Incidental Mutation 'R8354:Igfn1'
ID 660574
Institutional Source Beutler Lab
Gene Symbol Igfn1
Ensembl Gene ENSMUSG00000051985
Gene Name immunoglobulin-like and fibronectin type III domain containing 1
Synonyms 9830123M21Rik
MMRRC Submission 067806-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # R8354 (G1)
Quality Score 225.009
Status Validated
Chromosome 1
Chromosomal Location 135881316-135934080 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 135887619 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Serine at position 2482 (C2482S)
Ref Sequence ENSEMBL: ENSMUSP00000129680 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166193]
AlphaFold no structure available at present
Predicted Effect
SMART Domains Protein: ENSMUSP00000119230
Gene: ENSMUSG00000051985
AA Change: C866S

DomainStartEndE-ValueType
IG 73 159 1.29e-6 SMART
IG_like 258 344 5.45e1 SMART
IG 354 435 1.79e0 SMART
IG 445 524 3.54e-4 SMART
IG 538 624 4.86e-2 SMART
FN3 627 711 3.99e-10 SMART
FN3 727 810 9.1e-14 SMART
FN3 828 911 1.5e-14 SMART
IG 938 1021 6.41e-2 SMART
FN3 1024 1106 3.2e-9 SMART
IGc2 1152 1219 4.89e-7 SMART
Predicted Effect
Predicted Effect possibly damaging
Transcript: ENSMUST00000166193
AA Change: C2482S

PolyPhen 2 Score 0.605 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000129680
Gene: ENSMUSG00000051985
AA Change: C2482S

DomainStartEndE-ValueType
low complexity region 90 101 N/A INTRINSIC
IG 193 279 1.29e-6 SMART
PDB:2LHU|A 302 365 8e-7 PDB
IG_like 378 464 5.45e1 SMART
IG 474 555 1.79e0 SMART
low complexity region 724 739 N/A INTRINSIC
internal_repeat_2 838 1006 9.98e-5 PROSPERO
low complexity region 1067 1084 N/A INTRINSIC
internal_repeat_2 1812 1967 9.98e-5 PROSPERO
Pfam:I-set 2054 2139 6.2e-8 PFAM
IG 2153 2239 4.86e-2 SMART
FN3 2242 2326 3.99e-10 SMART
FN3 2342 2425 9.1e-14 SMART
FN3 2443 2526 1.5e-14 SMART
IG 2553 2636 6.41e-2 SMART
FN3 2639 2721 3.2e-9 SMART
IGc2 2767 2834 4.89e-7 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 99% (70/71)
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd12 A T 2: 150,676,297 (GRCm39) S353R probably damaging Het
Ap1ar T C 3: 127,606,428 (GRCm39) probably null Het
Asxl1 C A 2: 153,235,345 (GRCm39) N213K probably benign Het
Cacna1e A G 1: 154,274,314 (GRCm39) V2197A probably damaging Het
Cacna2d2 G A 9: 107,401,334 (GRCm39) E706K possibly damaging Het
Cfap46 C T 7: 139,233,414 (GRCm39) V296I probably benign Het
Cldn5 A G 16: 18,596,043 (GRCm39) T100A probably benign Het
Ctnna1 C A 18: 35,385,776 (GRCm39) N802K possibly damaging Het
Dennd2b G A 7: 109,124,755 (GRCm39) R675* probably null Het
Dip2c A G 13: 9,671,918 (GRCm39) T968A probably benign Het
Dnaaf5 ACCCAGCACCTGGAGATCGTCC ACC 5: 139,147,614 (GRCm39) probably null Het
Dnah8 A T 17: 30,862,234 (GRCm39) D203V probably benign Het
Dnajc13 A G 9: 104,094,927 (GRCm39) M585T probably damaging Het
Donson G T 16: 91,480,685 (GRCm39) T262K possibly damaging Het
