Mutagenetix > Incidental Mutation

Incidental Mutation 'R4820:Fras1'

370118

Institutional Source

Beutler Lab

Gene Symbol

Fras1

Ensembl Gene

ENSMUSG00000034687

Gene Name

Fraser extracellular matrix complex subunit 1

Synonyms

bl, E130113P14Rik

MMRRC Submission

042436-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4820 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

96521814-96932587 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 96876512 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 2415 (I2415T)

Ref Sequence

ENSEMBL: ENSMUSP00000043250 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000036019]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000036019
AA Change: I2415T

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000043250
Gene: ENSMUSG00000034687
AA Change: I2415T

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
VWC	27	86	9.23e-9	SMART
VWC	94	151	9.37e-10	SMART
VWC	158	215	8.61e-9	SMART
VWC	220	277	7.1e-10	SMART
VWC	284	341	7.8e-7	SMART
VWC	365	415	1.93e-1	SMART
FU	408	459	3.33e-1	SMART
FU	461	504	9.12e-8	SMART
EGF_like	466	495	6.67e1	SMART
FU	506	552	6.01e-8	SMART
FU	554	598	2.21e-6	SMART
FU	601	646	1.28e-11	SMART
FU	648	704	4.19e-7	SMART
FU	707	752	9.12e-8	SMART
FU	754	799	1.11e-6	SMART
EGF_like	759	790	7.23e1	SMART
FU	802	851	5.44e-6	SMART
EGF_like	807	842	4.55e1	SMART
FU	853	899	7.4e-8	SMART
FU	902	947	4.78e-2	SMART
FU	951	996	4.52e-12	SMART
EGF_like	956	987	2.75e1	SMART
FU	998	1041	1.38e-7	SMART
FU	1045	1088	9.7e-3	SMART
EGF_like	1057	1096	3.16e1	SMART
Pfam:Cadherin_3	1098	1198	5.2e-12	PFAM
Pfam:Cadherin_3	1167	1309	6.5e-27	PFAM
Pfam:Cadherin_3	1278	1442	7e-24	PFAM
Pfam:Cadherin_3	1411	1560	1.3e-23	PFAM
Pfam:Cadherin_3	1561	1693	6.4e-15	PFAM
Pfam:Cadherin_3	1695	1814	1.1e-10	PFAM
Pfam:Cadherin_3	1780	1940	1.6e-18	PFAM
Pfam:Cadherin_3	1906	2061	2.8e-22	PFAM
Pfam:Cadherin_3	2063	2181	3.3e-18	PFAM
Pfam:Cadherin_3	2172	2295	1.4e-26	PFAM
Pfam:Cadherin_3	2296	2408	2.3e-31	PFAM
Pfam:Cadherin_3	2413	2540	7.9e-23	PFAM
Calx_beta	2544	2648	1.23e-10	SMART
Calx_beta	2661	2772	3.3e-11	SMART
Calx_beta	2787	2892	1.21e-9	SMART
Calx_beta	2907	3009	4.45e-3	SMART
Calx_beta	3027	3131	1.5e-14	SMART
Blast:Calx_beta	3162	3187	1e-5	BLAST
transmembrane domain	3902	3924	N/A	INTRINSIC
low complexity region	3927	3935	N/A	INTRINSIC

