Incidental Mutation 'R1774:Svep1'
ID 196898
Institutional Source Beutler Lab
Gene Symbol Svep1
Ensembl Gene ENSMUSG00000028369
Gene Name sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1
Synonyms 1110021D17Rik, Polydom, D430029O09Rik, 4833413O10Rik
MMRRC Submission 039805-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1774 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 58042796-58206596 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 58146562 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 360 (D360G)
Ref Sequence ENSEMBL: ENSMUSP00000045856 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042850]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000042850
AA Change: D360G

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000045856
Gene: ENSMUSG00000028369
AA Change: D360G

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
low complexity region 51 60 N/A INTRINSIC
VWA 82 261 2.18e-32 SMART
Pfam:GCC2_GCC3 311 361 3.4e-14 PFAM
CCP 379 434 3.62e-8 SMART
CCP 439 494 1.78e-16 SMART
CCP 499 559 2.13e-5 SMART
Pfam:HYR 560 642 1.7e-20 PFAM
Pfam:HYR 643 722 4.6e-15 PFAM
CCP 727 787 3.59e-1 SMART
low complexity region 862 873 N/A INTRINSIC
Pfam:GCC2_GCC3 1004 1051 3.2e-16 PFAM
Pfam:GCC2_GCC3 1058 1105 5.4e-19 PFAM
Pfam:GCC2_GCC3 1112 1159 7.7e-19 PFAM
EGF 1195 1228 3.12e-7 SMART
EGF_CA 1230 1266 3.93e-13 SMART
EGF_CA 1268 1304 8.3e-12 SMART
EGF_CA 1306 1342 4.59e-14 SMART
EGF_CA 1344 1380 8.69e-15 SMART
EGF_CA 1382 1418 3.42e-13 SMART
Pfam:Pentaxin 1429 1622 1.8e-28 PFAM
Pfam:Laminin_G_3 1432 1589 1.1e-20 PFAM
CCP 1630 1684 1.71e-9 SMART
CCP 1689 1742 2.31e-15 SMART
EGF_CA 1744 1783 5.23e-9 SMART
CCP 1788 1841 4.62e-15 SMART
CCP 1846 1899 8.29e-17 SMART
CCP 1904 1957 1.1e-12 SMART
CCP 1962 2015 5.6e-14 SMART
CCP 2020 2077 4.15e-8 SMART
CCP 2082 2140 8.11e-11 SMART
CCP 2145 2198 4.38e-16 SMART
CCP 2203 2258 1.69e-8 SMART
CCP 2263 2317 1.42e-15 SMART
CCP 2322 2375 3.1e-7 SMART
CCP 2380 2434 4.55e-14 SMART
CCP 2439 2492 6.95e-10 SMART
CCP 2497 2550 8.88e-17 SMART
CCP 2555 2607 1.7e-13 SMART
CCP 2651 2709 1.02e-7 SMART
CCP 2714 2767 9.6e-13 SMART
CCP 2772 2825 3.64e-13 SMART
CCP 2830 2883 6.63e-16 SMART
CCP 2888 2941 2.76e-13 SMART
CCP 2946 2999 4.41e-12 SMART
CCP 3004 3055 4.25e-5 SMART
CCP 3060 3113 5.15e-13 SMART
CCP 3118 3172 2.11e-9 SMART
CCP 3177 3232 1.02e-7 SMART
CCP 3237 3290 6.19e-16 SMART
CCP 3295 3348 5.35e-11 SMART
CCP 3353 3407 8.43e-9 SMART
CCP 3412 3464 2.44e-14 SMART
EGF 3467 3496 1.28e-3 SMART
EGF 3499 3528 1.15e-5 SMART
EGF 3531 3560 2.85e-1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128783
Predicted Effect noncoding transcript
Transcript: ENSMUST00000149152
Coding Region Coverage
  • 1x: 97.4%
  • 3x: 96.8%
  • 10x: 95.2%
  • 20x: 92.0%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit complete preweaning lethality, edema, abnormal skin coloration, thick epidermis, acanthosis, and tail/limb abnormalities. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 85 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018F24Rik T C 5: 144,982,351 (GRCm39) V312A probably damaging Het