E2f3 T A 13: 30,169,787 (GRCm39) probably benign Het
Fam110c A G 12: 31,125,178 (GRCm39) E380G possibly damaging Het
Gbp9 T G 5: 105,242,027 (GRCm39) T177P probably damaging Het
Gins3 C T 8: 96,364,646 (GRCm39) A132V probably benign Het
Glra3 T A 8: 56,578,345 (GRCm39) Y467* probably null Het
Gm7138 A G 10: 77,612,444 (GRCm39) probably benign Het
Golim4 T C 3: 75,802,308 (GRCm39) E328G probably damaging Het
Habp2 T A 19: 56,301,388 (GRCm39) C270* probably null Het
Hecw2 A G 1: 53,964,467 (GRCm39) probably null Het
Hmcn1 A T 1: 150,634,142 (GRCm39) Y815N possibly damaging Het
Igkv4-71 A G 6: 69,220,260 (GRCm39) V57A probably damaging Het
Itpkb G A 1: 180,160,908 (GRCm39) E345K possibly damaging Het
Itpr3 G A 17: 27,334,893 (GRCm39) V2136M possibly damaging Het
Kcnh3 A G 15: 99,127,211 (GRCm39) T336A probably damaging Het
Kdm4d T C 9: 14,375,235 (GRCm39) T208A possibly damaging Het
Kntc1 T C 5: 123,916,330 (GRCm39) F721S probably damaging Het
Krt10 A G 11: 99,280,086 (GRCm39) probably benign Het
Lgals3bp T A 11: 118,289,367 (GRCm39) N28I probably damaging Het
Matn2 T C 15: 34,378,843 (GRCm39) L293P probably damaging Het
Mical3 T C 6: 120,950,381 (GRCm39) E1010G probably damaging Het
Mpp4 C A 1: 59,169,224 (GRCm39) R380L probably damaging Het
Msh5 A G 17: 35,250,742 (GRCm39) F469L possibly damaging Het
Ncam2 A G 16: 81,309,847 (GRCm39) T446A probably benign Het
Neurl4 A G 11: 69,800,062 (GRCm39) D1050G probably damaging Het
Olfml2b T C 1: 170,509,793 (GRCm39) Y714H possibly damaging Het
Or5d43 T C 2: 88,105,036 (GRCm39) D119G probably damaging Het
Or8c17 T C 9: 38,180,513 (GRCm39) S235P probably benign Het
Pcnx2 T C 8: 126,488,357 (GRCm39) E1729G probably damaging Het
Peg10 GCACATCAGGATCC GCACATCAGGATCCCCATCAGGATCCTCCACATCAGGATCC 6: 4,756,452 (GRCm39) probably benign Het
Pex1 T A 5: 3,681,707 (GRCm39) L1051Q probably damaging Het
Prkag2 T A 5: 25,074,137 (GRCm39) R283* probably null Het
Prrc1 T A 18: 57,504,503 (GRCm39) M238K probably damaging Het
Ptprj T C 2: 90,300,061 (GRCm39) T247A probably benign Het
Ptprz1 A G 6: 22,999,614 (GRCm39) Y568C probably damaging Het
Rab36 G A 10: 74,884,291 (GRCm39) A114T probably damaging Het
Rfx7 T C 9: 72,526,731 (GRCm39) V1307A probably benign Het
Scaf1 A C 7: 44,657,251 (GRCm39) probably benign Het
Sema4g A T 19: 44,986,866 (GRCm39) T440S probably benign Het
Setbp1 A T 18: 78,900,598 (GRCm39) V1023E probably damaging Het
Slc46a2 T C 4: 59,913,931 (GRCm39) I331V possibly damaging Het
Slc4a7 C T 14: 14,786,313 (GRCm38) R1000C probably damaging Het
Sorcs2 T C 5: 36,222,753 (GRCm39) H162R probably benign Het
Spata31f1e T A 4: 42,793,223 (GRCm39) H303L probably benign Het
Strip2 G A 6: 29,920,531 (GRCm39) probably null Het
Stx2 T A 5: 129,071,932 (GRCm39) I42L probably benign Het
Tas2r124 A T 6: 132,732,410 (GRCm39) T240S probably benign Het
Tgfbrap1 A T 1: 43,115,070 (GRCm39) V10D probably damaging Het