Meta Mutation Damage Score

0.0823

Coding Region Coverage

1x: 99.0%
3x: 98.3%
10x: 96.5%
20x: 92.9%

Validation Efficiency

96% (104/108)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
PHENOTYPE: Mice homozygous for mutations at this locus display a significant amount of embryonic lethality due to hemorrhaging of embryonic blisters. Survival is variable on genetic backgrounds. Kidney development is severely affected and syndactyly is common. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 95 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930488N24Rik	T	C	17: 14,326,481 (GRCm39)		noncoding transcript	Het
5730455P16Rik	A	T	11: 80,266,346 (GRCm39)	S132T	possibly damaging	Het
Aadacl3	T	A	4: 144,184,527 (GRCm39)	H77L	probably damaging	Het
Actr5	T	A	2: 158,467,426 (GRCm39)	V122D	probably damaging	Het
Adamts7	A	G	9: 90,071,739 (GRCm39)	D678G	possibly damaging	Het
Alpk1	T	A	3: 127,464,708 (GRCm39)	D1190V	probably benign	Het
Apbb1ip	A	T	2: 22,765,265 (GRCm39)	N649Y	unknown	Het
Atp6v0a1	A	G	11: 100,933,776 (GRCm39)	I522V	probably benign	Het
Brd10	T	C	19: 29,695,809 (GRCm39)	N1228S	possibly damaging	Het
Cars1	T	C	7: 143,124,301 (GRCm39)	D375G	probably damaging	Het
Catspere1	A	T	1: 177,687,441 (GRCm39)		noncoding transcript	Het
Ccdc87	A	G	19: 4,890,579 (GRCm39)	D357G	probably damaging	Het
Cd101	A	T	3: 100,929,471 (GRCm39)	S8T	probably benign	Het
Cfap65	C	T	1: 74,966,791 (GRCm39)	A299T	probably benign	Het
Cic	T	C	7: 24,971,157 (GRCm39)	V296A	possibly damaging	Het
Col7a1	T	A	9: 108,797,675 (GRCm39)	S1686T	possibly damaging	Het
Ctbp2	A	C	7: 132,615,423 (GRCm39)	L504R	probably damaging	Het
Cttnbp2nl	T	C	3: 104,918,640 (GRCm39)	K67E	probably benign	Het
Cyp2c50	C	T	19: 40,102,024 (GRCm39)	P480S	probably damaging	Het
Dcdc5	A	C	2: 106,166,420 (GRCm39)		noncoding transcript	Het
Defb2	G	T	8: 22,333,317 (GRCm39)	E31*	probably null	Het
Dhrs1	T	A	14: 55,977,083 (GRCm39)	N244I	possibly damaging	Het
Dop1b	A	G	16: 93,589,978 (GRCm39)	I134V	probably benign	Het
Eif1ad11	A	T	12: 87,994,158 (GRCm39)	I129F	unknown	Het
Etl4	A	G	2: 20,811,496 (GRCm39)	D1193G	possibly damaging	Het
Ezh1	A	C	11: 101,094,594 (GRCm39)	S399R	probably damaging	Het
Fam161a	T	C	11: 22,970,076 (GRCm39)	S26P	probably damaging	Het
Fcgbp	C	A	7: 27,813,383 (GRCm39)	S2306Y	probably damaging	Het
Gas2l3	A	G	10: 89,252,907 (GRCm39)	L246P	probably damaging	Het
Gdf15	C	T	8: 71,082,246 (GRCm39)	V287M	probably damaging	Het
Gm7742	T	C	17: 21,420,235 (GRCm39)		noncoding transcript	Het
Grin2d	T	C	7: 45,507,363 (GRCm39)	D446G	probably damaging	Het
Hemk1	A	G	9: 107,205,385 (GRCm39)	F107L	probably benign	Het
Hmgcr	C	T	13: 96,796,700 (GRCm39)	G197S	probably damaging	Het
Ift52	G	A	2: 162,873,108 (GRCm39)	G207D	probably benign	Het
Il17re	A	G	6: 113,442,816 (GRCm39)	T275A	probably benign	Het
Iqcf3	T	C	9: 106,430,788 (GRCm39)		probably benign	Het
Kcna1	A	G	6: 126,619,099 (GRCm39)	I407T	probably damaging	Het
Kcnrg	T	A	14: 61,845,386 (GRCm39)	M142K	probably benign	Het
Lhx9	C	A	1: 138,766,105 (GRCm39)	V237L	probably benign	Het
Lipo3	A	C	19: 33,560,497 (GRCm39)	I56S	probably damaging	Het
Loxhd1	C	G	18: 77,472,663 (GRCm39)	P1060R	probably damaging	Het
Map2k4	A	C	11: 65,587,201 (GRCm39)		probably benign	Het