2810408A11Rik A G 11: 69,791,453 (GRCm39) V42A probably damaging Het
Akap8l C T 17: 32,551,457 (GRCm39) R511H probably damaging Het
Angpt1 T A 15: 42,387,012 (GRCm39) Q114L probably damaging Het
Apc2 T C 10: 80,144,964 (GRCm39) I625T probably damaging Het
Atg2a T C 19: 6,300,628 (GRCm39) V735A probably benign Het
Birc6 T A 17: 74,947,008 (GRCm39) I2909N probably damaging Het
C7 C G 15: 5,041,557 (GRCm39) D450H probably damaging Het
Cachd1 C T 4: 100,821,632 (GRCm39) T403I probably damaging Het
Cachd1 T A 4: 100,824,240 (GRCm39) F560L probably benign Het
Cacna2d2 A T 9: 107,403,350 (GRCm39) Y944F probably benign Het
Cdkal1 C T 13: 30,034,031 (GRCm39) D21N probably damaging Het
Col18a1 T C 10: 76,895,815 (GRCm39) R901G probably damaging Het
Col27a1 C T 4: 63,143,950 (GRCm39) P546L probably damaging Het
Cps1 C T 1: 67,210,041 (GRCm39) R624W possibly damaging Het
Cyp11a1 A T 9: 57,925,643 (GRCm39) I93F probably benign Het
Cyp2c40 G C 19: 39,775,250 (GRCm39) T334R probably damaging Het
Cyp4f37 A G 17: 32,848,864 (GRCm39) D244G possibly damaging Het
D630003M21Rik A T 2: 158,062,390 (GRCm39) D43E probably damaging Het
Ep400 C A 5: 110,833,357 (GRCm39) C1955F unknown Het
Ethe1 G A 7: 24,293,371 (GRCm39) V6I probably benign Het
F5 C A 1: 164,020,104 (GRCm39) Q860K probably benign Het
Fasn T C 11: 120,707,997 (GRCm39) Y685C probably damaging Het
Gga2 T G 7: 121,611,444 (GRCm39) D38A probably damaging Het
Gm43302 T A 5: 105,423,660 (GRCm39) I438F probably benign Het
Grm1 T A 10: 10,955,610 (GRCm39) T225S possibly damaging Het
Hic2 G T 16: 17,076,511 (GRCm39) V447L probably damaging Het
Hsf2 G A 10: 57,388,242 (GRCm39) C462Y probably damaging Het
Ice1 T C 13: 70,752,672 (GRCm39) D1138G probably damaging Het
Il6 A G 5: 30,224,433 (GRCm39) T158A probably benign Het
Inpp5d T A 1: 87,595,611 (GRCm39) V120E probably benign Het
Iqca1 T C 1: 90,008,625 (GRCm39) N456S probably benign Het
Itgal T A 7: 126,908,794 (GRCm39) probably null Het
Lrrc66 G C 5: 73,768,198 (GRCm39) Q248E probably benign Het
Lrrc7 T A 3: 157,865,929 (GRCm39) M1271L possibly damaging Het
Lrrc74a T C 12: 86,795,827 (GRCm39) S267P probably damaging Het
Map2 T C 1: 66,453,233 (GRCm39) S550P probably damaging Het
Mapk8ip3 A T 17: 25,143,119 (GRCm39) probably null Het
Mdm4 A C 1: 132,924,384 (GRCm39) S246A probably damaging Het
Med23 A G 10: 24,779,584 (GRCm39) E887G probably damaging Het
Mta1 C T 12: 113,091,659 (GRCm39) A254V probably damaging Het
Myh2 A G 11: 67,064,300 (GRCm39) Y85C possibly damaging Het
Myo1g A G 11: 6,465,988 (GRCm39) Y366H probably damaging Het
Nalcn G A 14: 123,515,678 (GRCm39) P1708S probably benign Het
Nlrp9c A T 7: 26,093,543 (GRCm39) S41T probably benign Het
Nptx2 T A 5: 144,490,248 (GRCm39) S226T possibly damaging Het
Nup85 T A 11: 115,473,771 (GRCm39) S562T probably benign Het
Nxpe5 T C 5: 138,237,797 (GRCm39) V107A probably benign Het