Tmem41a T A 16: 21,766,181 (GRCm39) Y19F probably benign Het
Tmprss5 A G 9: 49,018,439 (GRCm39) T74A possibly damaging Het
Trim16 G T 11: 62,727,587 (GRCm39) R216L probably benign Het
Trmt10c T C 16: 55,854,870 (GRCm39) K255R probably benign Het
Trpm2 A T 10: 77,769,483 (GRCm39) V747E probably damaging Het
Ube2v2 T C 16: 15,399,005 (GRCm39) D28G possibly damaging Het
Uty G A Y: 1,157,928 (GRCm39) T705I possibly damaging Het
Vmn2r80 A T 10: 78,984,710 (GRCm39) I21F probably benign Het
Wdr11 T C 7: 129,204,723 (GRCm39) L176S probably damaging Het
Zfp992 A G 4: 146,551,319 (GRCm39) T347A probably benign Het
Other mutations in Igfn1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00753:Igfn1 APN 1 135,894,464 (GRCm39) missense probably damaging 1.00
IGL02299:Igfn1 APN 1 135,881,755 (GRCm39) utr 3 prime probably benign
Bounty UTSW 1 135,904,655 (GRCm39) critical splice donor site probably null
R2276_Igfn1_773 UTSW 1 135,892,479 (GRCm39) missense probably damaging 0.98
R4058_Igfn1_315 UTSW 1 135,897,494 (GRCm39) missense probably benign 0.07
R0144:Igfn1 UTSW 1 135,889,751 (GRCm39) missense probably damaging 0.99
R0190:Igfn1 UTSW 1 135,889,790 (GRCm39) missense probably damaging 1.00
R0350:Igfn1 UTSW 1 135,884,505 (GRCm39) nonsense probably null
R0413:Igfn1 UTSW 1 135,895,334 (GRCm39) missense probably benign 0.23
R0504:Igfn1 UTSW 1 135,896,267 (GRCm39) missense probably benign 0.00
R0606:Igfn1 UTSW 1 135,887,639 (GRCm39) missense probably damaging 1.00
R0681:Igfn1 UTSW 1 135,891,591 (GRCm39) missense possibly damaging 0.88
R0825:Igfn1 UTSW 1 135,890,864 (GRCm39) missense probably damaging 1.00
R0839:Igfn1 UTSW 1 135,882,418 (GRCm39) missense probably damaging 1.00
R1066:Igfn1 UTSW 1 135,898,463 (GRCm39) missense probably benign
R1078:Igfn1 UTSW 1 135,902,585 (GRCm39) missense probably damaging 1.00
R1224:Igfn1 UTSW 1 135,897,494 (GRCm39) missense probably benign 0.07
R1569:Igfn1 UTSW 1 135,896,771 (GRCm39) missense probably benign
R1626:Igfn1 UTSW 1 135,896,705 (GRCm39) missense probably benign 0.29
R1663:Igfn1 UTSW 1 135,896,046 (GRCm39) missense probably benign 0.15
R1677:Igfn1 UTSW 1 135,898,839 (GRCm39) missense probably damaging 0.99
R1709:Igfn1 UTSW 1 135,883,311 (GRCm39) missense probably benign 0.24
R1728:Igfn1 UTSW 1 135,926,421 (GRCm39) missense unknown
R1728:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R1728:Igfn1 UTSW 1 135,910,213 (GRCm39) missense probably benign
R1728:Igfn1 UTSW 1 135,907,653 (GRCm39) missense probably benign 0.00
R1728:Igfn1 UTSW 1 135,899,865 (GRCm39) missense probably benign
R1728:Igfn1 UTSW 1 135,898,149 (GRCm39) missense probably benign
R1728:Igfn1 UTSW 1 135,895,937 (GRCm39) missense probably benign
R1728:Igfn1 UTSW 1 135,887,666 (GRCm39) missense probably damaging 1.00
R1729:Igfn1 UTSW 1 135,910,213 (GRCm39) missense probably benign