Methig1	A	G	15: 100,251,416 (GRCm39)	K109R	possibly damaging	Het
Mmrn1	G	A	6: 60,950,027 (GRCm39)	V326I	probably benign	Het
Myo15a	G	A	11: 60,367,741 (GRCm39)	R167H	probably damaging	Het
Ncoa7	G	A	10: 30,524,472 (GRCm39)	T142M	probably damaging	Het
Nfkb2	C	A	19: 46,296,493 (GRCm39)	Q254K	probably damaging	Het
Nherf1	A	G	11: 115,070,918 (GRCm39)	E290G	probably benign	Het
Nol6	G	T	4: 41,121,508 (GRCm39)	P278Q	probably damaging	Het
Nptxr	T	A	15: 79,677,027 (GRCm39)	D285V	probably damaging	Het
Oosp3	T	C	19: 11,688,997 (GRCm39)	W82R	probably damaging	Het
Or6b3	A	T	1: 92,438,812 (GRCm39)	*313K	probably null	Het
Or6n1	A	G	1: 173,916,742 (GRCm39)	I45M	possibly damaging	Het
Pa2g4	G	T	10: 128,395,199 (GRCm39)	T322K	probably damaging	Het
Parp16	C	A	9: 65,145,175 (GRCm39)	F291L	probably damaging	Het
Pdzd9	A	T	7: 120,267,619 (GRCm39)	D65E	probably damaging	Het
Pgap3	A	G	11: 98,281,300 (GRCm39)	W238R	probably damaging	Het
Pgf	G	A	12: 85,218,538 (GRCm39)	H67Y	probably benign	Het
Pik3cb	T	C	9: 98,955,679 (GRCm39)	T413A	probably benign	Het
Plcxd2	A	T	16: 45,800,700 (GRCm39)	C175S	probably benign	Het
Pou2f1	A	T	1: 165,719,517 (GRCm39)		probably benign	Het
Ppfia1	T	G	7: 144,052,106 (GRCm39)	N846T	probably benign	Het
Ppid	T	A	3: 79,502,504 (GRCm39)		probably null	Het
Prkcq	G	A	2: 11,231,797 (GRCm39)		probably null	Het
Ptgds	T	C	2: 25,359,058 (GRCm39)	K66E	probably benign	Het
Ptpmt1	A	G	2: 90,748,283 (GRCm39)		noncoding transcript	Het
Rab3il1	G	A	19: 10,004,034 (GRCm39)	G51D	probably benign	Het
Rdx	T	C	9: 51,974,891 (GRCm39)	V9A	probably damaging	Het
Rpl7l1	T	C	17: 47,089,014 (GRCm39)	N239S	probably benign	Het
Rrbp1	C	A	2: 143,806,685 (GRCm39)	A978S	possibly damaging	Het
Rsf1	GCGGCGGCG	GCGGCGGCGCCGGCGGCG	7: 97,229,126 (GRCm39)		probably benign	Het
Scn3a	A	T	2: 65,291,622 (GRCm39)	I1708N	probably damaging	Het
Serinc1	A	G	10: 57,401,466 (GRCm39)	I109T	possibly damaging	Het
Shroom1	G	A	11: 53,355,966 (GRCm39)	V339I	probably benign	Het
Slc30a8	T	A	15: 52,169,880 (GRCm39)	C36S	probably benign	Het
Slco1b2	A	G	6: 141,631,158 (GRCm39)	I597M	probably benign	Het
Snx27	A	G	3: 94,427,518 (GRCm39)	F228S	probably damaging	Het
Spata31f1a	T	A	4: 42,851,815 (GRCm39)	I114F	probably damaging	Het
Speer4e2	G	T	5: 15,026,225 (GRCm39)	T144K	probably benign	Het
Stim1	T	A	7: 102,064,571 (GRCm39)	F214I	probably damaging	Het
Svep1	T	C	4: 58,082,664 (GRCm39)	T1987A	probably benign	Het
Tamm41	A	G	6: 115,002,378 (GRCm39)	I18T	possibly damaging	Het
Tmem150b	T	A	7: 4,726,871 (GRCm39)	D79V	probably damaging	Het
Tmem167	T	A	13: 90,252,548 (GRCm39)	I68N	probably benign	Het
Traf3	A	G	12: 111,227,204 (GRCm39)	E339G	possibly damaging	Het
Tspan12	G	A	6: 21,795,660 (GRCm39)	P177S	probably damaging	Het
Ttn	A	G	2: 76,783,562 (GRCm39)	I810T	probably benign	Het
Ulk1	T	C	5: 110,939,996 (GRCm39)	T407A	probably benign	Het
Uroc1	G	A	6: 90,334,600 (GRCm39)		probably null	Het
Vmn2r-ps69	T	C	7: 84,959,584 (GRCm39)		noncoding transcript	Het
Wdr59	T	C	8: 112,207,446 (GRCm39)	N476S	probably benign	Het
Zfp472	A	G	17: 33,196,416 (GRCm39)	M164V	probably benign	Het
Zfp608	T	C	18: 55,120,756 (GRCm39)	N277S	probably benign	Het
Zfp831	T	C	2: 174,547,097 (GRCm39)	C1427R	possibly damaging	Het

