly damaging	0.95
R2871:Hmcn1	UTSW	1	150,738,716 (GRCm38)	missense	possibly damaging	0.95
R2871:Hmcn1	UTSW	1	150,738,716 (GRCm38)	missense	possibly damaging	0.95
R2872:Hmcn1	UTSW	1	150,738,716 (GRCm38)	missense	possibly damaging	0.95
R2872:Hmcn1	UTSW	1	150,738,716 (GRCm38)	missense	possibly damaging	0.95
R2873:Hmcn1	UTSW	1	150,738,716 (GRCm38)	missense	possibly damaging	0.95
R2897:Hmcn1	UTSW	1	150,802,873 (GRCm38)	missense	probably damaging	1.00
R2905:Hmcn1	UTSW	1	150,749,035 (GRCm38)	missense	probably damaging	1.00
R3498:Hmcn1	UTSW	1	150,605,102 (GRCm38)	missense	probably damaging	0.98
R3499:Hmcn1	UTSW	1	150,605,102 (GRCm38)	missense	probably damaging	0.98
R3724:Hmcn1	UTSW	1	150,689,518 (GRCm38)	missense	possibly damaging	0.82
R3765:Hmcn1	UTSW	1	150,745,025 (GRCm38)	missense	possibly damaging	0.72
R3778:Hmcn1	UTSW	1	150,802,824 (GRCm38)	missense	possibly damaging	0.95
R3790:Hmcn1	UTSW	1	150,622,994 (GRCm38)	missense	probably benign	0.09
R3796:Hmcn1	UTSW	1	150,586,418 (GRCm38)	missense	probably damaging	1.00
R3811:Hmcn1	UTSW	1	150,649,577 (GRCm38)	critical splice donor site	probably null
R3825:Hmcn1	UTSW	1	150,586,965 (GRCm38)	missense	probably benign	0.28
R3890:Hmcn1	UTSW	1	150,635,195 (GRCm38)	missense	probably damaging	1.00
R3891:Hmcn1	UTSW	1	150,635,195 (GRCm38)	missense	probably damaging	1.00
R3892:Hmcn1	UTSW	1	150,635,195 (GRCm38)	missense	probably damaging	1.00
R3918:Hmcn1	UTSW	1	150,690,610 (GRCm38)	missense	probably benign	0.00
R3964:Hmcn1	UTSW	1	150,573,569 (GRCm38)	missense	probably benign	0.00
R4005:Hmcn1	UTSW	1	150,722,453 (GRCm38)	missense	possibly damaging	0.88
R4026:Hmcn1	UTSW	1	150,722,369 (GRCm38)	missense	probably benign	0.03
R4037:Hmcn1	UTSW	1	150,772,502 (GRCm38)	missense	probably benign	0.00
R4088:Hmcn1	UTSW	1	150,703,216 (GRCm38)	missense	possibly damaging	0.58
R4096:Hmcn1	UTSW	1	150,658,508 (GRCm38)	missense	probably benign	0.20
R4169:Hmcn1	UTSW	1	150,595,999 (GRCm38)	splice site	probably null
R4441:Hmcn1	UTSW	1	150,657,459 (GRCm38)	missense	probably null
R4493:Hmcn1	UTSW	1	150,701,899 (GRCm38)	missense	probably damaging	1.00
R4501:Hmcn1	UTSW	1	150,633,666 (GRCm38)	missense	probably damaging	1.00
R4535:Hmcn1	UTSW	1	150,563,780 (GRCm38)	missense	probably damaging	0.99
R4576:Hmcn1	UTSW	1	150,734,487 (GRCm38)	missense	probably benign
R4601:Hmcn1	UTSW	1	150,738,645 (GRCm38)	missense	probably damaging	0.99
R4627:Hmcn1	UTSW	1	150,595,894 (GRCm38)	missense	probably benign	0.11
R4647:Hmcn1	UTSW	1	150,675,511 (GRCm38)	critical splice donor site	probably null
R4657:Hmcn1	UTSW	1	150,624,550 (GRCm38)	missense	probably damaging	1.00
R4717:Hmcn1	UTSW	1	150,619,065 (GRCm38)	missense	probably benign	0.00
