Incidental Mutation 'IGL00434:Ighv1-85'
ID 332414
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ighv1-85
Ensembl Gene ENSMUSG00000096150
Gene Name immunoglobulin heavy variable 1-85
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00434
Quality Score
Status
Chromosome 12
Chromosomal Location 115963648-115963941 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 115963654 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Tryptophan at position 115 (C115W)
Ref Sequence ENSEMBL: ENSMUSP00000100333 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103552]
AlphaFold A0A075B5Y6
Predicted Effect probably damaging
Transcript: ENSMUST00000103552
AA Change: C115W

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000100333
Gene: ENSMUSG00000096150
AA Change: C115W

DomainStartEndE-ValueType
IGv 36 117 9.15e-30 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arid2 T C 15: 96,269,181 (GRCm39) V1098A probably damaging Het
Bltp1 T C 3: 37,041,448 (GRCm39) F2609L probably damaging Het
Ccdc126 C T 6: 49,311,239 (GRCm39) probably benign Het
Cds2 T C 2: 132,135,271 (GRCm39) L54P probably damaging Het
Cdsn A T 17: 35,865,740 (GRCm39) S90C unknown Het
Clcn6 G T 4: 148,098,195 (GRCm39) D581E probably damaging Het
Clec4f T A 6: 83,630,198 (GRCm39) H120L possibly damaging Het
Col12a1 T C 9: 79,560,614 (GRCm39) T1838A probably benign Het
Col22a1 T C 15: 71,878,524 (GRCm39) D211G possibly damaging Het
Cpne8 T C 15: 90,381,261 (GRCm39) probably benign Het
Dgkk T A X: 6,772,697 (GRCm39) M462K probably benign Het
Dhx29 T A 13: 113,091,759 (GRCm39) H834Q probably benign Het
Esyt1 A G 10: 128,353,504 (GRCm39) Y578H possibly damaging Het
Fnip2 C A 3: 79,419,796 (GRCm39) probably benign Het
Fut1 T G 7: 45,268,855 (GRCm39) C270G probably damaging Het
Ganab T A 19: 8,884,707 (GRCm39) V170D probably damaging Het
Gys1 T A 7: 45,094,256 (GRCm39) M364K possibly damaging Het
Igkv4-74 T G 6: 69,162,044 (GRCm39) T42P probably damaging Het
Jmjd4 A G 11: 59,341,321 (GRCm39) Y84C probably damaging Het
Kif11 A C 19: 37,399,857 (GRCm39) E781D possibly damaging Het
Kif14 G A 1: 136,396,756 (GRCm39) S354N probably benign Het
Klf1 C T 8: 85,628,628 (GRCm39) P9S possibly damaging Het
Lrrn3 T C 12: 41,502,191 (GRCm39) probably benign Het
Ltbp4 C A 7: 27,028,230 (GRCm39) R309L probably damaging Het
Marchf10 T C 11: 105,293,014 (GRCm39) E131G possibly damaging Het
Men1 G A 19: 6,387,237 (GRCm39) probably null Het
Mgme1 T A 2: 144,121,056 (GRCm39) probably benign Het
Nkiras2 G A 11: 100,515,808 (GRCm39) G45D probably damaging Het
Orc2 A T 1: 58,532,875 (GRCm39) D16E possibly damaging Het
Pcyox1l T C 18: 61,830,613 (GRCm39) T420A probably benign Het
Pira13 C A 7: 3,826,088 (GRCm39) G302C probably damaging Het
Pm20d1 A G 1: 131,741,738 (GRCm39) probably benign Het
Ppp1r3c T C 19: 36,711,503 (GRCm39) D89G probably damaging Het
Ppp2ca G A 11: 52,012,776 (GRCm39) R302H probably benign Het
Riok3 T C 18: 12,281,904 (GRCm39) V291A probably damaging Het
Rragd A G 4: 33,007,219 (GRCm39) probably benign Het
Scai C A 2: 38,998,406 (GRCm39) L174F probably damaging Het
Slc25a44 T C 3: 88,323,369 (GRCm39) I227V probably benign Het
Slc35f1 T C 10: 52,938,548 (GRCm39) L160P probably damaging Het
Slc38a1 A G 15: 96,483,504 (GRCm39) Y275H possibly damaging Het
Slco6b1 A G 1: 96,916,375 (GRCm39) noncoding transcript Het
Spag8 G T 4: 43,652,890 (GRCm39) C190* probably null Het
Tbr1 T C 2: 61,635,625 (GRCm39) F192L probably benign Het
Tti1 C T 2: 157,850,886 (GRCm39) E118K probably damaging Het
Tti1 T A 2: 157,850,885 (GRCm39) E118V probably damaging Het
Vcan G T 13: 89,852,821 (GRCm39) P713Q probably damaging Het
Vcf2 A T X: 149,181,395 (GRCm39) V132E possibly damaging Het
Wt1 G T 2: 104,974,486 (GRCm39) probably null Het
Xylt1 T A 7: 117,249,912 (GRCm39) I694N probably damaging Het
Zfp516 T A 18: 82,975,233 (GRCm39) M477K probably benign Het
Other mutations in Ighv1-85
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01389:Ighv1-85 APN 12 115,963,671 (GRCm39) missense probably damaging 1.00
R3008:Ighv1-85 UTSW 12 115,963,704 (GRCm39) missense probably damaging 0.97
R3707:Ighv1-85 UTSW 12 115,963,836 (GRCm39) missense probably damaging 1.00
R3708:Ighv1-85 UTSW 12 115,963,836 (GRCm39) missense probably damaging 1.00
R5542:Ighv1-85 UTSW 12 115,963,847 (GRCm39) missense probably benign 0.02
R5644:Ighv1-85 UTSW 12 115,963,680 (GRCm39) missense possibly damaging 0.89
R7311:Ighv1-85 UTSW 12 115,963,799 (GRCm39) missense probably damaging 0.99
R7846:Ighv1-85 UTSW 12 115,963,937 (GRCm39) missense possibly damaging 0.63
R8186:Ighv1-85 UTSW 12 115,963,923 (GRCm39) missense probably benign 0.13
R8249:Ighv1-85 UTSW 12 115,963,844 (GRCm39) missense probably benign
R9570:Ighv1-85 UTSW 12 115,963,794 (GRCm39) missense probably benign
Posted On 2015-08-05