Other mutations in Fras1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00332:Fras1	APN	5	96,887,217 (GRCm39)	missense	possibly damaging	0.55
IGL00507:Fras1	APN	5	96,926,048 (GRCm39)	missense	probably damaging	1.00
IGL00672:Fras1	APN	5	96,907,309 (GRCm39)	splice site	probably benign
IGL00772:Fras1	APN	5	96,783,971 (GRCm39)	missense	probably benign	0.42
IGL00844:Fras1	APN	5	96,682,712 (GRCm39)	splice site	probably benign
IGL00913:Fras1	APN	5	96,842,935 (GRCm39)	missense	probably damaging	0.99
IGL00959:Fras1	APN	5	96,929,140 (GRCm39)	missense	probably damaging	0.96
IGL00966:Fras1	APN	5	96,703,080 (GRCm39)	missense	probably benign	0.00
IGL01296:Fras1	APN	5	96,821,557 (GRCm39)	missense	probably null	0.58
IGL01307:Fras1	APN	5	96,929,551 (GRCm39)	missense	probably benign
IGL01481:Fras1	APN	5	96,805,100 (GRCm39)	missense	probably damaging	1.00
IGL01525:Fras1	APN	5	96,887,195 (GRCm39)	missense	probably damaging	0.99
IGL01599:Fras1	APN	5	96,857,750 (GRCm39)	missense	possibly damaging	0.94
IGL01646:Fras1	APN	5	96,906,007 (GRCm39)	missense	probably benign	0.29
IGL01795:Fras1	APN	5	96,925,904 (GRCm39)	missense	probably damaging	1.00
IGL01867:Fras1	APN	5	96,735,990 (GRCm39)	missense	probably benign
IGL01869:Fras1	APN	5	96,856,642 (GRCm39)	splice site	probably benign
IGL01923:Fras1	APN	5	96,883,139 (GRCm39)	missense	probably damaging	1.00
IGL01982:Fras1	APN	5	96,887,107 (GRCm39)	missense	possibly damaging	0.46
IGL02109:Fras1	APN	5	96,848,382 (GRCm39)	missense	probably benign
IGL02132:Fras1	APN	5	96,929,496 (GRCm39)	nonsense	probably null
IGL02171:Fras1	APN	5	96,883,040 (GRCm39)	missense	probably benign	0.15
IGL02213:Fras1	APN	5	96,793,730 (GRCm39)	nonsense	probably null
IGL02277:Fras1	APN	5	96,735,977 (GRCm39)	missense	probably benign	0.00
IGL02507:Fras1	APN	5	96,805,267 (GRCm39)	missense	possibly damaging	0.95
IGL02589:Fras1	APN	5	96,917,372 (GRCm39)	missense	probably damaging	1.00
IGL02671:Fras1	APN	5	96,876,475 (GRCm39)	missense	possibly damaging	0.91
IGL02677:Fras1	APN	5	96,692,883 (GRCm39)	missense	probably damaging	1.00
IGL02691:Fras1	APN	5	96,892,564 (GRCm39)	missense	possibly damaging	0.68
IGL02741:Fras1	APN	5	96,839,230 (GRCm39)	missense	probably benign	0.35
IGL02836:Fras1	APN	5	96,682,725 (GRCm39)	missense	possibly damaging	0.67
IGL02850:Fras1	APN	5	96,926,034 (GRCm39)	missense	probably damaging	1.00
IGL02998:Fras1	APN	5	96,850,040 (GRCm39)	missense	possibly damaging	0.82
IGL03040:Fras1	APN	5	96,857,960 (GRCm39)	missense	probably benign
IGL03078:Fras1	APN	5	96,783,994 (GRCm39)	missense	probably damaging	1.00
IGL03096:Fras1	APN	5	96,912,760 (GRCm39)	missense	probably damaging	1.00
IGL03102:Fras1	APN	5	96,874,394 (GRCm39)	missense	probably benign	0.11
IGL03183:Fras1	APN	5	96,881,640 (GRCm39)	splice site	probably benign
IGL03189:Fras1	APN	5	96,890,930 (GRCm39)	missense	probably benign	0.00
IGL03193:Fras1	APN	5	96,925,965 (GRCm39)	missense	probably damaging	0.99
IGL03292:Fras1	APN	5	96,855,350 (GRCm39)	missense	probably damaging	1.00
IGL03328:Fras1	APN	5	96,929,619 (GRCm39)	missense	probably damaging	0.96
IGL03335:Fras1	APN	5	96,881,803 (GRCm39)	splice site	probably benign
IGL03394:Fras1	APN	5	96,815,336 (GRCm39)	missense	probably damaging	0.98
IGL03404:Fras1	APN	5	96,876,440 (GRCm39)	missense	probably damaging	0.99
baby_ruth	UTSW	5	96,856,617 (GRCm39)	missense	probably benign	0.01
BB002:Fras1	UTSW	5	96,929,443 (GRCm39)	missense	probably damaging	0.96
BB012:Fras1	UTSW	5	96,929,443 (GRCm39)	missense	probably damaging	0.96
G1patch:Fras1	UTSW	5	96,929,199 (GRCm39)	missense	possibly damaging	0.91
I0000:Fras1	UTSW	5	96,888,688 (GRCm39)	missense	probably damaging	0.99
PIT4581001:Fras1	UTSW	5	96,703,160 (GRCm39)	missense	probably benign	0.01
R0028:Fras1	UTSW	5	96,825,175 (GRCm39)	missense	probably benign	0.07
R0049:Fras1	UTSW	5	96,924,481 (GRCm39)	missense	probably benign	0.07