R4721:Hmcn1	UTSW	1	150,772,571 (GRCm38)	splice site	probably null
R4724:Hmcn1	UTSW	1	150,694,833 (GRCm38)	splice site	probably null
R4737:Hmcn1	UTSW	1	150,689,595 (GRCm38)	missense	possibly damaging	0.90
R4744:Hmcn1	UTSW	1	150,577,612 (GRCm38)	missense	probably damaging	1.00
R4795:Hmcn1	UTSW	1	150,753,611 (GRCm38)	missense	probably benign	0.00
R4796:Hmcn1	UTSW	1	150,753,611 (GRCm38)	missense	probably benign	0.00
R4871:Hmcn1	UTSW	1	150,593,085 (GRCm38)	missense	probably benign	0.02
R4895:Hmcn1	UTSW	1	150,677,379 (GRCm38)	missense	probably benign	0.00
R4934:Hmcn1	UTSW	1	150,722,535 (GRCm38)	missense	probably damaging	1.00
R4953:Hmcn1	UTSW	1	150,876,360 (GRCm38)	intron	probably benign
R4968:Hmcn1	UTSW	1	150,657,470 (GRCm38)	missense	possibly damaging	0.67
R4974:Hmcn1	UTSW	1	150,819,449 (GRCm38)	missense	probably benign	0.01
R5024:Hmcn1	UTSW	1	150,680,688 (GRCm38)	missense	possibly damaging	0.65
R5031:Hmcn1	UTSW	1	150,588,257 (GRCm38)	missense	probably damaging	1.00
R5093:Hmcn1	UTSW	1	150,737,256 (GRCm38)	missense	probably benign	0.14
R5096:Hmcn1	UTSW	1	150,610,669 (GRCm38)	missense	probably damaging	1.00
R5185:Hmcn1	UTSW	1	150,656,741 (GRCm38)	missense	probably benign	0.03
R5228:Hmcn1	UTSW	1	150,646,701 (GRCm38)	missense	probably benign	0.00
R5260:Hmcn1	UTSW	1	150,595,861 (GRCm38)	missense	possibly damaging	0.65
R5264:Hmcn1	UTSW	1	150,679,514 (GRCm38)	missense	probably benign	0.01
R5282:Hmcn1	UTSW	1	150,582,296 (GRCm38)	missense	probably damaging	1.00
R5334:Hmcn1	UTSW	1	150,755,372 (GRCm38)	missense	probably damaging	0.99
R5346:Hmcn1	UTSW	1	150,623,244 (GRCm38)	missense	probably damaging	1.00
R5423:Hmcn1	UTSW	1	150,701,972 (GRCm38)	missense	probably damaging	1.00
R5484:Hmcn1	UTSW	1	150,675,540 (GRCm38)	missense	probably benign	0.00
R5491:Hmcn1	UTSW	1	150,609,825 (GRCm38)	splice site	probably null
R5531:Hmcn1	UTSW	1	150,743,788 (GRCm38)	missense	probably damaging	1.00
R5536:Hmcn1	UTSW	1	150,755,291 (GRCm38)	missense	probably benign	0.01
R5547:Hmcn1	UTSW	1	150,737,506 (GRCm38)	missense	possibly damaging	0.64
R5580:Hmcn1	UTSW	1	150,577,539 (GRCm38)	missense	probably benign	0.43
R5626:Hmcn1	UTSW	1	150,656,567 (GRCm38)	missense	probably damaging	1.00
R5657:Hmcn1	UTSW	1	150,658,562 (GRCm38)	missense	probably benign	0.02
R5677:Hmcn1	UTSW	1	150,609,778 (GRCm38)	missense	probably benign	0.00
R5718:Hmcn1	UTSW	1	150,690,600 (GRCm38)	nonsense	probably null
R5718:Hmcn1	UTSW	1	150,609,666 (GRCm38)	missense	probably damaging	1.00
R5723:Hmcn1	UTSW	1	150,694,849 (GRCm38)	missense	possibly damaging	0.95
R5739:Hmcn1	UTSW	1	150,758,474 (GRCm38)	splice site	probably null
R5739:Hmcn1	UTSW	1	150,808,697 (GRCm38)	missense	probably benign	0.45
