Mutagenetix > Incidental Mutation

Incidental Mutation 'R7527:Csmd1'

583067

Institutional Source

Beutler Lab

Gene Symbol

Csmd1

Ensembl Gene

ENSMUSG00000060924

Gene Name

CUB and Sushi multiple domains 1

Synonyms

MMRRC Submission

045599-MU

Accession Numbers

Genbank: NM_053171.2

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7527 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

15892537-17535586 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 16211718 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Threonine at position 922 (A922T)

Ref Sequence

ENSEMBL: ENSMUSP00000080751 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000082104]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000082104
AA Change: A922T

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000080751
Gene: ENSMUSG00000060924
AA Change: A922T

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
CUB	32	140	1.46e-26	SMART
CCP	145	202	1.01e-11	SMART
CUB	208	312	1.05e-27	SMART
CCP	349	406	1.28e-8	SMART
CUB	411	522	2.34e-25	SMART
CCP	527	580	1.22e-14	SMART
CUB	584	692	1.61e-37	SMART
CCP	697	754	4.41e-12	SMART
CUB	758	866	6.55e-38	SMART
CCP	873	926	2.53e-12	SMART
CUB	930	1040	8.94e-22	SMART
CCP	1045	1100	7.06e-11	SMART
CUB	1104	1212	3.14e-26	SMART
CCP	1217	1273	1.18e-12	SMART
CUB	1277	1386	9.72e-32	SMART
CCP	1391	1447	2.06e-12	SMART
CUB	1451	1559	1.68e-35	SMART
CCP	1564	1621	2.53e-12	SMART
CUB	1625	1733	4.24e-14	SMART
CCP	1741	1798	9.46e-12	SMART
CUB	1802	1910	4.23e-32	SMART
CCP	1915	1970	8.23e-12	SMART
CUB	1974	2082	8.59e-33	SMART
CCP	2087	2142	6.09e-15	SMART
CUB	2146	2253	2.36e-30	SMART
CCP	2258	2315	1.1e-12	SMART
CUB	2320	2430	4.3e-24	SMART
CCP	2432	2490	2.94e-8	SMART
CCP	2495	2552	2.03e-11	SMART
CCP	2557	2617	1.22e-5	SMART
CCP	2622	2675	2.72e-12	SMART
CCP	2680	2733	5.86e-17	SMART
CCP	2738	2791	6.09e-15	SMART
CCP	2796	2854	9.1e-14	SMART
CCP	2859	2912	3.96e-14	SMART
CCP	2920	2973	4.41e-12	SMART
CCP	2978	3032	2.94e-8	SMART
CCP	3037	3092	6.59e-11	SMART
CCP	3097	3150	4.12e-12	SMART
CCP	3155	3208	7.92e-14	SMART
CCP	3216	3270	2.8e-14	SMART
CCP	3275	3330	3.78e-11	SMART
transmembrane domain	3487	3509	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice exhibit normal pre-pulse inhibition, social interaction, sucrose preference and d-amphetamine sensitivity. [provided by MGI curators]

Allele List at MGI

All alleles(1) : Targeted, knock-out(1)