R0049:Fras1	UTSW	5	96,924,481 (GRCm39)	missense	probably benign	0.07
R0099:Fras1	UTSW	5	96,762,776 (GRCm39)	critical splice donor site	probably null
R0109:Fras1	UTSW	5	96,857,936 (GRCm39)	missense	probably benign	0.01
R0158:Fras1	UTSW	5	96,924,493 (GRCm39)	missense	possibly damaging	0.83
R0268:Fras1	UTSW	5	96,884,868 (GRCm39)	missense	probably damaging	0.99
R0305:Fras1	UTSW	5	96,744,747 (GRCm39)	missense	probably benign
R0352:Fras1	UTSW	5	96,874,399 (GRCm39)	missense	probably damaging	0.97
R0359:Fras1	UTSW	5	96,910,449 (GRCm39)	missense	probably damaging	0.98
R0371:Fras1	UTSW	5	96,703,190 (GRCm39)	missense	possibly damaging	0.90
R0379:Fras1	UTSW	5	96,903,368 (GRCm39)	nonsense	probably null
R0395:Fras1	UTSW	5	96,917,512 (GRCm39)	missense	possibly damaging	0.50
R0417:Fras1	UTSW	5	96,839,231 (GRCm39)	missense	probably benign	0.18
R0454:Fras1	UTSW	5	96,910,524 (GRCm39)	missense	probably damaging	0.96
R0456:Fras1	UTSW	5	96,862,202 (GRCm39)	splice site	probably null
R0456:Fras1	UTSW	5	96,702,647 (GRCm39)	missense	probably damaging	1.00
R0464:Fras1	UTSW	5	96,784,662 (GRCm39)	missense	probably damaging	0.98
R0613:Fras1	UTSW	5	96,848,347 (GRCm39)	splice site	probably benign
R0652:Fras1	UTSW	5	96,929,199 (GRCm39)	missense	possibly damaging	0.91
R0675:Fras1	UTSW	5	96,815,246 (GRCm39)	splice site	probably benign
R0765:Fras1	UTSW	5	96,700,655 (GRCm39)	missense	probably benign	0.00
R0783:Fras1	UTSW	5	96,916,289 (GRCm39)	missense	probably damaging	1.00
R0811:Fras1	UTSW	5	96,900,857 (GRCm39)	missense	probably benign	0.35
R0812:Fras1	UTSW	5	96,900,857 (GRCm39)	missense	probably benign	0.35
R0943:Fras1	UTSW	5	96,874,402 (GRCm39)	missense	probably benign	0.00
R1037:Fras1	UTSW	5	96,862,322 (GRCm39)	missense	probably damaging	0.97
R1104:Fras1	UTSW	5	96,856,530 (GRCm39)	missense	probably benign	0.00
R1108:Fras1	UTSW	5	96,790,488 (GRCm39)	missense	probably damaging	0.99
R1332:Fras1	UTSW	5	96,855,167 (GRCm39)	missense	probably benign	0.00
R1336:Fras1	UTSW	5	96,855,167 (GRCm39)	missense	probably benign	0.00
R1458:Fras1	UTSW	5	96,748,592 (GRCm39)	missense	probably benign	0.00
R1495:Fras1	UTSW	5	96,676,445 (GRCm39)	missense	possibly damaging	0.49
R1499:Fras1	UTSW	5	96,891,046 (GRCm39)	missense	probably benign	0.31
R1528:Fras1	UTSW	5	96,784,678 (GRCm39)	missense	probably damaging	0.99
R1532:Fras1	UTSW	5	96,861,855 (GRCm39)	missense	probably damaging	1.00
R1556:Fras1	UTSW	5	96,890,921 (GRCm39)	missense	possibly damaging	0.88
R1625:Fras1	UTSW	5	96,857,837 (GRCm39)	missense	possibly damaging	0.94
R1625:Fras1	UTSW	5	96,861,849 (GRCm39)	missense	probably damaging	1.00
R1645:Fras1	UTSW	5	96,848,445 (GRCm39)	missense	possibly damaging	0.90
R1647:Fras1	UTSW	5	96,874,472 (GRCm39)	critical splice donor site	probably null
R1648:Fras1	UTSW	5	96,874,472 (GRCm39)	critical splice donor site	probably null
R1661:Fras1	UTSW	5	96,746,768 (GRCm39)	missense	probably damaging	1.00
R1665:Fras1	UTSW	5	96,746,768 (GRCm39)	missense	probably damaging	1.00
R1682:Fras1	UTSW	5	96,793,732 (GRCm39)	missense	probably benign	0.00
R1701:Fras1	UTSW	5	96,748,643 (GRCm39)	missense	probably benign	0.00
R1716:Fras1	UTSW	5	96,700,584 (GRCm39)	missense	probably benign	0.10
R1718:Fras1	UTSW	5	96,702,748 (GRCm39)	splice site	probably null
R1800:Fras1	UTSW	5	96,857,741 (GRCm39)	missense	probably benign
R1806:Fras1	UTSW	5	96,912,835 (GRCm39)	missense	possibly damaging	0.88
R1806:Fras1	UTSW	5	96,861,829 (GRCm39)	splice site	probably benign
R1822:Fras1	UTSW	5	96,918,547 (GRCm39)	missense	probably damaging	1.00
R1823:Fras1	UTSW	5	96,918,547 (GRCm39)	missense	probably damaging	1.00
R1824:Fras1	UTSW	5	96,918,547 (GRCm39)	missense	probably damaging	1.00
R1847:Fras1	UTSW	5	96,897,282 (GRCm39)	splice site	probably null
R1929:Fras1	UTSW	5	96,815,296 (GRCm39)	missense	probably benign	0.24