Obi1 A G 14: 104,717,098 (GRCm39) V425A possibly damaging Het
Oga T C 19: 45,765,423 (GRCm39) E128G probably benign Het
Or10ac1 A T 6: 42,515,453 (GRCm39) F168I probably damaging Het
Or10al7 A G 17: 38,366,328 (GRCm39) V43A probably benign Het
Or13c3 T A 4: 52,855,674 (GRCm39) I280F probably benign Het
Or6p1 A G 1: 174,258,905 (GRCm39) T304A probably benign Het
Pcdhb12 C T 18: 37,569,495 (GRCm39) P214S possibly damaging Het
Pcdhb5 T A 18: 37,455,725 (GRCm39) F702I probably damaging Het
Pcnx1 T C 12: 82,022,094 (GRCm39) F1475S probably damaging Het
Pde5a C A 3: 122,523,013 (GRCm39) T40N probably benign Het
Pnpla2 T A 7: 141,039,481 (GRCm39) V398E probably damaging Het
Pramel19 G A 4: 101,797,655 (GRCm39) V18M probably benign Het
Pwwp4a G T X: 72,171,261 (GRCm39) G218C probably damaging Het
Rab20 T C 8: 11,504,223 (GRCm39) K159R probably benign Het
Rfwd3 C T 8: 112,014,874 (GRCm39) R326Q probably damaging Het
Rgs12 T A 5: 35,123,747 (GRCm39) V510D probably benign Het
Slamf6 T C 1: 171,770,154 (GRCm39) probably benign Het
Slc27a5 A T 7: 12,731,534 (GRCm39) C23* probably null Het
Slc35e2 T C 4: 155,694,621 (GRCm39) V56A possibly damaging Het
Slx4ip T C 2: 136,909,643 (GRCm39) S143P probably damaging Het
Stat5a C T 11: 100,770,112 (GRCm39) S463F probably damaging Het
Tas2r143 A T 6: 42,377,305 (GRCm39) D45V probably damaging Het
Tdrd5 G T 1: 156,105,079 (GRCm39) R516S probably damaging Het
Thy1 A G 9: 43,958,636 (GRCm39) D126G probably benign Het
Tspear C T 10: 77,709,019 (GRCm39) T415I probably benign Het
Ttll5 C A 12: 85,980,176 (GRCm39) T920K probably benign Het
Tut4 T C 4: 108,365,152 (GRCm39) F542L probably damaging Het
Umod T C 7: 119,076,574 (GRCm39) E64G possibly damaging Het
Usf3 A G 16: 44,036,033 (GRCm39) N171S probably damaging Het
Vmn1r23 T A 6: 57,903,675 (GRCm39) R34S probably damaging Het
Wasf1 C G 10: 40,810,475 (GRCm39) P239R possibly damaging Het
Wdr95 C T 5: 149,487,857 (GRCm39) R164* probably null Het
Zan C A 5: 137,418,251 (GRCm39) C2949F unknown Het
Zbed4 T C 15: 88,665,080 (GRCm39) S383P probably benign Het
Zfand5 T A 19: 21,253,895 (GRCm39) C33S probably damaging Het
Zfp12 A G 5: 143,230,984 (GRCm39) Y437C probably damaging Het
Zfp451 A C 1: 33,852,849 (GRCm39) S22A probably benign Het
Other mutations in Svep1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00475:Svep1 APN 4 58,176,077 (GRCm39) missense probably damaging 0.98
IGL00489:Svep1 APN 4 58,068,988 (GRCm39) missense possibly damaging 0.71
IGL00496:Svep1 APN 4 58,069,001 (GRCm39) missense possibly damaging 0.95
IGL00864:Svep1 APN 4 58,068,533 (GRCm39) nonsense probably null
IGL00904:Svep1 APN 4 58,097,398 (GRCm39) missense probably benign 0.00
IGL00935:Svep1 APN 4 58,090,664 (GRCm39) missense possibly damaging 0.71
IGL00963:Svep1 APN 4 58,072,791 (GRCm39) nonsense probably null
IGL01077:Svep1 APN 4 58,068,760 (GRCm39) missense possibly damaging 0.71
IGL01084:Svep1 APN 4 58,111,419 (GRCm39) missense possibly damaging 0.71
IGL01150:Svep1 APN 4 58,070,302 (GRCm39) missense probably benign 0.04
