Incidental Mutation 'R1712:Svep1'
ID 190657
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 039745-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1712 (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 58070629 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 2386 (I2386V)
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: I2386V

PolyPhen 2 Score 0.061 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000045856
Gene: ENSMUSG00000028369
AA Change: I2386V

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: 99.1%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.2%
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: 83 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Accs T A 2: 93,678,448 (GRCm39) E12D probably damaging Het
Ahnak2 C A 12: 112,748,998 (GRCm39) R283L probably benign Het
BC005624 T C 2: 30,864,020 (GRCm39) E191G probably damaging Het
C1galt1 A G 6: 7,871,217 (GRCm39) N351S probably benign Het
Ccdc162 T C 10: 41,415,427 (GRCm39) R2179G probably benign Het
Ccdc88c G A 12: 100,905,284 (GRCm39) T1108M probably benign Het
Cd47 T C 16: 49,714,543 (GRCm39) L184P probably damaging Het
Cdc40 T C 10: 40,717,372 (GRCm39) K440E probably damaging Het
Cenpe G A 3: 134,971,694 (GRCm39) V2262I probably damaging Het
Cep290 A G 10: 100,390,361 (GRCm39) K2035E probably benign Het
Cks1brt G T 8: 85,898,172 (GRCm39) L8F probably benign Het
Col17a1 T C 19: 47,637,442 (GRCm39) probably benign Het
Coro6 A T 11: 77,360,293 (GRCm39) N421I probably benign Het
Cps1 T C 1: 67,269,440 (GRCm39) S1480P probably damaging Het
Csrnp3 G T 2: 65,832,826 (GRCm39) A110S probably damaging Het
Cyp2d10 G T 15: 82,287,240 (GRCm39) T461K probably damaging Het
Dmxl2 A G 9: 54,308,769 (GRCm39) V1994A probably benign Het
Dnah11 T A 12: 118,160,379 (GRCm39) N117I probably benign Het
Dnajc3 A G 14: 119,195,307 (GRCm39) Y74C probably damaging Het
Fam13c T A 10: 70,390,403 (GRCm39) F555I possibly damaging Het
Fbn1 T A 2: 125,188,354 (GRCm39) D1495V probably damaging Het
Fbrsl1 T C 5: 110,595,862 (GRCm39) T58A probably benign Het
Gjd3 A G 11: 102,691,706 (GRCm39) I99T possibly damaging Het
Glce T C 9: 61,977,857 (GRCm39) N9S probably damaging Het
Gosr1 T C 11: 76,641,704 (GRCm39) T125A possibly damaging Het
Ifi27l2a T A 12: 103,406,202 (GRCm39) probably null Het
Jph1 C T 1: 17,167,456 (GRCm39) D125N possibly damaging Het
Kbtbd12 A T 6: 88,595,676 (GRCm39) S51R probably damaging Het
Klra9 A T 6: 130,166,659 (GRCm39) probably null Het
Kmo A T 1: 175,484,289 (GRCm39) M340L probably benign Het
Lama1 T C 17: 68,024,181 (GRCm39) I93T possibly damaging Het
Limk2 A T 11: 3,308,104 (GRCm39) probably null Het
Mgat5 C A 1: 127,248,375 (GRCm39) N92K probably benign Het
Mib2 T A 4: 155,739,256 (GRCm39) I908F probably damaging Het
Mical1 T G 10: 41,356,359 (GRCm39) L304R probably damaging Het
Mtbp G T 15: 55,434,690 (GRCm39) probably null Het
Myo3a T C 2: 22,455,004 (GRCm39) Y70H probably damaging Het
Neb T C 2: 52,133,401 (GRCm39) Y3379C probably damaging Het