R1951:Fras1	UTSW	5	96,860,242 (GRCm39)	missense	probably benign	0.38
R2093:Fras1	UTSW	5	96,929,062 (GRCm39)	missense	probably damaging	1.00
R2283:Fras1	UTSW	5	96,802,164 (GRCm39)	missense	probably benign	0.10
R2884:Fras1	UTSW	5	96,848,127 (GRCm39)	missense	probably benign	0.07
R2913:Fras1	UTSW	5	96,881,774 (GRCm39)	missense	probably benign
R2914:Fras1	UTSW	5	96,881,774 (GRCm39)	missense	probably benign
R3054:Fras1	UTSW	5	96,912,802 (GRCm39)	missense	probably damaging	0.99
R3117:Fras1	UTSW	5	96,919,571 (GRCm39)	missense	probably damaging	1.00
R3118:Fras1	UTSW	5	96,919,571 (GRCm39)	missense	probably damaging	1.00
R3691:Fras1	UTSW	5	96,929,371 (GRCm39)	missense	probably benign	0.02
R3714:Fras1	UTSW	5	96,793,829 (GRCm39)	critical splice donor site	probably null
R3715:Fras1	UTSW	5	96,793,829 (GRCm39)	critical splice donor site	probably null
R3801:Fras1	UTSW	5	96,881,791 (GRCm39)	missense	probably benign	0.26
R3961:Fras1	UTSW	5	96,825,244 (GRCm39)	critical splice donor site	probably null
R4065:Fras1	UTSW	5	96,918,542 (GRCm39)	missense	possibly damaging	0.64
R4066:Fras1	UTSW	5	96,918,542 (GRCm39)	missense	possibly damaging	0.64
R4076:Fras1	UTSW	5	96,891,017 (GRCm39)	missense	probably damaging	1.00
R4124:Fras1	UTSW	5	96,918,512 (GRCm39)	missense	probably benign	0.05
R4127:Fras1	UTSW	5	96,918,512 (GRCm39)	missense	probably benign	0.05
R4153:Fras1	UTSW	5	96,924,594 (GRCm39)	missense	probably benign	0.17
R4233:Fras1	UTSW	5	96,862,235 (GRCm39)	missense	possibly damaging	0.91
R4273:Fras1	UTSW	5	96,762,763 (GRCm39)	missense	probably benign	0.00
R4355:Fras1	UTSW	5	96,848,101 (GRCm39)	missense	probably benign
R4401:Fras1	UTSW	5	96,790,479 (GRCm39)	missense	probably damaging	0.97
R4402:Fras1	UTSW	5	96,790,479 (GRCm39)	missense	probably damaging	0.97
R4403:Fras1	UTSW	5	96,790,479 (GRCm39)	missense	probably damaging	0.97
R4505:Fras1	UTSW	5	96,929,207 (GRCm39)	missense	probably damaging	1.00
R4548:Fras1	UTSW	5	96,857,754 (GRCm39)	missense	probably benign	0.00
R4559:Fras1	UTSW	5	96,929,148 (GRCm39)	missense	probably damaging	1.00
R4629:Fras1	UTSW	5	96,924,593 (GRCm39)	missense	probably benign	0.00
R4637:Fras1	UTSW	5	96,925,947 (GRCm39)	missense	probably damaging	1.00
R4678:Fras1	UTSW	5	96,848,427 (GRCm39)	missense	probably benign	0.13
R4707:Fras1	UTSW	5	96,883,097 (GRCm39)	missense	probably damaging	0.96
R4735:Fras1	UTSW	5	96,736,022 (GRCm39)	missense	probably benign	0.00
R4756:Fras1	UTSW	5	96,929,518 (GRCm39)	missense	probably benign	0.00
R4762:Fras1	UTSW	5	96,879,477 (GRCm39)	missense	probably benign
R4847:Fras1	UTSW	5	96,692,851 (GRCm39)	missense	possibly damaging	0.94
R4857:Fras1	UTSW	5	96,926,018 (GRCm39)	missense	probably benign	0.00
R4909:Fras1	UTSW	5	96,856,617 (GRCm39)	missense	probably benign	0.01
R4931:Fras1	UTSW	5	96,784,699 (GRCm39)	missense	probably benign	0.02
R4938:Fras1	UTSW	5	96,924,583 (GRCm39)	missense	probably damaging	0.99
R4952:Fras1	UTSW	5	96,795,357 (GRCm39)	missense	probably benign	0.01
R4965:Fras1	UTSW	5	96,874,439 (GRCm39)	missense	possibly damaging	0.95
R4989:Fras1	UTSW	5	96,798,541 (GRCm39)	missense	possibly damaging	0.75
R5151:Fras1	UTSW	5	96,792,969 (GRCm39)	missense	probably damaging	1.00
R5168:Fras1	UTSW	5	96,856,616 (GRCm39)	missense	probably benign	0.00
R5182:Fras1	UTSW	5	96,784,032 (GRCm39)	nonsense	probably null
R5214:Fras1	UTSW	5	96,917,452 (GRCm39)	missense	probably damaging	1.00
R5220:Fras1	UTSW	5	96,916,222 (GRCm39)	missense	probably damaging	1.00
R5235:Fras1	UTSW	5	96,748,609 (GRCm39)	missense	probably benign	0.02
R5242:Fras1	UTSW	5	96,805,109 (GRCm39)	missense	probably benign	0.11
R5253:Fras1	UTSW	5	96,888,884 (GRCm39)	missense	probably damaging	0.99
R5260:Fras1	UTSW	5	96,883,046 (GRCm39)	missense	possibly damaging	0.79
R5301:Fras1	UTSW	5	96,805,125 (GRCm39)	missense	possibly damaging	0.88
R5411:Fras1	UTSW	5	96,793,019 (GRCm39)	missense	probably benign	0.00