R5751:Hmcn1	UTSW	1	150,573,554 (GRCm38)	missense	probably damaging	1.00
R5772:Hmcn1	UTSW	1	150,694,878 (GRCm38)	missense	possibly damaging	0.47
R5804:Hmcn1	UTSW	1	150,674,347 (GRCm38)	nonsense	probably null
R5809:Hmcn1	UTSW	1	150,649,607 (GRCm38)	missense	probably damaging	1.00
R5817:Hmcn1	UTSW	1	150,737,524 (GRCm38)	missense	possibly damaging	0.77
R5824:Hmcn1	UTSW	1	150,993,023 (GRCm38)	missense	probably benign	0.12
R5881:Hmcn1	UTSW	1	150,630,327 (GRCm38)	missense	probably damaging	0.99
R5928:Hmcn1	UTSW	1	150,598,897 (GRCm38)	missense	possibly damaging	0.64
R5929:Hmcn1	UTSW	1	150,577,296 (GRCm38)	nonsense	probably null
R5940:Hmcn1	UTSW	1	150,657,222 (GRCm38)	missense	probably benign	0.41
R5973:Hmcn1	UTSW	1	150,563,817 (GRCm38)	missense	probably damaging	1.00
R5997:Hmcn1	UTSW	1	150,704,173 (GRCm38)	missense	possibly damaging	0.74
R6027:Hmcn1	UTSW	1	150,802,895 (GRCm38)	missense	possibly damaging	0.79
R6029:Hmcn1	UTSW	1	150,632,437 (GRCm38)	missense	probably benign	0.13
R6056:Hmcn1	UTSW	1	150,663,909 (GRCm38)	missense	probably damaging	1.00
R6065:Hmcn1	UTSW	1	150,770,330 (GRCm38)	missense	probably benign	0.06
R6083:Hmcn1	UTSW	1	150,755,294 (GRCm38)	missense	probably damaging	1.00
R6083:Hmcn1	UTSW	1	150,755,293 (GRCm38)	missense	probably damaging	1.00
R6108:Hmcn1	UTSW	1	150,631,227 (GRCm38)	missense	possibly damaging	0.95
R6112:Hmcn1	UTSW	1	150,618,936 (GRCm38)	missense	probably damaging	1.00
R6140:Hmcn1	UTSW	1	150,732,846 (GRCm38)	missense	probably damaging	1.00
R6144:Hmcn1	UTSW	1	150,722,424 (GRCm38)	missense	probably damaging	1.00
R6152:Hmcn1	UTSW	1	150,565,425 (GRCm38)	missense	probably damaging	1.00
R6174:Hmcn1	UTSW	1	150,646,784 (GRCm38)	missense	probably benign	0.06
R6185:Hmcn1	UTSW	1	150,615,438 (GRCm38)	splice site	probably null
R6187:Hmcn1	UTSW	1	150,630,728 (GRCm38)	missense	probably damaging	1.00
R6276:Hmcn1	UTSW	1	150,738,681 (GRCm38)	missense	possibly damaging	0.69
R6278:Hmcn1	UTSW	1	150,697,419 (GRCm38)	critical splice donor site	probably null
R6427:Hmcn1	UTSW	1	150,697,476 (GRCm38)	missense	possibly damaging	0.85
R6431:Hmcn1	UTSW	1	150,744,960 (GRCm38)	missense	probably benign	0.01
R6441:Hmcn1	UTSW	1	150,703,216 (GRCm38)	missense	possibly damaging	0.58
R6451:Hmcn1	UTSW	1	150,992,919 (GRCm38)	missense	probably damaging	1.00
R6478:Hmcn1	UTSW	1	150,664,784 (GRCm38)	missense	probably damaging	1.00
R6479:Hmcn1	UTSW	1	150,677,302 (GRCm38)	nonsense	probably null
R6490:Hmcn1	UTSW	1	150,583,278 (GRCm38)	missense	probably benign	0.00
R6525:Hmcn1	UTSW	1	150,697,566 (GRCm38)	missense	probably damaging	1.00
R6571:Hmcn1	UTSW	1	150,615,438 (GRCm38)	splice site	probably null
R6612:Hmcn1	UTSW	1	150,595,118 (GRCm38)	critical splice donor site	probably null