R1729:Igfn1 UTSW 1 135,907,653 (GRCm39) missense probably benign 0.00
R1729:Igfn1 UTSW 1 135,899,865 (GRCm39) missense probably benign
R1729:Igfn1 UTSW 1 135,898,149 (GRCm39) missense probably benign
R1729:Igfn1 UTSW 1 135,895,937 (GRCm39) missense probably benign
R1729:Igfn1 UTSW 1 135,887,666 (GRCm39) missense probably damaging 1.00
R1729:Igfn1 UTSW 1 135,926,421 (GRCm39) missense unknown
R1729:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R1730:Igfn1 UTSW 1 135,887,666 (GRCm39) missense probably damaging 1.00
R1730:Igfn1 UTSW 1 135,895,937 (GRCm39) missense probably benign
R1730:Igfn1 UTSW 1 135,898,149 (GRCm39) missense probably benign
R1730:Igfn1 UTSW 1 135,899,865 (GRCm39) missense probably benign
R1730:Igfn1 UTSW 1 135,907,653 (GRCm39) missense probably benign 0.00
R1730:Igfn1 UTSW 1 135,910,213 (GRCm39) missense probably benign
R1730:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R1730:Igfn1 UTSW 1 135,926,421 (GRCm39) missense unknown
R1739:Igfn1 UTSW 1 135,899,865 (GRCm39) missense probably benign
R1739:Igfn1 UTSW 1 135,907,653 (GRCm39) missense probably benign 0.00
R1739:Igfn1 UTSW 1 135,910,213 (GRCm39) missense probably benign
R1739:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R1739:Igfn1 UTSW 1 135,898,149 (GRCm39) missense probably benign
R1739:Igfn1 UTSW 1 135,895,937 (GRCm39) missense probably benign
R1739:Igfn1 UTSW 1 135,887,666 (GRCm39) missense probably damaging 1.00
R1739:Igfn1 UTSW 1 135,926,421 (GRCm39) missense unknown
R1746:Igfn1 UTSW 1 135,897,561 (GRCm39) missense possibly damaging 0.88
R1762:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R1762:Igfn1 UTSW 1 135,910,213 (GRCm39) missense probably benign
R1762:Igfn1 UTSW 1 135,907,653 (GRCm39) missense probably benign 0.00
R1762:Igfn1 UTSW 1 135,899,865 (GRCm39) missense probably benign
R1762:Igfn1 UTSW 1 135,898,149 (GRCm39) missense probably benign
R1762:Igfn1 UTSW 1 135,895,937 (GRCm39) missense probably benign
R1762:Igfn1 UTSW 1 135,887,666 (GRCm39) missense probably damaging 1.00
R1762:Igfn1 UTSW 1 135,926,421 (GRCm39) missense unknown
R1783:Igfn1 UTSW 1 135,910,213 (GRCm39) missense probably benign
R1783:Igfn1 UTSW 1 135,907,653 (GRCm39) missense probably benign 0.00
R1783:Igfn1 UTSW 1 135,899,865 (GRCm39) missense probably benign
R1783:Igfn1 UTSW 1 135,898,149 (GRCm39) missense probably benign
R1783:Igfn1 UTSW 1 135,895,937 (GRCm39) missense probably benign
R1783:Igfn1 UTSW 1 135,887,666 (GRCm39) missense probably damaging 1.00
R1783:Igfn1 UTSW 1 135,926,421 (GRCm39) missense unknown
R1783:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R1784:Igfn1 UTSW 1 135,926,421 (GRCm39) missense unknown
R1784:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R1784:Igfn1 UTSW 1 135,910,213 (GRCm39) missense probably benign
R1784:Igfn1 UTSW 1 135,907,653 (GRCm39) missense probably benign 0.00
R1784:Igfn1 UTSW 1 135,899,865 (GRCm39) missense probably benign