R5467:Fras1	UTSW	5	96,927,912 (GRCm39)	missense	probably benign	0.04
R5543:Fras1	UTSW	5	96,676,394 (GRCm39)	missense	probably benign	0.01
R5555:Fras1	UTSW	5	96,825,236 (GRCm39)	missense	probably benign	0.34
R5602:Fras1	UTSW	5	96,884,880 (GRCm39)	missense	probably damaging	1.00
R5664:Fras1	UTSW	5	96,876,394 (GRCm39)	missense	possibly damaging	0.91
R5695:Fras1	UTSW	5	96,929,203 (GRCm39)	missense	probably damaging	1.00
R5717:Fras1	UTSW	5	96,929,596 (GRCm39)	missense	possibly damaging	0.93
R5742:Fras1	UTSW	5	96,916,240 (GRCm39)	missense	possibly damaging	0.50
R5759:Fras1	UTSW	5	96,857,775 (GRCm39)	missense	probably benign	0.02
R5766:Fras1	UTSW	5	96,879,548 (GRCm39)	missense	possibly damaging	0.91
R5890:Fras1	UTSW	5	96,793,807 (GRCm39)	missense	probably benign
R6052:Fras1	UTSW	5	96,912,725 (GRCm39)	missense	probably damaging	1.00
R6058:Fras1	UTSW	5	96,857,844 (GRCm39)	missense	probably benign
R6256:Fras1	UTSW	5	96,881,702 (GRCm39)	missense	possibly damaging	0.84
R6306:Fras1	UTSW	5	96,912,805 (GRCm39)	missense	probably damaging	1.00
R6494:Fras1	UTSW	5	96,907,423 (GRCm39)	missense	possibly damaging	0.59
R6638:Fras1	UTSW	5	96,905,953 (GRCm39)	missense	possibly damaging	0.94
R6647:Fras1	UTSW	5	96,883,061 (GRCm39)	missense	probably damaging	1.00
R6725:Fras1	UTSW	5	96,929,199 (GRCm39)	missense	possibly damaging	0.91
R6769:Fras1	UTSW	5	96,746,800 (GRCm39)	missense	possibly damaging	0.60
R6771:Fras1	UTSW	5	96,746,800 (GRCm39)	missense	possibly damaging	0.60
R6837:Fras1	UTSW	5	96,874,832 (GRCm39)	missense	probably damaging	0.99
R6841:Fras1	UTSW	5	96,876,410 (GRCm39)	missense	probably damaging	0.99
R6863:Fras1	UTSW	5	96,691,165 (GRCm39)	missense	probably benign	0.19
R6868:Fras1	UTSW	5	96,830,237 (GRCm39)	missense	probably benign	0.38
R6936:Fras1	UTSW	5	96,916,211 (GRCm39)	missense	possibly damaging	0.92
R6997:Fras1	UTSW	5	96,762,732 (GRCm39)	nonsense	probably null
R7023:Fras1	UTSW	5	96,857,943 (GRCm39)	missense	probably benign	0.00
R7091:Fras1	UTSW	5	96,856,535 (GRCm39)	missense	probably benign
R7102:Fras1	UTSW	5	96,718,900 (GRCm39)	missense	probably benign
R7120:Fras1	UTSW	5	96,900,819 (GRCm39)	nonsense	probably null
R7124:Fras1	UTSW	5	96,862,260 (GRCm39)	missense	probably damaging	1.00
R7129:Fras1	UTSW	5	96,929,143 (GRCm39)	missense	probably benign	0.00
R7173:Fras1	UTSW	5	96,925,937 (GRCm39)	missense	probably damaging	1.00
R7174:Fras1	UTSW	5	96,903,436 (GRCm39)	critical splice donor site	probably null
R7185:Fras1	UTSW	5	96,784,635 (GRCm39)	missense	probably damaging	1.00
R7191:Fras1	UTSW	5	96,762,771 (GRCm39)	missense	probably benign	0.05
R7216:Fras1	UTSW	5	96,887,173 (GRCm39)	missense	probably damaging	1.00
R7222:Fras1	UTSW	5	96,784,668 (GRCm39)	missense	probably benign	0.00
R7222:Fras1	UTSW	5	96,784,045 (GRCm39)	missense	probably damaging	1.00
R7320:Fras1	UTSW	5	96,857,745 (GRCm39)	missense	probably benign	0.03
R7335:Fras1	UTSW	5	96,884,829 (GRCm39)	missense	possibly damaging	0.82
R7378:Fras1	UTSW	5	96,744,644 (GRCm39)	missense	probably damaging	0.98
R7394:Fras1	UTSW	5	96,860,309 (GRCm39)	nonsense	probably null
R7412:Fras1	UTSW	5	96,762,748 (GRCm39)	missense	probably benign	0.06
R7422:Fras1	UTSW	5	96,821,458 (GRCm39)	missense	probably benign	0.21
R7552:Fras1	UTSW	5	96,916,297 (GRCm39)	missense	probably damaging	1.00
R7559:Fras1	UTSW	5	96,888,713 (GRCm39)	missense	possibly damaging	0.82
R7575:Fras1	UTSW	5	96,691,173 (GRCm39)	missense	probably benign	0.02
R7578:Fras1	UTSW	5	96,832,296 (GRCm39)	missense	probably damaging	1.00
R7600:Fras1	UTSW	5	96,832,295 (GRCm39)	missense	probably damaging	1.00
R7669:Fras1	UTSW	5	96,840,483 (GRCm39)	missense	probably benign	0.01
R7710:Fras1	UTSW	5	96,792,962 (GRCm39)	nonsense	probably null
R7722:Fras1	UTSW	5	96,917,413 (GRCm39)	missense	probably damaging	1.00
R7726:Fras1	UTSW	5	96,860,310 (GRCm39)	missense	probably benign	0.41