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5730559C18Rik	T	A	1: 136,214,384 (GRCm38)	D659V	possibly damaging	Het
Abca5	A	T	11: 110,327,730 (GRCm38)		probably null	Het
Abcc10	A	G	17: 46,312,904 (GRCm38)	S810P	possibly damaging	Het
Adam22	T	C	5: 8,082,239 (GRCm38)	H138R	possibly damaging	Het
Adcyap1	T	A	17: 93,202,829 (GRCm38)	L95*	probably null	Het
Adgrl4	C	A	3: 151,439,250 (GRCm38)	T12N	probably benign	Het
Alpi	T	C	1: 87,098,955 (GRCm38)	N438S	probably benign	Het
Ankrd44	T	C	1: 54,648,324 (GRCm38)	N979D	probably benign	Het
Ankrd60	A	C	2: 173,578,173 (GRCm38)	S57A	probably benign	Het
Arfgef3	G	A	10: 18,646,629 (GRCm38)	P550S	probably benign	Het
Btbd16	A	T	7: 130,820,472 (GRCm38)	D390V	probably damaging	Het
Cacna2d4	T	C	6: 119,271,247 (GRCm38)	V374A	probably benign	Het
Cdcp1	A	T	9: 123,185,107 (GRCm38)	F201I	probably benign	Het
Cdh15	A	T	8: 122,862,126 (GRCm38)	D313V	probably damaging	Het
Cfap157	A	G	2: 32,779,878 (GRCm38)	L231P	possibly damaging	Het
Chl1	T	G	6: 103,711,201 (GRCm38)	C1001G	probably damaging	Het
Cmtr2	A	G	8: 110,222,138 (GRCm38)	H360R	probably damaging	Het
Fam129c	C	G	8: 71,606,698 (GRCm38)	C568W	probably damaging	Het
Fancg	C	T	4: 43,010,116 (GRCm38)		probably benign	Het
Glt8d2	A	T	10: 82,652,569 (GRCm38)	S356T	unknown	Het
Gm19410	T	A	8: 35,802,232 (GRCm38)	C1074S	probably damaging	Het
Gm3259	A	G	5: 95,342,550 (GRCm38)	D347G	probably benign	Het
Gm9195	C	T	14: 72,473,870 (GRCm38)	C376Y	possibly damaging	Het
Gnai3	G	A	3: 108,118,377 (GRCm38)	R129C		Het
Golph3	T	G	15: 12,343,318 (GRCm38)		probably null	Het
Hist2h2bb	T	A	3: 96,269,870 (GRCm38)	V40D	possibly damaging	Het
Hk1	C	A	10: 62,304,782 (GRCm38)	V105F	probably damaging	Het
Hoxd8	A	G	2: 74,705,657 (GRCm38)	Y37C	probably damaging	Het
Jun	G	T	4: 95,050,997 (GRCm38)	P92Q	probably damaging	Het
Klhl14	C	T	18: 21,651,540 (GRCm38)	V277I	probably damaging	Het
Lrrc51	C	T	7: 101,920,636 (GRCm38)		probably null	Het
Man2c1	T	A	9: 57,137,816 (GRCm38)	Y429*	probably null	Het
Myo18a	T	A	11: 77,843,580 (GRCm38)	C1476S	probably benign	Het
Neb	G	C	2: 52,176,623 (GRCm38)	T6155R	probably damaging	Het
Nuf2	T	C	1: 169,498,853 (GRCm38)	E443G	possibly damaging	Het
Olfr1164	A	T	2: 88,093,610 (GRCm38)	C109S	probably damaging	Het
Olfr1211	A	G	2: 88,930,090 (GRCm38)	V75A	probably benign	Het
Olfr16	C	T	1: 172,956,944 (GRCm38)	H50Y	probably benign	Het
Olfr851	A	G	9: 19,497,389 (GRCm38)	I214V	probably damaging	Het
Osmr	A	G	15: 6,827,122 (GRCm38)	S515P	probably damaging	Het
Pik3r5	T	C	11: 68,476,351 (GRCm38)	L84P	probably damaging	Het
Plcl1	T	C	1: 55,697,114 (GRCm38)	I538T	probably damaging	Het
Plxnb1	G	T	9: 109,100,861 (GRCm38)	V262L	probably damaging	Het
Pprc1	T	C	19: 46,069,365 (GRCm38)	S1320P	unknown	Het
Prap1	G	A	7: 140,096,207 (GRCm38)		probably null	Het
Psg23	A	T	7: 18,614,774 (GRCm38)	V36D	probably damaging	Het
Ptgr1	A	G	4: 58,982,887 (GRCm38)	Y49H	probably damaging	Het
Ptprr	A	G	10: 116,251,199 (GRCm38)	T528A	probably benign	Het
Rapgef6	T	C	11: 54,634,961 (GRCm38)	S541P	unknown	Het
Rnf17	A	T	14: 56,516,438 (GRCm38)	D1534V	probably damaging	Het
Sdk1	T	G	5: 141,792,976 (GRCm38)	S236R	possibly damaging	Het
Sepsecs	A	G	5: 52,644,051 (GRCm38)	M423T	possibly damaging	Het
Serpina1f	T	G	12: 103,691,908 (GRCm38)	Y246S	probably benign	Het
Sftpb	T	A	6: 72,305,064 (GRCm38)	V46E	possibly damaging	Het
Slc4a1ap	G	A	5: 31,534,131 (GRCm38)	V424I	probably benign	Het
Slc5a4b	G	A	10: 76,110,908 (GRCm38)	T10M	probably benign	Het
Slc6a16	T	C	7: 45,272,639 (GRCm38)	W664R	probably damaging	Het
Snx8	T	C	5: 140,356,072 (GRCm38)	E138G	probably benign	Het
Sox6	T	C	7: 115,777,173 (GRCm38)	E108G	probably benign	Het
Sptan1	A	T	2: 29,980,197 (GRCm38)	I120F	probably damaging	Het
Sptbn4	T	C	7: 27,375,590 (GRCm38)	E1452G	possibly damaging	Het
Stac2	T	A	11: 98,039,626 (GRCm38)	E372V	probably damaging	Het
Taco1	A	T	11: 106,071,969 (GRCm38)	I161F	probably damaging	Het
Taf1d	C	A	9: 15,308,837 (GRCm38)	D127E	possibly damaging	Het
Tenm2	T	A	11: 36,206,976 (GRCm38)	N482Y	probably damaging	Het
Tenm3	A	G	8: 48,276,600 (GRCm38)	V1457A	possibly damaging	Het
Tmem200c	A	T	17: 68,841,676 (GRCm38)	H418L	probably benign	Het
Tmem81	T	C	1: 132,508,146 (GRCm38)	V230A	probably benign	Het
Tnn	C	T	1: 160,118,504 (GRCm38)	V915I	possibly damaging	Het
Trav8d-2	A	T	14: 53,042,697 (GRCm38)	Y48F	possibly damaging	Het
Trpm2	T	C	10: 77,966,060 (GRCm38)	N57S	probably benign	Het
Ttn	G	A	2: 76,768,039 (GRCm38)	T19510M	probably damaging	Het
Ubl7	T	C	9: 57,912,884 (GRCm38)	L73P	unknown	Het
Uso1	A	G	5: 92,199,875 (GRCm38)	D845G	possibly damaging	Het
Utrn	G	T	10: 12,401,382 (GRCm38)	P3397Q	possibly damaging	Het
Vmn2r60	AG	A	7: 42,195,734 (GRCm38)		probably null	Het

