Incidental Mutation 'IGL03366:Ighv8-8'
ID 420080
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ighv8-8
Ensembl Gene ENSMUSG00000104452
Gene Name immunoglobulin heavy variable 8-8
Synonyms Ighv8-8, Gm9740, immunoglobulin heavy variable V8-8
Accession Numbers
Essential gene? Not available question?
Stock # IGL03366
Quality Score
Status
Chromosome 12
Chromosomal Location 115257686-115257982 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 115257760 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 94 (T94S)
Ref Sequence ENSEMBL: ENSMUSP00000142082 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000192591]
AlphaFold A0A0A6YXQ0
Predicted Effect probably benign
Transcript: ENSMUST00000192591
AA Change: T94S

PolyPhen 2 Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000142082
Gene: ENSMUSG00000104452
AA Change: T94S

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
IGv 36 118 7.8e-31 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ap2a2 T A 7: 141,209,186 (GRCm39) S793T probably benign Het
Btnl6 T C 17: 34,727,153 (GRCm39) D459G probably damaging Het
Cacna1g C A 11: 94,347,977 (GRCm39) D704Y probably damaging Het
Cby2 A G 14: 75,820,829 (GRCm39) S299P probably benign Het
Cry2 A G 2: 92,244,060 (GRCm39) I371T probably damaging Het
Dock3 A T 9: 106,882,632 (GRCm39) F384I probably benign Het
Dpp4 T C 2: 62,187,301 (GRCm39) probably null Het
Hecw1 G T 13: 14,552,382 (GRCm39) D72E probably damaging Het
Htt T A 5: 35,064,924 (GRCm39) W3046R probably damaging Het
Hydin A T 8: 110,993,995 (GRCm39) N10Y unknown Het
Igkv4-58 A G 6: 69,477,538 (GRCm39) S20P probably damaging Het
Il4i1 T C 7: 44,486,919 (GRCm39) probably benign Het
Kif13a A T 13: 46,918,099 (GRCm39) S403T probably benign Het
Klhl40 T C 9: 121,612,446 (GRCm39) L616P probably damaging Het
Krt7 T C 15: 101,325,491 (GRCm39) L440P possibly damaging Het
Lpin1 A G 12: 16,594,678 (GRCm39) L755P probably damaging Het
Magee2 C A X: 103,899,134 (GRCm39) E506* probably null Het
Mast3 G A 8: 71,234,207 (GRCm39) R143* probably null Het
Med12 T A X: 100,321,695 (GRCm39) H459Q probably benign Het
Mmp3 T C 9: 7,450,149 (GRCm39) S294P probably benign Het
Muc6 T C 7: 141,234,349 (GRCm39) Y714C probably damaging Het
Myh2 T C 11: 67,074,349 (GRCm39) L662S probably damaging Het
Notch4 G T 17: 34,791,542 (GRCm39) C567F probably damaging Het
Nprl3 A G 11: 32,200,256 (GRCm39) I20T probably damaging Het
Or10ag2 A T 2: 87,248,587 (GRCm39) D65V possibly damaging Het
Pcdhb19 A G 18: 37,631,665 (GRCm39) T487A possibly damaging Het
Phlpp2 A G 8: 110,667,467 (GRCm39) E1332G probably benign Het
Pick1 T C 15: 79,125,481 (GRCm39) S113P probably damaging Het
Ptpru T C 4: 131,507,178 (GRCm39) E1023G probably damaging Het
Rspry1 A C 8: 95,376,962 (GRCm39) I382L probably benign Het
Sf3b3 A C 8: 111,566,586 (GRCm39) V248G probably damaging Het
Smg5 T A 3: 88,253,759 (GRCm39) Y126* probably null Het
Spin1 T C 13: 51,281,973 (GRCm39) V22A probably benign Het
Stab1 C T 14: 30,872,220 (GRCm39) R1189Q possibly damaging Het
Sytl5 A G X: 9,829,939 (GRCm39) D538G probably damaging Het
Taar7e T A 10: 23,913,813 (GRCm39) M101K probably damaging Het
Taf4 A G 2: 179,576,847 (GRCm39) V578A probably damaging Het
Tmem266 G T 9: 55,344,517 (GRCm39) C383F probably benign Het
Trim34a T C 7: 103,910,140 (GRCm39) probably null Het
Vmn2r104 T C 17: 20,249,866 (GRCm39) T802A probably damaging Het
Vmn2r32 A C 7: 7,467,029 (GRCm39) I833S probably damaging Het
Vmn2r85 T C 10: 130,262,328 (GRCm39) D137G probably benign Het
Vps13c C T 9: 67,853,308 (GRCm39) S2467L probably benign Het
Other mutations in Ighv8-8
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4945:Ighv8-8 UTSW 12 115,257,881 (GRCm39) missense probably benign
R7116:Ighv8-8 UTSW 12 115,257,814 (GRCm39) missense probably benign 0.04
Posted On 2016-08-02