R7745:Fras1	UTSW	5	96,874,754 (GRCm39)	missense	probably benign	0.11
R7777:Fras1	UTSW	5	96,900,763 (GRCm39)	missense	probably damaging	1.00
R7923:Fras1	UTSW	5	96,887,177 (GRCm39)	missense	probably damaging	1.00
R7925:Fras1	UTSW	5	96,929,443 (GRCm39)	missense	probably damaging	0.96
R8000:Fras1	UTSW	5	96,910,536 (GRCm39)	missense	probably damaging	0.96
R8056:Fras1	UTSW	5	96,892,633 (GRCm39)	missense	probably damaging	1.00
R8058:Fras1	UTSW	5	96,842,778 (GRCm39)	missense	probably benign
R8117:Fras1	UTSW	5	96,855,245 (GRCm39)	missense	probably damaging	1.00
R8157:Fras1	UTSW	5	96,702,714 (GRCm39)	missense	probably benign	0.00
R8312:Fras1	UTSW	5	96,736,050 (GRCm39)	missense	probably benign
R8315:Fras1	UTSW	5	96,891,041 (GRCm39)	missense	probably damaging	0.97
R8412:Fras1	UTSW	5	96,744,711 (GRCm39)	missense	probably benign	0.00
R8546:Fras1	UTSW	5	96,857,825 (GRCm39)	missense	probably benign	0.00
R8705:Fras1	UTSW	5	96,839,260 (GRCm39)	missense	probably benign	0.01
R8790:Fras1	UTSW	5	96,903,236 (GRCm39)	missense	probably damaging	1.00
R8848:Fras1	UTSW	5	96,929,207 (GRCm39)	missense	probably damaging	1.00
R8855:Fras1	UTSW	5	96,917,465 (GRCm39)	missense
R8871:Fras1	UTSW	5	96,855,257 (GRCm39)	missense	probably benign	0.34
R8894:Fras1	UTSW	5	96,907,402 (GRCm39)	missense	probably damaging	1.00
R8904:Fras1	UTSW	5	96,929,138 (GRCm39)	missense	probably benign	0.16
R8910:Fras1	UTSW	5	96,715,855 (GRCm39)	missense	probably benign	0.01
R8916:Fras1	UTSW	5	96,900,774 (GRCm39)	missense	probably damaging	1.00
R8929:Fras1	UTSW	5	96,917,366 (GRCm39)	missense	probably damaging	0.98
R8995:Fras1	UTSW	5	96,860,415 (GRCm39)	missense	possibly damaging	0.83
R9016:Fras1	UTSW	5	96,783,923 (GRCm39)	missense	probably damaging	0.96
R9021:Fras1	UTSW	5	96,888,609 (GRCm39)	missense	probably damaging	1.00
R9038:Fras1	UTSW	5	96,874,742 (GRCm39)	missense	probably benign	0.25
R9204:Fras1	UTSW	5	96,883,022 (GRCm39)	missense	probably damaging	1.00
R9222:Fras1	UTSW	5	96,805,087 (GRCm39)	missense	probably benign	0.15
R9231:Fras1	UTSW	5	96,692,904 (GRCm39)	missense	probably damaging	1.00
R9238:Fras1	UTSW	5	96,832,220 (GRCm39)	missense	possibly damaging	0.90
R9257:Fras1	UTSW	5	96,910,359 (GRCm39)	missense	probably damaging	1.00
R9302:Fras1	UTSW	5	96,682,751 (GRCm39)	missense	probably damaging	1.00
R9329:Fras1	UTSW	5	96,884,813 (GRCm39)	missense	probably damaging	1.00
R9361:Fras1	UTSW	5	96,924,557 (GRCm39)	missense	probably damaging	1.00
R9430:Fras1	UTSW	5	96,929,251 (GRCm39)	missense	probably benign	0.00
R9431:Fras1	UTSW	5	96,900,873 (GRCm39)	missense	possibly damaging	0.71
R9474:Fras1	UTSW	5	96,887,124 (GRCm39)	missense	probably benign	0.00
R9475:Fras1	UTSW	5	96,927,929 (GRCm39)	missense	probably damaging	0.96
R9497:Fras1	UTSW	5	96,884,895 (GRCm39)	missense	probably damaging	1.00
R9597:Fras1	UTSW	5	96,888,551 (GRCm39)	missense	probably damaging	1.00
R9650:Fras1	UTSW	5	96,910,387 (GRCm39)	missense	probably damaging	1.00
R9694:Fras1	UTSW	5	96,929,545 (GRCm39)	missense	probably benign	0.03
R9779:Fras1	UTSW	5	96,717,353 (GRCm39)	missense	probably damaging	0.99
Z1088:Fras1	UTSW	5	96,891,070 (GRCm39)	missense	probably damaging	0.97
Z1088:Fras1	UTSW	5	96,906,001 (GRCm39)	missense	probably benign
Z1176:Fras1	UTSW	5	96,906,001 (GRCm39)	missense	probably benign
Z1177:Fras1	UTSW	5	96,848,110 (GRCm39)	missense	possibly damaging	0.71
Z1177:Fras1	UTSW	5	96,839,316 (GRCm39)	missense	probably damaging	1.00
Z1177:Fras1	UTSW	5	96,906,001 (GRCm39)	missense	probably benign
Z1177:Fras1	UTSW	5	96,888,842 (GRCm39)	missense	possibly damaging	0.95
Z1177:Fras1	UTSW	5	96,888,670 (GRCm39)	missense	probably benign	0.18

Predicted Primers

PCR Primer
(F):5'- AGGCTGAGTCCATCACCTTC -3'
(R):5'- GAAGCCTCAATTATTGTGCCATTG -3'

Sequencing Primer
(F):5'- ATTGTGCAGCCTCCACG -3'
(R):5'- GTGCCATTGTCTTGAAAAACCAAG -3'

Posted On

2016-02-04