Mutagenetix > Incidental Mutation

Incidental Mutation 'R1800:Fras1'

203027

Institutional Source

Beutler Lab

Gene Symbol

Fras1

Ensembl Gene

ENSMUSG00000034687

Gene Name

Fraser extracellular matrix complex subunit 1

Synonyms

bl, E130113P14Rik

MMRRC Submission

039830-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1800 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

96521814-96932587 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 96857741 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 2012 (S2012P)

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: S2012P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000043250
Gene: ENSMUSG00000034687
AA Change: S2012P

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

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.0%
20x: 91.2%

Validation Efficiency

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: 92 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	A	G	3: 137,772,479 (GRCm39)	K556R	probably damaging	Het
4933406P04Rik	A	T	10: 20,186,893 (GRCm39)		probably benign	Het
Acmsd	C	A	1: 127,687,493 (GRCm39)	Y258*	probably null	Het
Adgrf5	A	T	17: 43,761,973 (GRCm39)	I1223F	probably damaging	Het
Afp	C	T	5: 90,638,655 (GRCm39)	P6S	probably benign	Het
Agap2	C	A	10: 126,927,540 (GRCm39)	H1120Q	probably damaging	Het
Angpt1	A	G	15: 42,375,800 (GRCm39)	V152A	probably damaging	Het
Ankrd1	A	T	19: 36,096,759 (GRCm39)	F23I	probably damaging	Het
Armc12	T	C	17: 28,757,869 (GRCm39)	S334P	possibly damaging	Het
Arnt2	C	A	7: 83,924,583 (GRCm39)	D415Y	probably damaging	Het
Cacna1s	G	T	1: 136,004,592 (GRCm39)	V131L	probably benign	Het
Cacna2d2	T	C	9: 107,404,632 (GRCm39)	V1141A	possibly damaging	Het
Cfap61	T	C	2: 145,884,542 (GRCm39)	L580P	probably damaging	Het
Chga	A	T	12: 102,522,164 (GRCm39)	S23C	probably damaging	Het
Chrna5	A	G	9: 54,912,159 (GRCm39)	T320A	probably damaging	Het
Col17a1	G	T	19: 47,639,301 (GRCm39)	N1081K	possibly damaging	Het
Cox7b2	A	T	5: 71,600,406 (GRCm39)	C51S	possibly damaging	Het
Cstdc3	T	A	16: 36,132,895 (GRCm39)	D57E	probably damaging	Het
Cwc22	A	T	2: 77,759,797 (GRCm39)	D83E	possibly damaging	Het
D130043K22Rik	A	C	13: 25,067,877 (GRCm39)	D871A	probably damaging	Het
Dab2	A	T	15: 6,464,948 (GRCm39)	M361L	probably benign	Het
Dnah11	A	C	12: 117,880,523 (GRCm39)	Y3866D	probably damaging	Het
Dnmbp	A	G	19: 43,890,159 (GRCm39)	I536T	probably benign	Het
Ehmt1	A	T	2: 24,774,302 (GRCm39)	S43R	probably damaging	Het
Ercc5	T	C	1: 44,212,540 (GRCm39)	L666P	probably benign	Het
F5	A	G	1: 164,010,403 (GRCm39)	H378R	probably damaging	Het
Fat2	A	T	11: 55,174,718 (GRCm39)	N1998K	probably damaging	Het
Fbxo28	T	C	1: 182,169,099 (GRCm39)	D13G	unknown	Het
Gm5624	T	A	14: 44,799,302 (GRCm39)	N41I	probably damaging	Het
Gm8104	A	G	14: 42,959,028 (GRCm39)	I73V	possibly damaging	Het
Gpr141b	T	C	13: 19,913,849 (GRCm39)		noncoding transcript	Het
Gpr68	G	A	12: 100,845,167 (GRCm39)	P126S	probably damaging	Het
Gucy1a2	A	T	9: 3,582,685 (GRCm39)	T156S	possibly damaging	Het
Hacl1	T	A	14: 31,336,221 (GRCm39)	Y429F	probably damaging	Het
Haus3	A	C	5: 34,320,916 (GRCm39)	L510R	probably damaging	Het
Helq	C	T	5: 100,921,990 (GRCm39)	G738D	probably benign	Het
Hsd3b2	G	C	3: 98,619,553 (GRCm39)	P131A	probably damaging	Het
Il22ra1	G	T	4: 135,475,471 (GRCm39)	C247F	probably benign	Het
Ivl	T	C	3: 92,479,891 (GRCm39)	E58G	unknown	Het
Kcnk9	G	T	15: 72,417,948 (GRCm39)	Q61K	probably benign	Het
Kremen1	CGGG	CGGGGGG	11: 5,151,791 (GRCm39)		probably benign	Het