Other mutations in Csmd1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00095:Csmd1	APN	8	16,009,297 (GRCm38)	splice site	probably benign
IGL00433:Csmd1	APN	8	16,231,373 (GRCm38)	missense	probably damaging	1.00
IGL00500:Csmd1	APN	8	15,921,139 (GRCm38)	missense	probably damaging	1.00
IGL00666:Csmd1	APN	8	16,189,990 (GRCm38)	missense	probably damaging	1.00
IGL00913:Csmd1	APN	8	16,071,287 (GRCm38)	missense	probably benign	0.00
IGL01012:Csmd1	APN	8	15,917,341 (GRCm38)	missense	probably benign	0.00
IGL01123:Csmd1	APN	8	17,534,928 (GRCm38)	missense	possibly damaging	0.96
IGL01348:Csmd1	APN	8	15,910,596 (GRCm38)	missense	probably damaging	0.99
IGL01444:Csmd1	APN	8	16,200,055 (GRCm38)	missense	probably benign	0.00
IGL01530:Csmd1	APN	8	15,903,195 (GRCm38)	missense	probably damaging	0.99
IGL01548:Csmd1	APN	8	16,288,646 (GRCm38)	nonsense	probably null
IGL01814:Csmd1	APN	8	16,501,375 (GRCm38)	missense	probably damaging	1.00
IGL01889:Csmd1	APN	8	15,998,857 (GRCm38)	missense	probably damaging	1.00
IGL02055:Csmd1	APN	8	16,069,001 (GRCm38)	missense	probably damaging	0.99
IGL02066:Csmd1	APN	8	15,926,594 (GRCm38)	missense	probably damaging	1.00
IGL02097:Csmd1	APN	8	16,211,759 (GRCm38)	missense	probably null	0.17
IGL02112:Csmd1	APN	8	16,081,705 (GRCm38)	missense	probably benign	0.18
IGL02161:Csmd1	APN	8	16,358,412 (GRCm38)	missense	probably damaging	0.97
IGL02189:Csmd1	APN	8	16,271,606 (GRCm38)	missense	probably damaging	0.99
IGL02272:Csmd1	APN	8	16,199,893 (GRCm38)	missense	probably damaging	0.99
IGL02292:Csmd1	APN	8	16,211,870 (GRCm38)	missense	probably damaging	1.00
IGL02385:Csmd1	APN	8	15,903,275 (GRCm38)	missense	probably benign	0.08
IGL02424:Csmd1	APN	8	16,092,326 (GRCm38)	missense	probably benign	0.22
IGL02492:Csmd1	APN	8	16,002,597 (GRCm38)	missense	probably benign	0.13
IGL02507:Csmd1	APN	8	17,534,976 (GRCm38)	utr 5 prime	probably benign
IGL02513:Csmd1	APN	8	15,999,869 (GRCm38)	splice site	probably benign
IGL02727:Csmd1	APN	8	16,231,327 (GRCm38)	missense	probably damaging	1.00
IGL02728:Csmd1	APN	8	15,999,779 (GRCm38)	critical splice donor site	probably null
IGL02852:Csmd1	APN	8	15,895,728 (GRCm38)	missense	probably damaging	0.99
IGL02935:Csmd1	APN	8	16,223,334 (GRCm38)	missense	probably damaging	1.00
IGL02945:Csmd1	APN	8	16,271,570 (GRCm38)	missense	possibly damaging	0.92
IGL02959:Csmd1	APN	8	15,910,465 (GRCm38)	missense	probably damaging	0.99
IGL03113:Csmd1	APN	8	16,028,698 (GRCm38)	missense	probably benign
IGL03129:Csmd1	APN	8	15,961,521 (GRCm38)	missense	probably damaging	0.99
IGL03131:Csmd1	APN	8	16,088,217 (GRCm38)	missense	probably damaging	1.00
IGL03275:Csmd1	APN	8	16,157,092 (GRCm38)	missense	probably benign	0.00
IGL03297:Csmd1	APN	8	16,009,432 (GRCm38)	nonsense	probably null
ikura	UTSW	8	16,231,271 (GRCm38)	missense	probably damaging	1.00
I2289:Csmd1	UTSW	8	15,912,381 (GRCm38)	missense	probably benign	0.10
IGL03055:Csmd1	UTSW	8	16,095,501 (GRCm38)	missense	probably damaging	1.00
IGL03097:Csmd1	UTSW	8	15,945,127 (GRCm38)	missense	probably damaging	1.00
PIT4260001:Csmd1	UTSW	8	16,070,313 (GRCm38)	missense	probably damaging	1.00
PIT4378001:Csmd1	UTSW	8	15,895,728 (GRCm38)	missense	probably damaging	0.99
PIT4520001:Csmd1	UTSW	8	15,906,023 (GRCm38)	missense	probably benign	0.01
R0037:Csmd1	UTSW	8	15,917,248 (GRCm38)	missense	probably damaging	0.97
R0095:Csmd1	UTSW	8	16,233,051 (GRCm38)	missense	probably damaging	1.00