R6616:Hmcn1	UTSW	1	150,723,257 (GRCm38)	critical splice donor site	probably null
R6617:Hmcn1	UTSW	1	150,743,796 (GRCm38)	missense	probably benign	0.01
R6623:Hmcn1	UTSW	1	150,758,306 (GRCm38)	missense	probably benign
R6687:Hmcn1	UTSW	1	150,745,033 (GRCm38)	missense	probably benign	0.30
R6714:Hmcn1	UTSW	1	150,704,175 (GRCm38)	missense	probably damaging	0.97
R6751:Hmcn1	UTSW	1	150,734,518 (GRCm38)	missense	probably damaging	0.98
R6831:Hmcn1	UTSW	1	150,770,293 (GRCm38)	missense	probably benign	0.00
R6971:Hmcn1	UTSW	1	150,993,051 (GRCm38)	start codon destroyed	probably benign	0.00
R7048:Hmcn1	UTSW	1	150,599,653 (GRCm38)	critical splice acceptor site	probably null
R7058:Hmcn1	UTSW	1	150,773,890 (GRCm38)	missense	probably benign	0.43
R7071:Hmcn1	UTSW	1	150,604,102 (GRCm38)	missense	probably damaging	1.00
R7078:Hmcn1	UTSW	1	150,860,367 (GRCm38)	missense	probably damaging	1.00
R7092:Hmcn1	UTSW	1	150,604,246 (GRCm38)	missense	probably damaging	1.00
R7120:Hmcn1	UTSW	1	150,700,541 (GRCm38)	missense	probably damaging	0.98
R7129:Hmcn1	UTSW	1	150,577,210 (GRCm38)	splice site	probably null
R7144:Hmcn1	UTSW	1	150,663,873 (GRCm38)	missense	probably damaging	1.00
R7148:Hmcn1	UTSW	1	150,686,854 (GRCm38)	missense	probably benign	0.00
R7162:Hmcn1	UTSW	1	150,748,993 (GRCm38)	missense	probably benign	0.18
R7172:Hmcn1	UTSW	1	150,753,699 (GRCm38)	missense	possibly damaging	0.92
R7193:Hmcn1	UTSW	1	150,649,580 (GRCm38)	missense	probably null	1.00
R7231:Hmcn1	UTSW	1	150,638,876 (GRCm38)	missense	probably benign	0.00
R7237:Hmcn1	UTSW	1	150,722,643 (GRCm38)	missense	probably damaging	0.98
R7258:Hmcn1	UTSW	1	150,715,823 (GRCm38)	missense	probably benign	0.12
R7286:Hmcn1	UTSW	1	150,582,337 (GRCm38)	missense	probably damaging	0.98
R7289:Hmcn1	UTSW	1	150,683,715 (GRCm38)	missense	possibly damaging	0.52
R7292:Hmcn1	UTSW	1	150,733,129 (GRCm38)	splice site	probably null
R7316:Hmcn1	UTSW	1	150,732,946 (GRCm38)	missense	probably damaging	1.00
R7327:Hmcn1	UTSW	1	150,603,814 (GRCm38)	missense	probably benign	0.01
R7328:Hmcn1	UTSW	1	150,638,866 (GRCm38)	missense	possibly damaging	0.95
R7346:Hmcn1	UTSW	1	150,683,745 (GRCm38)	missense	probably damaging	1.00
R7351:Hmcn1	UTSW	1	150,667,889 (GRCm38)	missense	probably damaging	0.98
R7354:Hmcn1	UTSW	1	150,806,445 (GRCm38)	nonsense	probably null
R7360:Hmcn1	UTSW	1	150,618,846 (GRCm38)	missense	probably damaging	1.00
R7396:Hmcn1	UTSW	1	150,563,631 (GRCm38)	missense	possibly damaging	0.83
R7398:Hmcn1	UTSW	1	150,646,670 (GRCm38)	missense	probably benign	0.00
R7400:Hmcn1	UTSW	1	150,674,430 (GRCm38)	missense	probably damaging	1.00
R7404:Hmcn1	UTSW	1	150,720,759 (GRCm38)	missense	probably benign	0.00