IGL01161:Svep1 APN 4 58,146,569 (GRCm39) missense probably damaging 0.96
IGL01360:Svep1 APN 4 58,116,554 (GRCm39) missense possibly damaging 0.73
IGL01365:Svep1 APN 4 58,100,878 (GRCm39) critical splice acceptor site probably null
IGL01396:Svep1 APN 4 58,068,552 (GRCm39) missense possibly damaging 0.85
IGL01601:Svep1 APN 4 58,084,872 (GRCm39) missense probably damaging 1.00
IGL01636:Svep1 APN 4 58,116,622 (GRCm39) missense possibly damaging 0.96
IGL01838:Svep1 APN 4 58,121,910 (GRCm39) missense possibly damaging 0.72
IGL01949:Svep1 APN 4 58,176,006 (GRCm39) missense probably damaging 1.00
IGL01984:Svep1 APN 4 58,068,877 (GRCm39) missense possibly damaging 0.93
IGL02005:Svep1 APN 4 58,069,056 (GRCm39) missense possibly damaging 0.93
IGL02036:Svep1 APN 4 58,088,245 (GRCm39) missense possibly damaging 0.85
IGL02039:Svep1 APN 4 58,123,980 (GRCm39) critical splice donor site probably null
IGL02043:Svep1 APN 4 58,068,556 (GRCm39) missense probably benign 0.19
IGL02073:Svep1 APN 4 58,070,104 (GRCm39) missense probably benign 0.06
IGL02188:Svep1 APN 4 58,068,382 (GRCm39) missense possibly damaging 0.71
IGL02256:Svep1 APN 4 58,070,311 (GRCm39) missense possibly damaging 0.71
IGL02284:Svep1 APN 4 58,072,819 (GRCm39) missense probably benign 0.32
IGL02323:Svep1 APN 4 58,070,236 (GRCm39) nonsense probably null
IGL02440:Svep1 APN 4 58,145,293 (GRCm39) missense probably benign 0.06
IGL02449:Svep1 APN 4 58,070,296 (GRCm39) missense possibly damaging 0.71
IGL02501:Svep1 APN 4 58,145,341 (GRCm39) splice site probably benign
IGL02568:Svep1 APN 4 58,135,441 (GRCm39) missense probably benign 0.42
IGL02625:Svep1 APN 4 58,115,807 (GRCm39) missense possibly damaging 0.53
IGL02795:Svep1 APN 4 58,123,223 (GRCm39) missense probably damaging 1.00
IGL02818:Svep1 APN 4 58,069,804 (GRCm39) missense possibly damaging 0.71
IGL02871:Svep1 APN 4 58,100,871 (GRCm39) missense probably benign
IGL02875:Svep1 APN 4 58,082,821 (GRCm39) splice site probably benign
IGL02887:Svep1 APN 4 58,145,301 (GRCm39) missense probably damaging 1.00
IGL03240:Svep1 APN 4 58,048,188 (GRCm39) missense possibly damaging 0.73
IGL03243:Svep1 APN 4 58,133,387 (GRCm39) missense probably benign 0.06
IGL03264:Svep1 APN 4 58,066,422 (GRCm39) splice site probably benign
IGL03288:Svep1 APN 4 58,116,532 (GRCm39) missense probably benign 0.01
IGL03340:Svep1 APN 4 58,111,451 (GRCm39) missense possibly damaging 0.96
IGL03341:Svep1 APN 4 58,070,308 (GRCm39) nonsense probably null
IGL03348:Svep1 APN 4 58,113,635 (GRCm39) missense probably damaging 1.00
R0001:Svep1 UTSW 4 58,066,460 (GRCm39) missense possibly damaging 0.93
R0042:Svep1 UTSW 4 58,123,192 (GRCm39) missense possibly damaging 0.92
R0042:Svep1 UTSW 4 58,123,192 (GRCm39) missense possibly damaging 0.92
R0125:Svep1 UTSW 4 58,099,937 (GRCm39) splice site probably benign
R0142:Svep1 UTSW 4 58,118,232 (GRCm39) missense probably benign 0.33
R0147:Svep1 UTSW 4 58,116,608 (GRCm39) missense possibly damaging 0.85
