Incidental Mutation 'IGL03281:Ighv7-1'
ID 415607
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ighv7-1
Ensembl Gene ENSMUSG00000076665
Gene Name immunoglobulin heavy variable 7-1
Synonyms Gm16698
Accession Numbers
Essential gene? Probably non essential (E-score: 0.077) question?
Stock # IGL03281
Quality Score
Status
Chromosome 12
Chromosomal Location 113860028-113860566 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 113860571 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100255 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103474]
AlphaFold A0A075B5S2
Predicted Effect probably benign
Transcript: ENSMUST00000103474
SMART Domains Protein: ENSMUSP00000100255
Gene: ENSMUSG00000076665

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
IGv 36 119 6.1e-35 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810021J22Rik G A 11: 58,771,601 (GRCm39) R361H probably benign Het
Abcd2 G T 15: 91,035,876 (GRCm39) T663K probably damaging Het
Btbd8 A T 5: 107,651,742 (GRCm39) T212S probably benign Het
Bud23 C T 5: 135,092,741 (GRCm39) R28H probably benign Het
Celsr2 T C 3: 108,320,256 (GRCm39) Y852C probably damaging Het
Dll1 C A 17: 15,593,866 (GRCm39) R167L probably benign Het
Hmgxb4 A G 8: 75,750,790 (GRCm39) T538A probably damaging Het
Hrh4 T C 18: 13,155,526 (GRCm39) V355A possibly damaging Het
Hrnr A T 3: 93,230,158 (GRCm39) E132V probably benign Het
Kcnu1 A T 8: 26,382,105 (GRCm39) Q485L probably null Het
Lrp1b T A 2: 40,615,526 (GRCm39) M3626L probably benign Het
Magea6 G T X: 153,707,623 (GRCm39) C144* probably null Het
Map1a G T 2: 121,135,541 (GRCm39) R1881L probably damaging Het
Naip2 T A 13: 100,298,128 (GRCm39) Y636F probably damaging Het
Or12j5 T A 7: 140,083,713 (GRCm39) I220F probably damaging Het
Or6c2 T A 10: 129,362,272 (GRCm39) F59I probably benign Het
Prg4 A G 1: 150,325,839 (GRCm39) probably benign Het
Ptpn4 T G 1: 119,587,642 (GRCm39) Q900H probably damaging Het
Ralgps1 A G 2: 33,062,428 (GRCm39) probably null Het
Rasgrp4 C T 7: 28,845,450 (GRCm39) A381V possibly damaging Het
Selenbp1 A T 3: 94,844,621 (GRCm39) K93* probably null Het
Skint5 T A 4: 113,524,415 (GRCm39) K855N unknown Het
Tssk4 T C 14: 55,887,885 (GRCm39) V27A possibly damaging Het
Ttc39a C A 4: 109,290,219 (GRCm39) Q310K possibly damaging Het
Utp18 C T 11: 93,766,784 (GRCm39) V276I probably damaging Het
Vmn2r45 C A 7: 8,486,603 (GRCm39) L228F probably damaging Het
Other mutations in Ighv7-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01637:Ighv7-1 APN 12 113,860,123 (GRCm39) missense possibly damaging 0.78
IGL03006:Ighv7-1 APN 12 113,860,145 (GRCm39) missense probably damaging 1.00
IGL03051:Ighv7-1 APN 12 113,860,576 (GRCm39) unclassified probably benign
R3008:Ighv7-1 UTSW 12 113,860,071 (GRCm39) missense probably damaging 1.00
R5754:Ighv7-1 UTSW 12 113,860,239 (GRCm39) missense probably damaging 0.99
R6172:Ighv7-1 UTSW 12 113,860,183 (GRCm39) missense probably damaging 0.99
R6213:Ighv7-1 UTSW 12 113,860,141 (GRCm39) missense probably damaging 0.99
R7324:Ighv7-1 UTSW 12 113,860,149 (GRCm39) missense probably damaging 1.00
R8399:Ighv7-1 UTSW 12 113,860,532 (GRCm39) missense unknown
R9193:Ighv7-1 UTSW 12 113,860,110 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02