R7424:Hmcn1	UTSW	1	150,630,266 (GRCm38)	nonsense	probably null
R7454:Hmcn1	UTSW	1	150,563,604 (GRCm38)	missense	probably damaging	1.00
R7476:Hmcn1	UTSW	1	150,580,267 (GRCm38)	missense	probably damaging	0.99
R7480:Hmcn1	UTSW	1	150,677,234 (GRCm38)	critical splice donor site	probably null
R7516:Hmcn1	UTSW	1	150,622,967 (GRCm38)	missense	probably benign	0.35
R7526:Hmcn1	UTSW	1	150,656,573 (GRCm38)	missense	probably damaging	1.00
R7531:Hmcn1	UTSW	1	150,686,780 (GRCm38)	missense	probably benign	0.06
R7555:Hmcn1	UTSW	1	150,604,874 (GRCm38)	missense	probably benign	0.40
R7564:Hmcn1	UTSW	1	150,655,835 (GRCm38)	missense	probably benign
R7588:Hmcn1	UTSW	1	150,657,134 (GRCm38)	missense	possibly damaging	0.90
R7719:Hmcn1	UTSW	1	150,565,329 (GRCm38)	missense	possibly damaging	0.95
R7720:Hmcn1	UTSW	1	150,646,709 (GRCm38)	missense	probably benign	0.00
R7722:Hmcn1	UTSW	1	150,667,880 (GRCm38)	missense	probably damaging	0.98
R7761:Hmcn1	UTSW	1	150,722,445 (GRCm38)	missense	possibly damaging	0.70
R7787:Hmcn1	UTSW	1	150,756,592 (GRCm38)	missense	probably damaging	1.00
R7803:Hmcn1	UTSW	1	150,770,279 (GRCm38)	missense	probably benign	0.32
R7862:Hmcn1	UTSW	1	150,806,421 (GRCm38)	missense	probably damaging	0.96
R7876:Hmcn1	UTSW	1	150,744,971 (GRCm38)	missense	probably benign	0.03
R7886:Hmcn1	UTSW	1	150,657,470 (GRCm38)	missense	possibly damaging	0.94
R7891:Hmcn1	UTSW	1	150,593,189 (GRCm38)	missense	probably damaging	1.00
R7892:Hmcn1	UTSW	1	150,664,892 (GRCm38)	missense	probably benign	0.00
R7927:Hmcn1	UTSW	1	150,609,775 (GRCm38)	missense	probably damaging	1.00
R7941:Hmcn1	UTSW	1	150,650,084 (GRCm38)	missense	possibly damaging	0.95
R7960:Hmcn1	UTSW	1	150,655,855 (GRCm38)	missense	probably damaging	1.00
R8001:Hmcn1	UTSW	1	150,664,878 (GRCm38)	nonsense	probably null
R8015:Hmcn1	UTSW	1	150,598,311 (GRCm38)	missense	possibly damaging	0.83
R8070:Hmcn1	UTSW	1	150,649,992 (GRCm38)	nonsense	probably null
R8072:Hmcn1	UTSW	1	150,656,505 (GRCm38)	missense	possibly damaging	0.62
R8113:Hmcn1	UTSW	1	150,749,090 (GRCm38)	missense	possibly damaging	0.50
R8143:Hmcn1	UTSW	1	150,859,206 (GRCm38)	missense	probably benign	0.03
R8145:Hmcn1	UTSW	1	150,753,660 (GRCm38)	missense	probably benign	0.33
R8155:Hmcn1	UTSW	1	150,604,954 (GRCm38)	missense	probably damaging	1.00
R8165:Hmcn1	UTSW	1	150,646,658 (GRCm38)	missense	probably benign	0.09
R8179:Hmcn1	UTSW	1	150,722,514 (GRCm38)	missense	probably benign	0.19
R8193:Hmcn1	UTSW	1	150,577,477 (GRCm38)	nonsense	probably null
R8234:Hmcn1	UTSW	1	150,594,010 (GRCm38)	missense	possibly damaging	0.83
R8249:Hmcn1	UTSW	1	150,819,366 (GRCm38)	missense	probably benign	0.24
R8267:Hmcn1	UTSW	1	150,859,254 (GRCm38)	missense	probably damaging	1.00