R0113:Csmd1	UTSW	8	15,984,849 (GRCm38)	missense	probably damaging	1.00
R0129:Csmd1	UTSW	8	16,079,942 (GRCm38)	missense	possibly damaging	0.95
R0144:Csmd1	UTSW	8	16,391,824 (GRCm38)	missense	probably benign	0.16
R0166:Csmd1	UTSW	8	16,233,022 (GRCm38)	missense	probably benign	0.29
R0227:Csmd1	UTSW	8	16,391,822 (GRCm38)	missense	probably benign	0.05
R0279:Csmd1	UTSW	8	16,223,235 (GRCm38)	missense	probably damaging	0.99
R0280:Csmd1	UTSW	8	16,271,602 (GRCm38)	missense	probably damaging	1.00
R0312:Csmd1	UTSW	8	15,984,760 (GRCm38)	missense	probably damaging	1.00
R0355:Csmd1	UTSW	8	15,918,330 (GRCm38)	missense	probably damaging	0.97
R0367:Csmd1	UTSW	8	15,917,270 (GRCm38)	missense	probably damaging	1.00
R0395:Csmd1	UTSW	8	16,346,638 (GRCm38)	missense	probably damaging	0.99
R0413:Csmd1	UTSW	8	16,710,514 (GRCm38)	missense	probably damaging	0.97
R0457:Csmd1	UTSW	8	16,501,393 (GRCm38)	critical splice acceptor site	probably null
R0463:Csmd1	UTSW	8	15,921,759 (GRCm38)	missense	probably damaging	0.99
R0482:Csmd1	UTSW	8	16,233,101 (GRCm38)	missense	probably damaging	1.00
R0501:Csmd1	UTSW	8	17,027,323 (GRCm38)	missense	probably damaging	0.97
R0505:Csmd1	UTSW	8	15,992,758 (GRCm38)	missense	probably damaging	1.00
R0507:Csmd1	UTSW	8	16,185,344 (GRCm38)	splice site	probably benign
R0511:Csmd1	UTSW	8	15,932,529 (GRCm38)	missense	possibly damaging	0.80
R0555:Csmd1	UTSW	8	16,185,273 (GRCm38)	missense	probably benign
R0580:Csmd1	UTSW	8	15,910,528 (GRCm38)	missense	probably damaging	1.00
R0610:Csmd1	UTSW	8	15,918,208 (GRCm38)	missense	possibly damaging	0.95
R0634:Csmd1	UTSW	8	16,226,391 (GRCm38)	missense	probably damaging	1.00
R0666:Csmd1	UTSW	8	16,069,049 (GRCm38)	missense	possibly damaging	0.88
R0674:Csmd1	UTSW	8	16,000,550 (GRCm38)	missense	probably benign	0.03
R0675:Csmd1	UTSW	8	16,158,131 (GRCm38)	missense	probably benign	0.01
R0763:Csmd1	UTSW	8	17,027,284 (GRCm38)	missense	possibly damaging	0.67
R0781:Csmd1	UTSW	8	15,921,174 (GRCm38)	missense	probably benign	0.35
R0862:Csmd1	UTSW	8	16,190,026 (GRCm38)	missense	probably damaging	0.99
R0864:Csmd1	UTSW	8	16,190,026 (GRCm38)	missense	probably damaging	0.99
R0925:Csmd1	UTSW	8	16,710,618 (GRCm38)	missense	probably benign	0.29
R0926:Csmd1	UTSW	8	16,033,576 (GRCm38)	splice site	probably null
R1005:Csmd1	UTSW	8	16,288,693 (GRCm38)	missense	probably damaging	0.99
R1073:Csmd1	UTSW	8	16,358,463 (GRCm38)	splice site	probably benign
R1185:Csmd1	UTSW	8	16,358,348 (GRCm38)	missense	probably damaging	0.96
R1185:Csmd1	UTSW	8	16,358,348 (GRCm38)	missense	probably damaging	0.96
R1185:Csmd1	UTSW	8	16,358,348 (GRCm38)	missense	probably damaging	0.96
R1256:Csmd1	UTSW	8	16,079,964 (GRCm38)	missense	probably damaging	1.00
R1294:Csmd1	UTSW	8	16,698,036 (GRCm38)	missense	probably damaging	0.99
R1375:Csmd1	UTSW	8	16,463,081 (GRCm38)	splice site	probably null
R1447:Csmd1	UTSW	8	15,925,306 (GRCm38)	nonsense	probably null
R1450:Csmd1	UTSW	8	15,945,180 (GRCm38)	critical splice acceptor site	probably null
R1470:Csmd1	UTSW	8	16,157,204 (GRCm38)	splice site	probably benign
R1580:Csmd1	UTSW	8	15,925,299 (GRCm38)	missense	probably damaging	1.00
R1591:Csmd1	UTSW	8	15,900,710 (GRCm38)	missense	probably damaging	0.99
R1658:Csmd1	UTSW	8	16,081,725 (GRCm38)	missense	possibly damaging	0.69
R1678:Csmd1	UTSW	8	15,918,252 (GRCm38)	missense	possibly damaging	0.58
R1717:Csmd1	UTSW	8	17,216,692 (GRCm38)	missense	possibly damaging	0.58