R0148:Svep1 UTSW 4 58,116,608 (GRCm39) missense possibly damaging 0.85
R0157:Svep1 UTSW 4 58,069,830 (GRCm39) missense possibly damaging 0.72
R0195:Svep1 UTSW 4 58,089,514 (GRCm39) missense possibly damaging 0.82
R0197:Svep1 UTSW 4 58,070,851 (GRCm39) missense possibly damaging 0.71
R0257:Svep1 UTSW 4 58,179,610 (GRCm39) missense possibly damaging 0.71
R0314:Svep1 UTSW 4 58,096,331 (GRCm39) missense possibly damaging 0.71
R0316:Svep1 UTSW 4 58,072,737 (GRCm39) missense probably damaging 0.98
R0322:Svep1 UTSW 4 58,057,996 (GRCm39) splice site probably benign
R0426:Svep1 UTSW 4 58,073,333 (GRCm39) missense possibly damaging 0.87
R0446:Svep1 UTSW 4 58,088,280 (GRCm39) missense probably damaging 1.00
R0457:Svep1 UTSW 4 58,118,136 (GRCm39) missense probably damaging 1.00
R0471:Svep1 UTSW 4 58,054,700 (GRCm39) missense possibly damaging 0.85
R0555:Svep1 UTSW 4 58,128,858 (GRCm39) missense possibly damaging 0.71
R0634:Svep1 UTSW 4 58,070,661 (GRCm39) missense possibly damaging 0.86
R0636:Svep1 UTSW 4 58,073,121 (GRCm39) nonsense probably null
R0827:Svep1 UTSW 4 58,053,113 (GRCm39) splice site probably benign
R1025:Svep1 UTSW 4 58,087,817 (GRCm39) missense possibly damaging 0.86
R1027:Svep1 UTSW 4 58,094,084 (GRCm39) missense possibly damaging 0.86
R1069:Svep1 UTSW 4 58,070,239 (GRCm39) missense probably damaging 1.00
R1161:Svep1 UTSW 4 58,069,416 (GRCm39) missense possibly damaging 0.71
R1245:Svep1 UTSW 4 58,066,427 (GRCm39) critical splice donor site probably null
R1282:Svep1 UTSW 4 58,100,032 (GRCm39) missense possibly damaging 0.93
R1310:Svep1 UTSW 4 58,069,416 (GRCm39) missense possibly damaging 0.71
R1444:Svep1 UTSW 4 58,115,754 (GRCm39) missense possibly damaging 0.53
R1460:Svep1 UTSW 4 58,068,740 (GRCm39) missense possibly damaging 0.85
R1500:Svep1 UTSW 4 58,070,239 (GRCm39) missense probably damaging 1.00
R1628:Svep1 UTSW 4 58,107,561 (GRCm39) missense probably benign 0.00
R1712:Svep1 UTSW 4 58,070,629 (GRCm39) missense probably benign 0.06
R1783:Svep1 UTSW 4 58,073,333 (GRCm39) missense probably benign
R1829:Svep1 UTSW 4 58,096,310 (GRCm39) missense possibly damaging 0.93
R1978:Svep1 UTSW 4 58,097,292 (GRCm39) missense possibly damaging 0.73
R1993:Svep1 UTSW 4 58,064,170 (GRCm39) critical splice donor site probably null
R2017:Svep1 UTSW 4 58,070,568 (GRCm39) missense probably benign 0.08
R2058:Svep1 UTSW 4 58,084,554 (GRCm39) missense possibly damaging 0.92
R2109:Svep1 UTSW 4 58,206,030 (GRCm39) missense possibly damaging 0.51
R2215:Svep1 UTSW 4 58,138,602 (GRCm39) splice site probably benign
R2281:Svep1 UTSW 4 58,082,677 (GRCm39) missense possibly damaging 0.85
R2504:Svep1 UTSW 4 58,135,628 (GRCm39) splice site probably null
R2763:Svep1 UTSW 4 58,084,061 (GRCm39) missense possibly damaging 0.86
R3122:Svep1 UTSW 4 58,087,845 (GRCm39) missense possibly damaging 0.51
R3605:Svep1 UTSW 4 58,066,542 (GRCm39) missense probably benign 0.32
R3763:Svep1 UTSW 4 58,084,833 (GRCm39) missense possibly damaging 0.89
R3827:Svep1 UTSW 4 58,096,177 (GRCm39) missense probably damaging 0.98