R8312:Hmcn1	UTSW	1	150,738,764 (GRCm38)	missense	probably damaging	0.99
R8338:Hmcn1	UTSW	1	150,738,734 (GRCm38)	missense	probably benign	0.35
R8354:Hmcn1	UTSW	1	150,758,391 (GRCm38)	missense	possibly damaging	0.79
R8440:Hmcn1	UTSW	1	150,694,920 (GRCm38)	missense	probably damaging	1.00
R8473:Hmcn1	UTSW	1	150,603,800 (GRCm38)	missense	possibly damaging	0.64
R8497:Hmcn1	UTSW	1	150,580,239 (GRCm38)	missense	probably benign	0.01
R8509:Hmcn1	UTSW	1	150,573,551 (GRCm38)	nonsense	probably null
R8559:Hmcn1	UTSW	1	150,676,038 (GRCm38)	missense	probably benign	0.25
R8701:Hmcn1	UTSW	1	150,755,257 (GRCm38)	missense	probably benign	0.00
R8755:Hmcn1	UTSW	1	150,633,620 (GRCm38)	missense	probably benign	0.19
R8765:Hmcn1	UTSW	1	150,680,662 (GRCm38)	missense	probably damaging	0.98
R8782:Hmcn1	UTSW	1	150,664,885 (GRCm38)	missense	probably benign	0.08
R8794:Hmcn1	UTSW	1	150,715,718 (GRCm38)	missense	probably benign	0.00
R8803:Hmcn1	UTSW	1	150,734,497 (GRCm38)	missense	probably damaging	1.00
R8808:Hmcn1	UTSW	1	150,655,819 (GRCm38)	missense	possibly damaging	0.64
R8853:Hmcn1	UTSW	1	150,671,975 (GRCm38)	missense	probably damaging	1.00
R8877:Hmcn1	UTSW	1	150,638,908 (GRCm38)	missense	probably benign	0.00
R8881:Hmcn1	UTSW	1	150,649,972 (GRCm38)	missense	probably damaging	1.00
R8916:Hmcn1	UTSW	1	150,773,779 (GRCm38)	missense	probably damaging	1.00
R9008:Hmcn1	UTSW	1	150,755,044 (GRCm38)	intron	probably benign
R9030:Hmcn1	UTSW	1	150,817,119 (GRCm38)	missense	probably benign	0.00
R9072:Hmcn1	UTSW	1	150,689,569 (GRCm38)	missense	probably benign	0.04
R9090:Hmcn1	UTSW	1	150,756,558 (GRCm38)	missense	probably damaging	1.00
R9096:Hmcn1	UTSW	1	150,657,118 (GRCm38)	missense	probably benign	0.04
R9102:Hmcn1	UTSW	1	150,697,580 (GRCm38)	missense	probably benign	0.01
R9146:Hmcn1	UTSW	1	150,598,390 (GRCm38)	missense	probably benign	0.02
R9157:Hmcn1	UTSW	1	150,646,592 (GRCm38)	missense	probably benign	0.06
R9169:Hmcn1	UTSW	1	150,630,341 (GRCm38)	missense	probably damaging	0.99
R9182:Hmcn1	UTSW	1	150,612,654 (GRCm38)	missense	probably damaging	1.00
R9182:Hmcn1	UTSW	1	150,624,586 (GRCm38)	nonsense	probably null
R9204:Hmcn1	UTSW	1	150,734,511 (GRCm38)	missense	probably benign	0.40
R9219:Hmcn1	UTSW	1	150,719,093 (GRCm38)	critical splice donor site	probably null
R9267:Hmcn1	UTSW	1	150,597,989 (GRCm38)	missense	probably benign	0.26
R9271:Hmcn1	UTSW	1	150,756,558 (GRCm38)	missense	probably damaging	1.00
R9274:Hmcn1	UTSW	1	150,630,295 (GRCm38)	missense	probably benign	0.01
R9313:Hmcn1	UTSW	1	150,646,592 (GRCm38)	missense	probably benign	0.06
R9414:Hmcn1	UTSW	1	150,669,436 (GRCm38)	missense	probably damaging	1.00
R9456:Hmcn1	UTSW	1	150,630,302 (GRCm38)	nonsense	probably null