R1735:Csmd1	UTSW	8	15,932,610 (GRCm38)	missense	probably damaging	0.99
R1750:Csmd1	UTSW	8	15,917,303 (GRCm38)	missense	probably damaging	0.99
R1753:Csmd1	UTSW	8	16,157,120 (GRCm38)	nonsense	probably null
R1822:Csmd1	UTSW	8	16,223,326 (GRCm38)	missense	probably damaging	1.00
R1875:Csmd1	UTSW	8	15,929,101 (GRCm38)	missense	probably damaging	0.99
R1909:Csmd1	UTSW	8	15,906,116 (GRCm38)	missense	probably damaging	1.00
R1912:Csmd1	UTSW	8	16,233,998 (GRCm38)	critical splice donor site	probably null
R1993:Csmd1	UTSW	8	16,346,684 (GRCm38)	missense	probably damaging	0.99
R2067:Csmd1	UTSW	8	15,900,782 (GRCm38)	missense	probably benign
R2094:Csmd1	UTSW	8	16,079,978 (GRCm38)	missense	probably damaging	0.99
R2119:Csmd1	UTSW	8	17,216,733 (GRCm38)	missense	probably damaging	0.98
R2127:Csmd1	UTSW	8	15,917,392 (GRCm38)	missense	probably damaging	1.00
R2138:Csmd1	UTSW	8	15,929,088 (GRCm38)	missense	probably damaging	0.96
R2216:Csmd1	UTSW	8	17,027,339 (GRCm38)	critical splice acceptor site	probably null
R2220:Csmd1	UTSW	8	15,992,641 (GRCm38)	missense	possibly damaging	0.94
R2380:Csmd1	UTSW	8	16,190,087 (GRCm38)	missense	probably damaging	1.00
R2471:Csmd1	UTSW	8	16,211,762 (GRCm38)	missense	probably damaging	1.00
R2984:Csmd1	UTSW	8	15,953,782 (GRCm38)	missense	probably damaging	1.00
R3001:Csmd1	UTSW	8	16,196,170 (GRCm38)	missense	probably damaging	0.98
R3002:Csmd1	UTSW	8	16,196,170 (GRCm38)	missense	probably damaging	0.98
R3003:Csmd1	UTSW	8	16,196,170 (GRCm38)	missense	probably damaging	0.98
R3103:Csmd1	UTSW	8	15,917,405 (GRCm38)	missense	probably damaging	1.00
R3104:Csmd1	UTSW	8	17,027,231 (GRCm38)	missense	probably damaging	1.00
R3620:Csmd1	UTSW	8	15,992,684 (GRCm38)	missense	probably benign	0.29
R3621:Csmd1	UTSW	8	15,992,684 (GRCm38)	missense	probably benign	0.29
R3748:Csmd1	UTSW	8	15,906,071 (GRCm38)	missense	probably damaging	0.99
R3780:Csmd1	UTSW	8	16,201,986 (GRCm38)	missense	probably damaging	1.00
R3815:Csmd1	UTSW	8	16,002,522 (GRCm38)	missense	probably damaging	1.00
R3816:Csmd1	UTSW	8	16,002,522 (GRCm38)	missense	probably damaging	1.00
R3818:Csmd1	UTSW	8	16,002,522 (GRCm38)	missense	probably damaging	1.00
R3819:Csmd1	UTSW	8	16,002,522 (GRCm38)	missense	probably damaging	1.00
R3850:Csmd1	UTSW	8	16,079,922 (GRCm38)	missense	probably benign	0.00
R3945:Csmd1	UTSW	8	15,910,619 (GRCm38)	splice site	probably null
R3980:Csmd1	UTSW	8	15,906,056 (GRCm38)	nonsense	probably null
R4061:Csmd1	UTSW	8	15,945,158 (GRCm38)	missense	probably benign	0.00
R4086:Csmd1	UTSW	8	15,992,738 (GRCm38)	missense	probably damaging	0.99
R4087:Csmd1	UTSW	8	15,992,738 (GRCm38)	missense	probably damaging	0.99
R4089:Csmd1	UTSW	8	15,992,738 (GRCm38)	missense	probably damaging	0.99
R4183:Csmd1	UTSW	8	15,910,464 (GRCm38)	missense	probably damaging	0.99
R4226:Csmd1	UTSW	8	16,000,490 (GRCm38)	missense	probably damaging	0.99
R4454:Csmd1	UTSW	8	15,945,011 (GRCm38)	missense	probably damaging	0.99
R4533:Csmd1	UTSW	8	15,931,037 (GRCm38)	splice site	probably null
R4544:Csmd1	UTSW	8	16,710,636 (GRCm38)	missense	possibly damaging	0.93
R4547:Csmd1	UTSW	8	16,391,797 (GRCm38)	missense	possibly damaging	0.48
R4612:Csmd1	UTSW	8	15,921,908 (GRCm38)	splice site	probably null
R4620:Csmd1	UTSW	8	16,002,694 (GRCm38)	critical splice acceptor site	probably null
R4627:Csmd1	UTSW	8	16,697,917 (GRCm38)	missense	probably benign	0.00
