Incidental Mutation 'R5549:Svep1'
ID 435025
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 043106-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5549 (G1)
Quality Score 182
Status Not validated
Chromosome 4
Chromosomal Location 58042796-58206596 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 58057954 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 3284 (S3284G)
Ref Sequence ENSEMBL: ENSMUSP00000045856 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042850]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000042850
AA Change: S3284G

PolyPhen 2 Score 0.317 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000045856
Gene: ENSMUSG00000028369
AA Change: S3284G

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
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 95.9%
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: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik T C 14: 32,384,993 (GRCm39) E324G possibly damaging Het
Acad8 C T 9: 26,896,847 (GRCm39) R204Q probably damaging Het
Adgrg7 T G 16: 56,570,790 (GRCm39) T413P probably damaging Het
Ankrd11 A G 8: 123,617,117 (GRCm39) I2224T probably benign Het
Arhgap23 A G 11: 97,357,394 (GRCm39) D964G probably damaging Het
Atf6b A G 17: 34,870,657 (GRCm39) D367G probably damaging Het
Axdnd1 A G 1: 156,226,104 (GRCm39) L131P probably damaging Het
Bmp8b T C 4: 123,018,278 (GRCm39) V383A probably damaging Het
C5ar2 A G 7: 15,970,868 (GRCm39) V353A probably damaging Het
Ccr5 C A 9: 123,925,408 (GRCm39) A337E probably benign Het
Cftr G A 6: 18,227,953 (GRCm39) V382I probably benign Het
Csmd3 G C 15: 48,048,753 (GRCm39) S446C probably damaging Het
Cyp2d12 A G 15: 82,440,498 (GRCm39) T96A probably benign Het
Diaph3 T G 14: 87,216,106 (GRCm39) I465L probably benign Het
Fabp3 A G 4: 130,209,018 (GRCm39) *134W probably null Het
Fgf22 G T 10: 79,592,696 (GRCm39) M130I probably damaging Het
Flnc G A 6: 29,453,690 (GRCm39) V1792M probably damaging Het
Grik3 G A 4: 125,579,838 (GRCm39) A528T possibly damaging Het
Hecw2 G A 1: 53,964,850 (GRCm39) R659W possibly damaging Het
Hmbs C T 9: 44,250,774 (GRCm39) probably null Het
Ift122 T G 6: 115,868,983 (GRCm39) L490R probably damaging Het
Igkv4-63 T C 6: 69,355,116 (GRCm39) H55R probably damaging Het
Itga4 A T 2: 79,086,611 (GRCm39) N96I probably damaging Het
Kcna7 A T 7: 45,056,063 (GRCm39) H93L probably damaging Het
Klhdc7b A G 15: 89,271,562 (GRCm39) I815V probably benign Het
Lcmt1 G A 7: 123,027,330 (GRCm39) E298K probably damaging Het
Ly6g6f A G 17: 35,302,333 (GRCm39) V68A possibly damaging Het
Map3k8 C T 18: 4,340,762 (GRCm39) C184Y probably damaging Het
Mcemp1 A G 8: 3,718,340 (GRCm39) T183A possibly damaging Het
Mobp T G 9: 119,996,876 (GRCm39) S2R probably damaging Het
Mprip A G 11: 59,651,644 (GRCm39) S1783G probably benign Het
Mterf3 C A 13: 67,076,321 (GRCm39) A129S probably benign Het
Nfkb2 G T 19: 46,296,006 (GRCm39) E170D probably benign Het
Nr2c1 A G 10: 94,003,558 (GRCm39) T239A probably benign Het
Odr4 A G 1: 150,247,909 (GRCm39) S325P possibly damaging Het
Oplah G A 15: 76,182,466 (GRCm39) A963V probably damaging Het
Or13a26 A G 7: 140,284,712 (GRCm39) probably null Het
Parp14 C T 16: 35,661,505 (GRCm39) S1481N probably benign Het
Prxl2a T C 14: 40,726,013 (GRCm39) K44E possibly damaging Het
Rictor C T 15: 6,816,391 (GRCm39) T1221M probably damaging Het
Rpe G A 1: 66,755,163 (GRCm39) D182N probably damaging Het
Slc24a3 C A 2: 145,448,784 (GRCm39) P443T probably damaging Het
Slc25a47 T C 12: 108,822,143 (GRCm39) *311Q probably null Het
Sox2 C G 3: 34,705,142 (GRCm39) A193G probably benign Het
Zfp369 A T 13: 65,445,194 (GRCm39) H779L probably damaging Het
Zfp513 A T 5: 31,357,947 (GRCm39) L144Q possibly damaging Het
Zfp526 T C 7: 24,925,109 (GRCm39) F456S possibly damaging Het
Zfp791 C T 8: 85,836,835 (GRCm39) G343D probably damaging Het
Zfp941 A C 7: 140,388,021 (GRCm39) I664S possibly damaging Het
Zkscan3 A G 13: 21,578,233 (GRCm39) V189A probably damaging 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
R1774:Svep1 UTSW 4 58,146,562 (GRCm39) missense possibly damaging 0.92
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
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'- CCATTTCTGGAGTCCTTGGG -3'
(R):5'- ACTCTGCCAGGGAAGAATTTTG -3'

Sequencing Primer
(F):5'- CGAGACAGGGTTTCTCTGTATAGTCC -3'
(R):5'- CCAGGGAAGAATTTTGATGAAATTAC -3'
Posted On 2016-10-24