R1784:Igfn1 UTSW 1 135,898,149 (GRCm39) missense probably benign
R1784:Igfn1 UTSW 1 135,895,937 (GRCm39) missense probably benign
R1784:Igfn1 UTSW 1 135,887,666 (GRCm39) missense probably damaging 1.00
R1785:Igfn1 UTSW 1 135,926,421 (GRCm39) missense unknown
R1785:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R1785:Igfn1 UTSW 1 135,910,213 (GRCm39) missense probably benign
R1785:Igfn1 UTSW 1 135,907,653 (GRCm39) missense probably benign 0.00
R1785:Igfn1 UTSW 1 135,899,865 (GRCm39) missense probably benign
R1785:Igfn1 UTSW 1 135,898,149 (GRCm39) missense probably benign
R1785:Igfn1 UTSW 1 135,895,937 (GRCm39) missense probably benign
R1785:Igfn1 UTSW 1 135,887,666 (GRCm39) missense probably damaging 1.00
R1847:Igfn1 UTSW 1 135,897,126 (GRCm39) missense probably benign
R1866:Igfn1 UTSW 1 135,902,606 (GRCm39) splice site probably null
R1921:Igfn1 UTSW 1 135,893,801 (GRCm39) critical splice donor site probably null
R1984:Igfn1 UTSW 1 135,889,782 (GRCm39) missense probably benign 0.39
R2049:Igfn1 UTSW 1 135,902,590 (GRCm39) splice site probably benign
R2049:Igfn1 UTSW 1 135,898,376 (GRCm39) missense probably benign
R2098:Igfn1 UTSW 1 135,906,043 (GRCm39) missense probably damaging 1.00
R2130:Igfn1 UTSW 1 135,902,590 (GRCm39) splice site probably benign
R2141:Igfn1 UTSW 1 135,902,590 (GRCm39) splice site probably benign
R2276:Igfn1 UTSW 1 135,892,479 (GRCm39) missense probably damaging 0.98
R2425:Igfn1 UTSW 1 135,890,840 (GRCm39) missense probably damaging 1.00
R2483:Igfn1 UTSW 1 135,897,275 (GRCm39) missense probably benign
R2504:Igfn1 UTSW 1 135,897,054 (GRCm39) missense probably benign 0.07
R3109:Igfn1 UTSW 1 135,925,586 (GRCm39) missense probably benign 0.12
R3421:Igfn1 UTSW 1 135,904,655 (GRCm39) critical splice donor site probably null
R3423:Igfn1 UTSW 1 135,926,379 (GRCm39) missense probably benign 0.01
R3705:Igfn1 UTSW 1 135,896,147 (GRCm39) missense probably benign
R3871:Igfn1 UTSW 1 135,896,574 (GRCm39) missense probably benign 0.03
R3875:Igfn1 UTSW 1 135,882,352 (GRCm39) missense probably damaging 1.00
R3953:Igfn1 UTSW 1 135,894,918 (GRCm39) missense possibly damaging 0.61
R3955:Igfn1 UTSW 1 135,894,918 (GRCm39) missense possibly damaging 0.61
R3957:Igfn1 UTSW 1 135,894,918 (GRCm39) missense possibly damaging 0.61
R3965:Igfn1 UTSW 1 135,895,557 (GRCm39) missense probably benign
R4006:Igfn1 UTSW 1 135,910,100 (GRCm39) splice site probably null
R4058:Igfn1 UTSW 1 135,897,494 (GRCm39) missense probably benign 0.07
R4059:Igfn1 UTSW 1 135,897,494 (GRCm39) missense probably benign 0.07
R4370:Igfn1 UTSW 1 135,895,844 (GRCm39) missense probably benign 0.00
R4380:Igfn1 UTSW 1 135,895,509 (GRCm39) missense probably benign 0.00
R4495:Igfn1 UTSW 1 135,897,416 (GRCm39) missense possibly damaging 0.79
R4628:Igfn1 UTSW 1 135,887,468 (GRCm39) missense possibly damaging 0.47
R4672:Igfn1 UTSW 1 135,893,107 (GRCm39) missense possibly damaging 0.72