R4633:Csmd1	UTSW	8	16,002,620 (GRCm38)	missense	probably damaging	0.99
R4646:Csmd1	UTSW	8	15,932,511 (GRCm38)	missense	possibly damaging	0.87
R4648:Csmd1	UTSW	8	15,998,788 (GRCm38)	nonsense	probably null
R4668:Csmd1	UTSW	8	16,023,891 (GRCm38)	missense	possibly damaging	0.50
R4709:Csmd1	UTSW	8	16,710,506 (GRCm38)	critical splice donor site	probably null
R4709:Csmd1	UTSW	8	16,023,891 (GRCm38)	missense	possibly damaging	0.96
R4741:Csmd1	UTSW	8	15,910,447 (GRCm38)	missense	probably damaging	0.99
R4774:Csmd1	UTSW	8	16,009,369 (GRCm38)	missense	probably benign	0.11
R4793:Csmd1	UTSW	8	16,088,263 (GRCm38)	missense	probably damaging	1.00
R4829:Csmd1	UTSW	8	16,127,296 (GRCm38)	missense	probably damaging	1.00
R4888:Csmd1	UTSW	8	15,895,674 (GRCm38)	utr 3 prime	probably benign
R4896:Csmd1	UTSW	8	16,009,439 (GRCm38)	missense	probably benign	0.00
R4932:Csmd1	UTSW	8	16,023,765 (GRCm38)	missense	probably damaging	0.99
R4944:Csmd1	UTSW	8	15,998,772 (GRCm38)	missense	probably damaging	1.00
R4953:Csmd1	UTSW	8	16,199,917 (GRCm38)	missense	probably damaging	0.99
R4996:Csmd1	UTSW	8	15,910,452 (GRCm38)	missense	probably damaging	0.97
R5028:Csmd1	UTSW	8	15,989,090 (GRCm38)	missense	probably damaging	1.00
R5146:Csmd1	UTSW	8	16,196,190 (GRCm38)	missense	probably damaging	1.00
R5272:Csmd1	UTSW	8	16,199,944 (GRCm38)	missense	probably damaging	0.99
R5327:Csmd1	UTSW	8	17,216,712 (GRCm38)	missense	possibly damaging	0.94
R5399:Csmd1	UTSW	8	16,710,597 (GRCm38)	missense	probably damaging	1.00
R5411:Csmd1	UTSW	8	15,910,471 (GRCm38)	missense	probably damaging	1.00
R5462:Csmd1	UTSW	8	15,961,486 (GRCm38)	missense	probably benign	0.12
R5463:Csmd1	UTSW	8	15,984,860 (GRCm38)	missense	probably benign	0.34
R5497:Csmd1	UTSW	8	16,085,181 (GRCm38)	missense	probably benign	0.20
R5536:Csmd1	UTSW	8	16,288,660 (GRCm38)	missense	probably damaging	0.99
R5711:Csmd1	UTSW	8	15,953,703 (GRCm38)	missense	probably damaging	1.00
R5730:Csmd1	UTSW	8	16,185,192 (GRCm38)	nonsense	probably null
R5788:Csmd1	UTSW	8	16,201,966 (GRCm38)	missense	probably damaging	1.00
R5941:Csmd1	UTSW	8	15,932,471 (GRCm38)	missense	probably damaging	0.99
R5960:Csmd1	UTSW	8	16,071,416 (GRCm38)	missense	possibly damaging	0.68
R5961:Csmd1	UTSW	8	16,070,352 (GRCm38)	missense	probably damaging	0.99
R5969:Csmd1	UTSW	8	16,071,353 (GRCm38)	missense	probably benign	0.00
R5998:Csmd1	UTSW	8	15,910,443 (GRCm38)	missense	probably damaging	1.00
R6062:Csmd1	UTSW	8	16,092,305 (GRCm38)	missense	possibly damaging	0.68
R6109:Csmd1	UTSW	8	16,199,860 (GRCm38)	missense	possibly damaging	0.93
R6116:Csmd1	UTSW	8	16,211,850 (GRCm38)	missense	probably damaging	1.00
R6143:Csmd1	UTSW	8	16,088,301 (GRCm38)	missense	probably damaging	1.00
R6155:Csmd1	UTSW	8	15,903,231 (GRCm38)	missense	probably benign	0.01
R6197:Csmd1	UTSW	8	15,926,611 (GRCm38)	missense	probably benign	0.32
R6247:Csmd1	UTSW	8	16,196,235 (GRCm38)	missense	possibly damaging	0.91
R6304:Csmd1	UTSW	8	16,058,674 (GRCm38)	missense	probably damaging	1.00
R6317:Csmd1	UTSW	8	16,710,642 (GRCm38)	missense	possibly damaging	0.89
R6318:Csmd1	UTSW	8	15,903,212 (GRCm38)	missense	probably damaging	1.00
R6338:Csmd1	UTSW	8	15,932,492 (GRCm38)	missense	possibly damaging	0.75
R6369:Csmd1	UTSW	8	17,535,004 (GRCm38)	start gained	probably benign
R6447:Csmd1	UTSW	8	15,910,527 (GRCm38)	missense	probably damaging	1.00
R6454:Csmd1	UTSW	8	15,921,150 (GRCm38)	missense	probably damaging	0.99