Neurod2 G T 11: 98,218,029 (GRCm39) N378K probably damaging Het
Oog4 G A 4: 143,166,484 (GRCm39) L107F probably damaging Het
Or2g25 A G 17: 37,970,799 (GRCm39) S142P probably benign Het
Or4k40 T A 2: 111,251,003 (GRCm39) M98L probably benign Het
Or6x1 A G 9: 40,099,161 (GRCm39) Y250C probably damaging Het
Or8k20 T A 2: 86,106,337 (GRCm39) T165S probably damaging Het
Pfdn6 T C 17: 34,158,528 (GRCm39) Y82C probably damaging Het
Pla2g4d C A 2: 120,107,971 (GRCm39) A313S possibly damaging Het
Ptcd3 C A 6: 71,885,637 (GRCm39) E30* probably null Het
Rai1 A G 11: 60,078,428 (GRCm39) T831A probably benign Het
Rims1 G A 1: 22,367,172 (GRCm39) T1176M probably damaging Het
Rin1 A C 19: 5,105,171 (GRCm39) I744L probably benign Het
Rora T A 9: 69,282,771 (GRCm39) S430T probably benign Het
Rsph10b T A 5: 143,873,967 (GRCm39) S23T probably damaging Het
Ryr1 T C 7: 28,746,928 (GRCm39) N3773S probably benign Het
Scn4a A G 11: 106,230,180 (GRCm39) Y543H probably damaging Het
Scn4a C A 11: 106,236,373 (GRCm39) G296C probably benign Het
Scn7a T C 2: 66,535,447 (GRCm39) T435A probably benign Het
Shank2 G T 7: 143,964,890 (GRCm39) D833Y probably damaging Het
Slc9a2 T C 1: 40,802,770 (GRCm39) S607P possibly damaging Het
Slx4 G A 16: 3,809,458 (GRCm39) R346W probably damaging Het
Spata20 A T 11: 94,371,340 (GRCm39) C675S probably benign Het
Suclg2 A T 6: 95,563,997 (GRCm39) I196N probably damaging Het
Sv2b G A 7: 74,798,807 (GRCm39) H272Y possibly damaging Het
Taf13 A T 3: 108,488,445 (GRCm39) E109D possibly damaging Het
Tanc2 A G 11: 105,790,606 (GRCm39) T976A probably benign Het
Tax1bp1 A G 6: 52,706,311 (GRCm39) Y104C probably damaging Het
Tfeb T C 17: 48,099,911 (GRCm39) probably null Het
Tlr9 T C 9: 106,101,248 (GRCm39) Y180H probably damaging Het
Trappc9 G A 15: 72,897,816 (GRCm39) R377W probably damaging Het
Ttc12 T A 9: 49,356,499 (GRCm39) T510S probably benign Het
Ubqln1 T C 13: 58,339,895 (GRCm39) E280G probably damaging Het
Urm1 T C 2: 29,731,437 (GRCm39) W44R probably damaging Het
Usp32 A T 11: 84,933,406 (GRCm39) I34N probably benign Het
Vars1 T C 17: 35,233,728 (GRCm39) L1018P probably damaging Het
Vcan A T 13: 89,869,894 (GRCm39) V206D probably damaging Het
Vim T C 2: 13,583,270 (GRCm39) V224A probably damaging Het
Vmn2r106 G T 17: 20,498,997 (GRCm39) H305N probably benign Het
Vmn2r78 A G 7: 86,604,132 (GRCm39) N770S probably damaging Het
Wdr33 T A 18: 32,029,684 (GRCm39) L961Q unknown Het
Xylt2 A G 11: 94,559,575 (GRCm39) S356P possibly damaging Het
Zbtb14 A G 17: 69,694,575 (GRCm39) N91S probably damaging Het
Zc3h6 T C 2: 128,858,654 (GRCm39) L895S probably damaging Het
Zc3h7b C T 15: 81,661,289 (GRCm39) P376L probably benign Het
Zfp131 T C 13: 120,228,079 (GRCm39) T523A 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
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
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'- GCATTGCCCACTAACTCAAAGCCTG -3'
(R):5'- AAGAAGCCAAGCCCGAAGTGTGTC -3'

Sequencing Primer
(F):5'- AAGCCCTTGTACGTGGATGATAC -3'
(R):5'- AAGTGTGTCCCCACCAAGTG -3'
Posted On 2014-05-14