R4682:Igfn1 UTSW 1 135,926,363 (GRCm39) missense probably benign
R4702:Igfn1 UTSW 1 135,894,947 (GRCm39) missense possibly damaging 0.71
R4744:Igfn1 UTSW 1 135,910,196 (GRCm39) missense probably benign 0.07
R4777:Igfn1 UTSW 1 135,882,600 (GRCm39) missense probably benign
R4806:Igfn1 UTSW 1 135,895,095 (GRCm39) missense probably benign 0.01
R4840:Igfn1 UTSW 1 135,895,778 (GRCm39) missense probably benign 0.00
R4894:Igfn1 UTSW 1 135,882,520 (GRCm39) missense probably damaging 1.00
R4998:Igfn1 UTSW 1 135,882,404 (GRCm39) missense probably damaging 1.00
R5092:Igfn1 UTSW 1 135,892,564 (GRCm39) missense probably benign
R5108:Igfn1 UTSW 1 135,910,179 (GRCm39) missense probably benign
R5120:Igfn1 UTSW 1 135,901,240 (GRCm39) missense possibly damaging 0.93
R5127:Igfn1 UTSW 1 135,887,634 (GRCm39) missense probably damaging 1.00
R5231:Igfn1 UTSW 1 135,894,474 (GRCm39) missense probably benign 0.26
R5286:Igfn1 UTSW 1 135,895,599 (GRCm39) missense probably benign 0.10
R5307:Igfn1 UTSW 1 135,892,676 (GRCm39) missense probably damaging 1.00
R5380:Igfn1 UTSW 1 135,893,825 (GRCm39) missense probably damaging 1.00
R5553:Igfn1 UTSW 1 135,895,622 (GRCm39) missense probably damaging 1.00
R5660:Igfn1 UTSW 1 135,898,152 (GRCm39) missense probably benign 0.01
R5779:Igfn1 UTSW 1 135,894,578 (GRCm39) missense probably benign 0.16
R5818:Igfn1 UTSW 1 135,893,864 (GRCm39) missense possibly damaging 0.72
R5832:Igfn1 UTSW 1 135,902,533 (GRCm39) missense probably damaging 0.96
R5933:Igfn1 UTSW 1 135,898,341 (GRCm39) nonsense probably null
R5966:Igfn1 UTSW 1 135,893,152 (GRCm39) missense probably damaging 1.00
R6116:Igfn1 UTSW 1 135,898,205 (GRCm39) missense probably benign 0.00
R6297:Igfn1 UTSW 1 135,892,399 (GRCm39) critical splice donor site probably null
R6652:Igfn1 UTSW 1 135,891,609 (GRCm39) missense probably damaging 1.00
R6737:Igfn1 UTSW 1 135,897,605 (GRCm39) missense probably benign
R6816:Igfn1 UTSW 1 135,887,466 (GRCm39) missense probably benign 0.02
R6886:Igfn1 UTSW 1 135,901,198 (GRCm39) missense probably damaging 1.00
R6888:Igfn1 UTSW 1 135,910,218 (GRCm39) missense probably benign 0.33
R6975:Igfn1 UTSW 1 135,896,183 (GRCm39) missense probably damaging 0.96
R7105:Igfn1 UTSW 1 135,911,956 (GRCm39) missense probably benign 0.11
R7114:Igfn1 UTSW 1 135,894,519 (GRCm39) missense probably benign 0.01
R7233:Igfn1 UTSW 1 135,897,873 (GRCm39) missense probably benign 0.41
R7276:Igfn1 UTSW 1 135,926,376 (GRCm39) missense possibly damaging 0.85
R7354:Igfn1 UTSW 1 135,903,770 (GRCm39) missense possibly damaging 0.72
R7358:Igfn1 UTSW 1 135,891,738 (GRCm39) missense probably damaging 1.00
R7380:Igfn1 UTSW 1 135,889,746 (GRCm39) missense probably damaging 1.00
R7389:Igfn1 UTSW 1 135,894,785 (GRCm39) missense probably benign 0.00
R7513:Igfn1 UTSW 1 135,887,705 (GRCm39) missense probably damaging 1.00
R7718:Igfn1 UTSW 1 135,896,774 (GRCm39) missense probably benign