R6494:Csmd1	UTSW	8	16,211,695 (GRCm38)	splice site	probably null
R6614:Csmd1	UTSW	8	17,216,787 (GRCm38)	missense	probably damaging	1.00
R6736:Csmd1	UTSW	8	16,002,626 (GRCm38)	missense	probably damaging	0.99
R6769:Csmd1	UTSW	8	16,071,394 (GRCm38)	missense	possibly damaging	0.80
R6771:Csmd1	UTSW	8	16,071,394 (GRCm38)	missense	possibly damaging	0.80
R6804:Csmd1	UTSW	8	16,037,246 (GRCm38)	missense	probably damaging	1.00
R6818:Csmd1	UTSW	8	16,185,327 (GRCm38)	missense	probably damaging	1.00
R6863:Csmd1	UTSW	8	17,534,913 (GRCm38)	missense	possibly damaging	0.85
R6930:Csmd1	UTSW	8	16,092,395 (GRCm38)	missense	probably damaging	0.97
R6969:Csmd1	UTSW	8	17,216,789 (GRCm38)	missense	possibly damaging	0.94
R7112:Csmd1	UTSW	8	16,101,128 (GRCm38)	missense	probably damaging	1.00
R7124:Csmd1	UTSW	8	15,903,202 (GRCm38)	missense	probably damaging	1.00
R7167:Csmd1	UTSW	8	15,926,524 (GRCm38)	missense	probably benign
R7243:Csmd1	UTSW	8	15,915,357 (GRCm38)	missense	probably damaging	1.00
R7260:Csmd1	UTSW	8	16,000,574 (GRCm38)	missense	probably damaging	1.00
R7271:Csmd1	UTSW	8	17,027,279 (GRCm38)	missense	probably damaging	0.99
R7324:Csmd1	UTSW	8	16,058,707 (GRCm38)	missense	probably damaging	1.00
R7325:Csmd1	UTSW	8	16,058,707 (GRCm38)	missense	probably damaging	1.00
R7327:Csmd1	UTSW	8	16,058,707 (GRCm38)	missense	probably damaging	1.00
R7373:Csmd1	UTSW	8	15,992,713 (GRCm38)	missense	probably damaging	1.00
R7406:Csmd1	UTSW	8	16,288,693 (GRCm38)	missense	probably damaging	0.99
R7427:Csmd1	UTSW	8	16,023,850 (GRCm38)	missense	possibly damaging	0.91
R7428:Csmd1	UTSW	8	16,023,850 (GRCm38)	missense	possibly damaging	0.91
R7445:Csmd1	UTSW	8	16,158,254 (GRCm38)	missense	possibly damaging	0.61
R7458:Csmd1	UTSW	8	15,953,738 (GRCm38)	missense	probably damaging	1.00
R7476:Csmd1	UTSW	8	15,895,731 (GRCm38)	missense	probably damaging	1.00
R7544:Csmd1	UTSW	8	16,092,296 (GRCm38)	missense	probably damaging	1.00
R7583:Csmd1	UTSW	8	15,998,833 (GRCm38)	missense	probably damaging	0.96
R7603:Csmd1	UTSW	8	16,288,682 (GRCm38)	missense	probably damaging	1.00
R7607:Csmd1	UTSW	8	15,918,331 (GRCm38)	missense	possibly damaging	0.94
R7642:Csmd1	UTSW	8	16,085,178 (GRCm38)	missense	probably damaging	0.99
R7669:Csmd1	UTSW	8	15,917,273 (GRCm38)	missense	probably damaging	1.00
R7720:Csmd1	UTSW	8	15,931,108 (GRCm38)	missense	probably damaging	1.00
R7728:Csmd1	UTSW	8	16,231,271 (GRCm38)	missense	probably damaging	1.00
R7738:Csmd1	UTSW	8	16,100,990 (GRCm38)	missense	probably damaging	1.00
R7745:Csmd1	UTSW	8	15,932,461 (GRCm38)	critical splice donor site	probably null
R7879:Csmd1	UTSW	8	16,391,806 (GRCm38)	missense	probably benign	0.28
R7884:Csmd1	UTSW	8	15,961,418 (GRCm38)	missense	probably damaging	1.00
R7897:Csmd1	UTSW	8	17,534,919 (GRCm38)	missense	possibly damaging	0.96
R8111:Csmd1	UTSW	8	15,917,306 (GRCm38)	missense	probably benign
R8119:Csmd1	UTSW	8	17,027,294 (GRCm38)	missense	probably damaging	0.99
R8134:Csmd1	UTSW	8	15,932,550 (GRCm38)	missense	probably damaging	0.99
R8187:Csmd1	UTSW	8	16,127,174 (GRCm38)	missense	probably damaging	0.99
R8196:Csmd1	UTSW	8	16,009,468 (GRCm38)	missense	probably benign	0.18
R8231:Csmd1	UTSW	8	16,697,923 (GRCm38)	missense	possibly damaging	0.82
R8242:Csmd1	UTSW	8	16,710,654 (GRCm38)	missense	probably benign	0.42
R8274:Csmd1	UTSW	8	15,910,453 (GRCm38)	missense	possibly damaging	0.93
R8286:Csmd1	UTSW	8	15,989,188 (GRCm38)	missense	probably benign	0.18