R3829:Svep1 UTSW 4 58,096,177 (GRCm39) missense probably damaging 0.98
R3830:Svep1 UTSW 4 58,096,177 (GRCm39) missense probably damaging 0.98
R3910:Svep1 UTSW 4 58,145,156 (GRCm39) critical splice donor site probably null
R3943:Svep1 UTSW 4 58,084,807 (GRCm39) splice site probably null
R3944:Svep1 UTSW 4 58,084,807 (GRCm39) splice site probably null
R4153:Svep1 UTSW 4 58,089,426 (GRCm39) missense possibly damaging 0.52
R4154:Svep1 UTSW 4 58,069,068 (GRCm39) missense possibly damaging 0.71
R4191:Svep1 UTSW 4 58,046,601 (GRCm39) missense possibly damaging 0.86
R4355:Svep1 UTSW 4 58,138,695 (GRCm39) missense possibly damaging 0.71
R4388:Svep1 UTSW 4 58,069,249 (GRCm39) missense possibly damaging 0.93
R4532:Svep1 UTSW 4 58,068,886 (GRCm39) missense possibly damaging 0.52
R4584:Svep1 UTSW 4 58,068,526 (GRCm39) nonsense probably null
R4592:Svep1 UTSW 4 58,084,028 (GRCm39) missense possibly damaging 0.93
R4593:Svep1 UTSW 4 58,091,944 (GRCm39) missense possibly damaging 0.71
R4625:Svep1 UTSW 4 58,072,698 (GRCm39) missense probably damaging 0.98
R4639:Svep1 UTSW 4 58,082,724 (GRCm39) missense probably benign
R4700:Svep1 UTSW 4 58,097,323 (GRCm39) missense possibly damaging 0.71
R4720:Svep1 UTSW 4 58,205,869 (GRCm39) missense possibly damaging 0.71
R4724:Svep1 UTSW 4 58,070,752 (GRCm39) missense possibly damaging 0.71
R4753:Svep1 UTSW 4 58,053,212 (GRCm39) missense probably benign 0.06
R4781:Svep1 UTSW 4 58,070,340 (GRCm39) missense probably damaging 0.98
R4820:Svep1 UTSW 4 58,082,664 (GRCm39) missense probably benign 0.27
R4896:Svep1 UTSW 4 58,087,751 (GRCm39) missense probably benign 0.08
R4905:Svep1 UTSW 4 58,069,308 (GRCm39) missense probably benign 0.00
R4910:Svep1 UTSW 4 58,096,276 (GRCm39) missense possibly damaging 0.71
R4972:Svep1 UTSW 4 58,087,778 (GRCm39) missense possibly damaging 0.71
R5004:Svep1 UTSW 4 58,087,751 (GRCm39) missense probably benign 0.08
R5088:Svep1 UTSW 4 58,120,648 (GRCm39) missense possibly damaging 0.73
R5112:Svep1 UTSW 4 58,068,610 (GRCm39) nonsense probably null
R5185:Svep1 UTSW 4 58,084,534 (GRCm39) missense probably damaging 0.99
R5302:Svep1 UTSW 4 58,096,183 (GRCm39) missense possibly damaging 0.71
R5307:Svep1 UTSW 4 58,072,677 (GRCm39) missense possibly damaging 0.71
R5339:Svep1 UTSW 4 58,121,892 (GRCm39) missense possibly damaging 0.96
R5379:Svep1 UTSW 4 58,072,991 (GRCm39) missense possibly damaging 0.51
R5384:Svep1 UTSW 4 58,104,545 (GRCm39) missense possibly damaging 0.71
R5414:Svep1 UTSW 4 58,206,322 (GRCm39) missense possibly damaging 0.53
R5514:Svep1 UTSW 4 58,044,054 (GRCm39) missense possibly damaging 0.53
R5538:Svep1 UTSW 4 58,049,282 (GRCm39) critical splice acceptor site probably null
R5549:Svep1 UTSW 4 58,057,954 (GRCm39) missense probably benign 0.32
R5618:Svep1 UTSW 4 58,070,537 (GRCm39) missense probably benign
R5623:Svep1 UTSW 4 58,091,964 (GRCm39) missense possibly damaging 0.92
R5686:Svep1 UTSW 4 58,072,826 (GRCm39) missense possibly damaging 0.71
R5743:Svep1 UTSW 4 58,096,223 (GRCm39) missense possibly damaging 0.71