Loxhd1	G	T	18: 77,490,198 (GRCm39)	A1314S	probably damaging	Het
Lratd1	T	C	12: 14,200,226 (GRCm39)	Y167C	probably damaging	Het
Lrba	A	G	3: 86,259,175 (GRCm39)	I1397V	probably benign	Het
Lrig3	T	A	10: 125,832,920 (GRCm39)		probably null	Het
Lrrc36	A	G	8: 106,176,397 (GRCm39)	D378G	probably damaging	Het
Lrrc49	G	A	9: 60,505,474 (GRCm39)	T527I	probably damaging	Het
Map4k4	C	A	1: 40,062,620 (GRCm39)	T1195K	probably damaging	Het
Mrps33	G	A	6: 39,779,429 (GRCm39)	R89C	probably damaging	Het
Mtor	T	C	4: 148,547,349 (GRCm39)	V444A	probably benign	Het
Myh2	A	G	11: 67,079,764 (GRCm39)	E1046G	probably damaging	Het
Myo15b	G	T	11: 115,771,335 (GRCm39)		probably null	Het
Myo5c	T	C	9: 75,153,446 (GRCm39)	Y111H	probably damaging	Het
Ncoa4-ps	A	T	12: 119,225,506 (GRCm39)		noncoding transcript	Het
Ndufv2	G	C	17: 66,390,481 (GRCm39)	T163R	probably damaging	Het
Nf1	A	G	11: 79,444,794 (GRCm39)	N373S	possibly damaging	Het
Nwd2	A	G	5: 63,962,917 (GRCm39)	M834V	probably benign	Het
Ogfod2	T	C	5: 124,253,019 (GRCm39)	V343A	probably damaging	Het
Or11g2	C	T	14: 50,856,143 (GRCm39)	L155F	probably benign	Het
Or11j4	C	A	14: 50,630,786 (GRCm39)	S191*	probably null	Het
Or3a1b	A	T	11: 74,012,234 (GRCm39)	T40S	probably benign	Het
Or4c115	T	A	2: 88,928,050 (GRCm39)	T74S	probably benign	Het
Or51ag1	T	C	7: 103,155,248 (GRCm39)	I302V	possibly damaging	Het
Or52ab2	T	A	7: 102,969,621 (GRCm39)	M1K	probably null	Het
Or8g34	A	T	9: 39,373,410 (GRCm39)	I228F	probably damaging	Het
Parp1	T	A	1: 180,428,091 (GRCm39)		probably null	Het
Ppp3ca	A	T	3: 136,640,792 (GRCm39)	I448F	probably damaging	Het
Prss44	T	C	9: 110,646,272 (GRCm39)	V333A	probably damaging	Het
Pxk	C	T	14: 8,151,507 (GRCm38)	R441*	probably null	Het
Rars1	A	C	11: 35,716,822 (GRCm39)	D231E	probably benign	Het
Rfc1	T	C	5: 65,421,722 (GRCm39)	Y1059C	probably damaging	Het
Rilpl1	T	A	5: 124,652,719 (GRCm39)	I2F	probably damaging	Het
Sarm1	G	T	11: 78,381,820 (GRCm39)	A221E	possibly damaging	Het
Serpina3f	A	G	12: 104,183,665 (GRCm39)	T176A	probably damaging	Het
Slc22a20	T	C	19: 6,035,695 (GRCm39)	E131G	probably benign	Het
Slc26a11	T	C	11: 119,263,979 (GRCm39)	V343A	probably damaging	Het
Slc2a4	A	G	11: 69,837,133 (GRCm39)	I9T	probably benign	Het
Slc39a6	G	T	18: 24,718,259 (GRCm39)	D599E	probably damaging	Het
Slc5a6	G	T	5: 31,198,020 (GRCm39)	S285*	probably null	Het
Spata9	A	G	13: 76,125,760 (GRCm39)	H81R	probably benign	Het
St7l	A	G	3: 104,826,812 (GRCm39)	E436G	probably damaging	Het
Tecrl	A	G	5: 83,427,077 (GRCm39)	I357T	probably damaging	Het
Thop1	C	T	10: 80,909,043 (GRCm39)	R25C	probably damaging	Het
Tmprss12	A	G	15: 100,190,428 (GRCm39)	E266G	probably benign	Het
Tpgs1	T	A	10: 79,511,344 (GRCm39)	V162D	possibly damaging	Het
Trpa1	C	T	1: 14,944,648 (GRCm39)	R1032Q	probably benign	Het
Tspan12	A	G	6: 21,795,699 (GRCm39)	Y164H	probably damaging	Het
Ubr4	T	C	4: 139,135,274 (GRCm39)	Y869H	probably damaging	Het
Vmn1r21	A	G	6: 57,820,799 (GRCm39)	I215T	probably benign	Het
Zan	A	T	5: 137,384,713 (GRCm39)	S5104T	unknown	Het
Zfp318	T	C	17: 46,722,980 (GRCm39)	V1661A	probably benign	Het
Zfp365	C	T	10: 67,724,772 (GRCm39)	R372K	probably 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
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
R4820:Fras1	UTSW	5	96,876,512 (GRCm39)	missense	probably benign	0.00
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'- CATGGAGTGGGGTTGAATCC -3'
(R):5'- TCCTGTGTCTACATGGAGGC -3'

Sequencing Primer
(F):5'- AGAATTTTAGTCTCAAGGGTGGACC -3'
(R):5'- TGTGTCTACATGGAGGCCATCC -3'

Posted On

2014-06-23