R8289:Csmd1	UTSW	8	16,058,702 (GRCm38)	missense	probably damaging	0.99
R8314:Csmd1	UTSW	8	16,158,244 (GRCm38)	missense	probably benign
R8323:Csmd1	UTSW	8	17,216,735 (GRCm38)	nonsense	probably null
R8387:Csmd1	UTSW	8	16,000,484 (GRCm38)	missense	possibly damaging	0.94
R8413:Csmd1	UTSW	8	15,900,676 (GRCm38)	missense	probably damaging	0.98
R8672:Csmd1	UTSW	8	15,926,598 (GRCm38)	missense	probably benign	0.01
R8765:Csmd1	UTSW	8	16,710,611 (GRCm38)	nonsense	probably null
R8789:Csmd1	UTSW	8	17,216,706 (GRCm38)	missense	probably damaging	0.99
R8828:Csmd1	UTSW	8	15,998,794 (GRCm38)	missense	probably benign	0.00
R8858:Csmd1	UTSW	8	16,070,304 (GRCm38)	missense	probably benign	0.10
R8878:Csmd1	UTSW	8	15,910,528 (GRCm38)	missense	probably damaging	1.00
R8911:Csmd1	UTSW	8	16,698,003 (GRCm38)	missense	probably damaging	0.99
R8966:Csmd1	UTSW	8	16,200,045 (GRCm38)	missense	probably damaging	1.00
R8978:Csmd1	UTSW	8	15,921,056 (GRCm38)	missense	probably benign	0.37
R8996:Csmd1	UTSW	8	15,921,105 (GRCm38)	missense	possibly damaging	0.54
R9045:Csmd1	UTSW	8	16,234,074 (GRCm38)	missense	probably damaging	0.99
R9084:Csmd1	UTSW	8	16,088,311 (GRCm38)	missense	probably benign
R9124:Csmd1	UTSW	8	15,984,806 (GRCm38)	missense	probably damaging	0.99
R9127:Csmd1	UTSW	8	16,223,272 (GRCm38)	missense	probably benign	0.31
R9146:Csmd1	UTSW	8	15,998,832 (GRCm38)	missense	probably benign	0.00
R9198:Csmd1	UTSW	8	15,912,430 (GRCm38)	missense	probably damaging	1.00
R9285:Csmd1	UTSW	8	15,906,088 (GRCm38)	missense	probably damaging	1.00
R9303:Csmd1	UTSW	8	15,961,532 (GRCm38)	missense	probably benign	0.31
R9305:Csmd1	UTSW	8	15,961,532 (GRCm38)	missense	probably benign	0.31
R9326:Csmd1	UTSW	8	15,999,803 (GRCm38)	missense	probably benign	0.21
R9356:Csmd1	UTSW	8	16,202,055 (GRCm38)	missense	probably damaging	1.00
R9385:Csmd1	UTSW	8	15,984,756 (GRCm38)	missense	probably benign	0.19
R9444:Csmd1	UTSW	8	16,158,236 (GRCm38)	missense	probably benign	0.30
R9476:Csmd1	UTSW	8	15,931,215 (GRCm38)	critical splice acceptor site	probably null
R9506:Csmd1	UTSW	8	16,200,009 (GRCm38)	missense	probably damaging	1.00
R9614:Csmd1	UTSW	8	16,158,225 (GRCm38)	missense	probably benign	0.00
R9668:Csmd1	UTSW	8	16,211,758 (GRCm38)	missense	probably benign	0.00
X0011:Csmd1	UTSW	8	16,196,263 (GRCm38)	missense	probably damaging	1.00
X0021:Csmd1	UTSW	8	16,185,256 (GRCm38)	missense	probably damaging	1.00
X0024:Csmd1	UTSW	8	16,037,218 (GRCm38)	missense	probably damaging	0.99
X0028:Csmd1	UTSW	8	15,915,333 (GRCm38)	missense	possibly damaging	0.79
Z1088:Csmd1	UTSW	8	16,189,978 (GRCm38)	missense	possibly damaging	0.50
Z1088:Csmd1	UTSW	8	16,092,258 (GRCm38)	missense	probably damaging	1.00
Z1088:Csmd1	UTSW	8	15,921,875 (GRCm38)	missense	possibly damaging	0.91
Z1088:Csmd1	UTSW	8	16,346,617 (GRCm38)	missense	probably damaging	0.99
Z1088:Csmd1	UTSW	8	16,200,058 (GRCm38)	missense	probably damaging	0.97
Z1176:Csmd1	UTSW	8	16,037,198 (GRCm38)	missense	probably damaging	1.00
Z1176:Csmd1	UTSW	8	15,998,814 (GRCm38)	missense	probably damaging	1.00
Z1177:Csmd1	UTSW	8	16,200,019 (GRCm38)	missense	probably damaging	1.00
Z1177:Csmd1	UTSW	8	15,984,708 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCAACTTTCAAATGTGCTGTG -3'
(R):5'- CAGAAAGCCTTTCAGTCTTCTGTC -3'

Sequencing Primer
(F):5'- CAAATGTGCTGTGCTTTAAGAGTAC -3'
(R):5'- TGCCCATGCAGGTGTGACTC -3'

Posted On

2019-10-17