R5773:Svep1 UTSW 4 58,099,985 (GRCm39) missense possibly damaging 0.86
R5809:Svep1 UTSW 4 58,116,524 (GRCm39) missense possibly damaging 0.73
R5896:Svep1 UTSW 4 58,084,906 (GRCm39) missense possibly damaging 0.71
R5918:Svep1 UTSW 4 58,069,345 (GRCm39) missense possibly damaging 0.71
R5969:Svep1 UTSW 4 58,070,977 (GRCm39) nonsense probably null
R6010:Svep1 UTSW 4 58,115,832 (GRCm39) missense possibly damaging 0.95
R6187:Svep1 UTSW 4 58,072,872 (GRCm39) missense probably damaging 1.00
R6192:Svep1 UTSW 4 58,104,536 (GRCm39) missense possibly damaging 0.92
R6209:Svep1 UTSW 4 58,128,869 (GRCm39) missense probably benign 0.32
R6234:Svep1 UTSW 4 58,113,458 (GRCm39) splice site probably null
R6326:Svep1 UTSW 4 58,073,045 (GRCm39) missense possibly damaging 0.51
R6400:Svep1 UTSW 4 58,049,169 (GRCm39) missense probably damaging 1.00
R6418:Svep1 UTSW 4 58,053,126 (GRCm39) missense probably benign 0.01
R6440:Svep1 UTSW 4 58,116,555 (GRCm39) missense possibly damaging 0.53
R6489:Svep1 UTSW 4 58,100,066 (GRCm39) missense probably damaging 1.00
R6515:Svep1 UTSW 4 58,088,280 (GRCm39) missense probably damaging 1.00
R6738:Svep1 UTSW 4 58,123,180 (GRCm39) missense possibly damaging 0.71
R6773:Svep1 UTSW 4 58,049,146 (GRCm39) missense possibly damaging 0.71
R6796:Svep1 UTSW 4 58,064,275 (GRCm39) missense probably benign 0.01
R7055:Svep1 UTSW 4 58,120,642 (GRCm39) missense probably benign 0.33
R7055:Svep1 UTSW 4 58,064,275 (GRCm39) missense probably benign 0.19
R7111:Svep1 UTSW 4 58,118,207 (GRCm39) missense possibly damaging 0.70
R7161:Svep1 UTSW 4 58,128,859 (GRCm39) missense possibly damaging 0.93
R7162:Svep1 UTSW 4 58,070,262 (GRCm39) missense possibly damaging 0.71
R7182:Svep1 UTSW 4 58,043,991 (GRCm39) missense probably benign 0.18
R7292:Svep1 UTSW 4 58,111,395 (GRCm39) missense possibly damaging 0.71
R7299:Svep1 UTSW 4 58,046,587 (GRCm39) nonsense probably null
R7301:Svep1 UTSW 4 58,046,587 (GRCm39) nonsense probably null
R7316:Svep1 UTSW 4 58,068,763 (GRCm39) missense possibly damaging 0.71
R7337:Svep1 UTSW 4 58,108,323 (GRCm39) missense probably damaging 0.98
R7391:Svep1 UTSW 4 58,145,185 (GRCm39) missense probably damaging 0.98
R7402:Svep1 UTSW 4 58,069,699 (GRCm39) missense possibly damaging 0.71
R7445:Svep1 UTSW 4 58,094,122 (GRCm39) missense possibly damaging 0.85
R7450:Svep1 UTSW 4 58,064,248 (GRCm39) missense possibly damaging 0.71
R7492:Svep1 UTSW 4 58,066,468 (GRCm39) missense possibly damaging 0.51
R7505:Svep1 UTSW 4 58,115,862 (GRCm39) missense possibly damaging 0.53
R7509:Svep1 UTSW 4 58,090,683 (GRCm39) missense probably benign 0.40
R7538:Svep1 UTSW 4 58,053,260 (GRCm39) missense possibly damaging 0.71
R7555:Svep1 UTSW 4 58,069,422 (GRCm39) missense probably damaging 0.98
R7660:Svep1 UTSW 4 58,087,782 (GRCm39) missense probably benign 0.32
R7670:Svep1 UTSW 4 58,097,424 (GRCm39) missense probably damaging 1.00
R7719:Svep1 UTSW 4 58,068,523 (GRCm39) missense probably damaging 0.97