R9464:Hmcn1	UTSW	1	150,723,497 (GRCm38)	missense	possibly damaging	0.80
R9474:Hmcn1	UTSW	1	150,630,720 (GRCm38)	missense	probably damaging	1.00
R9476:Hmcn1	UTSW	1	150,586,376 (GRCm38)	missense	probably benign	0.00
R9482:Hmcn1	UTSW	1	150,734,530 (GRCm38)	missense	probably benign	0.06
R9496:Hmcn1	UTSW	1	150,704,220 (GRCm38)	missense	probably benign	0.00
R9501:Hmcn1	UTSW	1	150,595,239 (GRCm38)	missense	possibly damaging	0.67
R9510:Hmcn1	UTSW	1	150,586,376 (GRCm38)	missense	probably benign	0.00
R9529:Hmcn1	UTSW	1	150,669,424 (GRCm38)	missense	probably damaging	1.00
R9566:Hmcn1	UTSW	1	150,622,909 (GRCm38)	missense	probably benign	0.00
R9608:Hmcn1	UTSW	1	150,599,552 (GRCm38)	missense	probably damaging	1.00
R9609:Hmcn1	UTSW	1	150,679,595 (GRCm38)	missense	probably damaging	0.96
R9616:Hmcn1	UTSW	1	150,808,722 (GRCm38)	missense	probably benign	0.16
R9627:Hmcn1	UTSW	1	150,630,303 (GRCm38)	missense	probably damaging	1.00
R9668:Hmcn1	UTSW	1	150,743,741 (GRCm38)	missense	probably benign	0.02
R9686:Hmcn1	UTSW	1	150,737,605 (GRCm38)	missense	probably damaging	0.99
R9717:Hmcn1	UTSW	1	150,609,627 (GRCm38)	missense	probably damaging	1.00
R9727:Hmcn1	UTSW	1	150,798,815 (GRCm38)	missense	probably benign	0.06
R9744:Hmcn1	UTSW	1	150,748,190 (GRCm38)	missense	probably damaging	1.00
R9749:Hmcn1	UTSW	1	150,756,588 (GRCm38)	missense	possibly damaging	0.94
R9761:Hmcn1	UTSW	1	150,992,874 (GRCm38)	missense	probably damaging	0.98
R9783:Hmcn1	UTSW	1	150,722,629 (GRCm38)	missense	probably benign	0.16
R9788:Hmcn1	UTSW	1	150,652,582 (GRCm38)	missense	probably benign	0.00
R9792:Hmcn1	UTSW	1	150,732,938 (GRCm38)	missense	possibly damaging	0.94
R9793:Hmcn1	UTSW	1	150,732,938 (GRCm38)	missense	possibly damaging	0.94
R9795:Hmcn1	UTSW	1	150,732,938 (GRCm38)	missense	possibly damaging	0.94
R9802:Hmcn1	UTSW	1	150,808,640 (GRCm38)	missense	probably benign	0.07
RF003:Hmcn1	UTSW	1	150,624,561 (GRCm38)	missense	probably damaging	1.00
RF005:Hmcn1	UTSW	1	150,635,146 (GRCm38)	nonsense	probably null
X0022:Hmcn1	UTSW	1	150,700,530 (GRCm38)	missense	probably benign	0.04
X0027:Hmcn1	UTSW	1	150,860,376 (GRCm38)	missense	probably damaging	1.00
X0028:Hmcn1	UTSW	1	150,663,901 (GRCm38)	missense	probably damaging	1.00
Z1088:Hmcn1	UTSW	1	150,648,937 (GRCm38)	missense	probably damaging	1.00
Z1176:Hmcn1	UTSW	1	150,663,917 (GRCm38)	missense	probably benign	0.12
Z1176:Hmcn1	UTSW	1	150,655,921 (GRCm38)	missense	possibly damaging	0.65
Z1176:Hmcn1	UTSW	1	150,586,445 (GRCm38)	missense	probably null	0.92

Predicted Primers

PCR Primer
(F):5'- TTCCTGCTACATTCACAGCAAC -3'
(R):5'- TGATCATGCAGTCTGCTGTC -3'

Sequencing Primer
(F):5'- CACACACATAACGGCCGGTG -3'
(R):5'- AGGTGGCACATTCCCATTG -3'

Posted On

2014-12-04