R7769:Igfn1 UTSW 1 135,910,143 (GRCm39) missense possibly damaging 0.85
R7810:Igfn1 UTSW 1 135,902,527 (GRCm39) missense probably damaging 0.98
R7917:Igfn1 UTSW 1 135,899,706 (GRCm39) missense probably damaging 0.99
R7952:Igfn1 UTSW 1 135,891,693 (GRCm39) missense probably damaging 0.99
R8041:Igfn1 UTSW 1 135,895,797 (GRCm39) nonsense probably null
R8233:Igfn1 UTSW 1 135,895,782 (GRCm39) missense probably benign 0.00
R8363:Igfn1 UTSW 1 135,891,625 (GRCm39) missense probably benign 0.01
R8428:Igfn1 UTSW 1 135,895,520 (GRCm39) missense probably damaging 1.00
R8731:Igfn1 UTSW 1 135,925,574 (GRCm39) missense probably benign 0.02
R8756:Igfn1 UTSW 1 135,895,698 (GRCm39) missense probably benign 0.10
R8797:Igfn1 UTSW 1 135,902,573 (GRCm39) missense possibly damaging 0.93
R8913:Igfn1 UTSW 1 135,891,579 (GRCm39) missense possibly damaging 0.90
R8927:Igfn1 UTSW 1 135,905,984 (GRCm39) missense probably damaging 1.00
R8928:Igfn1 UTSW 1 135,905,984 (GRCm39) missense probably damaging 1.00
R9087:Igfn1 UTSW 1 135,902,606 (GRCm39) splice site probably null
R9109:Igfn1 UTSW 1 135,926,327 (GRCm39) missense probably benign 0.26
R9113:Igfn1 UTSW 1 135,883,328 (GRCm39) missense probably damaging 1.00
R9117:Igfn1 UTSW 1 135,902,528 (GRCm39) missense probably benign 0.03
R9205:Igfn1 UTSW 1 135,903,695 (GRCm39) missense probably damaging 0.96
R9251:Igfn1 UTSW 1 135,894,409 (GRCm39) splice site probably benign
R9260:Igfn1 UTSW 1 135,907,694 (GRCm39) missense probably benign 0.45
R9275:Igfn1 UTSW 1 135,901,185 (GRCm39) missense probably damaging 0.96
R9277:Igfn1 UTSW 1 135,887,520 (GRCm39) missense probably damaging 0.98
R9278:Igfn1 UTSW 1 135,901,185 (GRCm39) missense probably damaging 0.96
R9287:Igfn1 UTSW 1 135,925,544 (GRCm39) missense probably benign 0.33
R9298:Igfn1 UTSW 1 135,926,327 (GRCm39) missense probably benign 0.26
R9356:Igfn1 UTSW 1 135,899,825 (GRCm39) nonsense probably null
R9371:Igfn1 UTSW 1 135,906,001 (GRCm39) missense probably damaging 1.00
R9532:Igfn1 UTSW 1 135,897,229 (GRCm39) missense possibly damaging 0.61
R9653:Igfn1 UTSW 1 135,883,323 (GRCm39) nonsense probably null
R9666:Igfn1 UTSW 1 135,897,692 (GRCm39) missense possibly damaging 0.65
R9741:Igfn1 UTSW 1 135,895,383 (GRCm39) missense probably benign 0.00
R9748:Igfn1 UTSW 1 135,926,336 (GRCm39) missense possibly damaging 0.89
R9796:Igfn1 UTSW 1 135,897,611 (GRCm39) missense probably benign 0.26
Z1176:Igfn1 UTSW 1 135,899,738 (GRCm39) missense probably damaging 0.99
Z1177:Igfn1 UTSW 1 135,897,305 (GRCm39) missense probably benign 0.26
Z1177:Igfn1 UTSW 1 135,883,547 (GRCm39) missense probably damaging 1.00
Z1177:Igfn1 UTSW 1 135,910,164 (GRCm39) missense possibly damaging 0.73
Predicted Primers PCR Primer
(F):5'- CGGCATGGCATGAACCAATG -3'
(R):5'- AGTTCTGCAGAAACCCCTAAG -3'

Sequencing Primer
(F):5'- TGGCATGAACCAATGTGTCC -3'
(R):5'- CAAGACTCCTTGGTTGGAAGACTC -3'
Posted On 2021-01-18