R7733:Svep1 UTSW 4 58,049,239 (GRCm39) missense probably benign 0.03
R7781:Svep1 UTSW 4 58,069,251 (GRCm39) missense possibly damaging 0.71
R7821:Svep1 UTSW 4 58,179,601 (GRCm39) missense probably damaging 0.99
R7832:Svep1 UTSW 4 58,054,539 (GRCm39) missense probably benign 0.44
R8017:Svep1 UTSW 4 58,146,637 (GRCm39) missense probably damaging 0.99
R8019:Svep1 UTSW 4 58,146,637 (GRCm39) missense probably damaging 0.99
R8066:Svep1 UTSW 4 58,113,650 (GRCm39) missense probably benign 0.33
R8159:Svep1 UTSW 4 58,087,815 (GRCm39) missense probably benign 0.01
R8159:Svep1 UTSW 4 58,069,396 (GRCm39) missense possibly damaging 0.71
R8170:Svep1 UTSW 4 58,069,378 (GRCm39) missense probably benign 0.00
R8246:Svep1 UTSW 4 58,091,889 (GRCm39) missense probably damaging 0.96
R8392:Svep1 UTSW 4 58,070,566 (GRCm39) missense possibly damaging 0.71
R8436:Svep1 UTSW 4 58,044,053 (GRCm39) missense possibly damaging 0.86
R8544:Svep1 UTSW 4 58,206,025 (GRCm39) missense probably benign 0.00
R8669:Svep1 UTSW 4 58,070,119 (GRCm39) missense possibly damaging 0.95
R8707:Svep1 UTSW 4 58,070,197 (GRCm39) nonsense probably null
R8790:Svep1 UTSW 4 58,118,145 (GRCm39) missense possibly damaging 0.53
R8804:Svep1 UTSW 4 58,206,043 (GRCm39) missense possibly damaging 0.86
R8868:Svep1 UTSW 4 58,135,578 (GRCm39) missense possibly damaging 0.77
R8880:Svep1 UTSW 4 58,064,204 (GRCm39) missense possibly damaging 0.51
R8949:Svep1 UTSW 4 58,054,604 (GRCm39) missense possibly damaging 0.85
R9007:Svep1 UTSW 4 58,091,915 (GRCm39) missense possibly damaging 0.86
R9028:Svep1 UTSW 4 58,145,199 (GRCm39) missense possibly damaging 0.92
R9131:Svep1 UTSW 4 58,087,778 (GRCm39) missense possibly damaging 0.71
R9285:Svep1 UTSW 4 58,084,809 (GRCm39) critical splice donor site probably null
R9302:Svep1 UTSW 4 58,120,565 (GRCm39) missense possibly damaging 0.53
R9314:Svep1 UTSW 4 58,070,347 (GRCm39) missense probably damaging 1.00
R9427:Svep1 UTSW 4 58,069,804 (GRCm39) missense possibly damaging 0.71
R9443:Svep1 UTSW 4 58,179,697 (GRCm39) missense possibly damaging 0.95
R9473:Svep1 UTSW 4 58,064,243 (GRCm39) missense probably benign 0.00
R9487:Svep1 UTSW 4 58,070,517 (GRCm39) missense probably benign
R9494:Svep1 UTSW 4 58,070,577 (GRCm39) missense possibly damaging 0.51
R9515:Svep1 UTSW 4 58,084,144 (GRCm39) missense possibly damaging 0.71
R9681:Svep1 UTSW 4 58,084,959 (GRCm39) missense probably damaging 0.98
X0063:Svep1 UTSW 4 58,070,468 (GRCm39) nonsense probably null
Z1176:Svep1 UTSW 4 58,133,415 (GRCm39) missense possibly damaging 0.51
Z1176:Svep1 UTSW 4 58,115,814 (GRCm39) missense possibly damaging 0.93
Z1176:Svep1 UTSW 4 58,111,386 (GRCm39) missense probably damaging 0.97
Z1177:Svep1 UTSW 4 58,206,300 (GRCm39) missense probably damaging 0.99
Z1177:Svep1 UTSW 4 58,115,841 (GRCm39) missense possibly damaging 0.91
Predicted Primers PCR Primer
(F):5'- ACATTACTCTTATGGCCTCAGATCCCG -3'
(R):5'- GTGGACCAAAGAGACCTTTACACTCAG -3'

Sequencing Primer
(F):5'- CTCTGAACCATGATGCTTATGTG -3'
(R):5'- gctgcttttccaggggac -3'
Posted On 2014-05-23