Incidental Mutation 'IGL03196:Igkv6-32'
ID 412805
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Igkv6-32
Ensembl Gene ENSMUSG00000076576
Gene Name immunoglobulin kappa variable 6-32
Synonyms ENSMUSG00000053690
Accession Numbers
Essential gene? Probably non essential (E-score: 0.095) question?
Stock # IGL03196
Quality Score
Status
Chromosome 6
Chromosomal Location 70051008-70051568 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 70051042 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 105 (V105I)
Ref Sequence ENSEMBL: ENSMUSP00000100178 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103377]
AlphaFold A0A140T8N9
Predicted Effect probably benign
Transcript: ENSMUST00000103377
AA Change: V105I

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000100178
Gene: ENSMUSG00000076576
AA Change: V105I

DomainStartEndE-ValueType
IGv 38 110 9.68e-20 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700003E16Rik T C 6: 83,138,045 (GRCm39) V57A probably damaging Het
Adck1 T C 12: 88,397,885 (GRCm39) V173A probably damaging Het
Adgrv1 C A 13: 81,594,597 (GRCm39) R4139L probably benign Het
Aqp4 T G 18: 15,526,566 (GRCm39) D305A probably benign Het
Cadm1 T C 9: 47,710,675 (GRCm39) S193P possibly damaging Het
Ccdc88a T C 11: 29,432,340 (GRCm39) S377P possibly damaging Het
Clic5 C A 17: 44,552,960 (GRCm39) H71Q possibly damaging Het
Col20a1 G A 2: 180,649,671 (GRCm39) probably null Het
Col5a1 A G 2: 27,865,610 (GRCm39) D759G unknown Het
Cplane1 A T 15: 8,230,826 (GRCm39) K1034N probably damaging Het
Cpt1b A G 15: 89,308,598 (GRCm39) V110A probably benign Het
Cts8 C T 13: 61,401,272 (GRCm39) G85S probably benign Het
Cul5 T A 9: 53,537,180 (GRCm39) M551L probably damaging Het
Eno1b T A 18: 48,180,558 (GRCm39) D245E probably damaging Het
Fgf1 A T 18: 38,975,028 (GRCm39) Y140* probably null Het
Flt1 A G 5: 147,551,937 (GRCm39) probably null Het
Fndc7 A G 3: 108,790,760 (GRCm39) Y89H probably damaging Het
Gm3127 A T 14: 15,432,259 (GRCm39) M254L probably benign Het
Gm5849 T C 3: 90,685,089 (GRCm39) E32G probably damaging Het
Gys1 T C 7: 45,104,241 (GRCm39) probably benign Het
H2ap A G X: 9,713,349 (GRCm39) Q27R possibly damaging Het
Hdgfl2 T C 17: 56,400,607 (GRCm39) V125A probably benign Het
Lmo3 T C 6: 138,342,993 (GRCm39) T140A probably benign Het
Marf1 A G 16: 13,958,123 (GRCm39) V793A possibly damaging Het
Mep1b A C 18: 21,228,121 (GRCm39) I575L probably benign Het
Mtmr4 T A 11: 87,491,609 (GRCm39) I155N possibly damaging Het
Muc2 T C 7: 141,301,367 (GRCm39) F361L probably damaging Het
Ncoa7 T A 10: 30,523,510 (GRCm39) probably benign Het
Nme6 C T 9: 109,670,561 (GRCm39) R71W probably damaging Het
Or56b1b T C 7: 108,164,061 (GRCm39) S314G probably benign Het
Or9g4b G A 2: 85,616,365 (GRCm39) G170D possibly damaging Het
Or9m2 A T 2: 87,820,826 (GRCm39) I124F possibly damaging Het
Osbpl9 C T 4: 108,930,061 (GRCm39) V357I probably damaging Het
Ppp4r3a A G 12: 101,015,913 (GRCm39) probably benign Het
Rnf216 T C 5: 143,066,766 (GRCm39) R474G probably damaging Het
Rpp25l A G 4: 41,712,541 (GRCm39) V78A possibly damaging Het
Sh3bp2 C A 5: 34,714,687 (GRCm39) P245Q probably damaging Het
Slc33a1 A G 3: 63,871,151 (GRCm39) F154S possibly damaging Het
Wasf2 T A 4: 132,921,732 (GRCm39) S284T unknown Het
Wdtc1 T C 4: 133,022,648 (GRCm39) E566G probably damaging Het
Zcchc14 C T 8: 122,335,877 (GRCm39) probably benign Het
Other mutations in Igkv6-32
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01541:Igkv6-32 APN 6 70,051,290 (GRCm39) missense probably benign 0.01
IGL03183:Igkv6-32 APN 6 70,051,556 (GRCm39) missense probably benign 0.01
R5068:Igkv6-32 UTSW 6 70,051,267 (GRCm39) missense possibly damaging 0.69
R5223:Igkv6-32 UTSW 6 70,051,207 (GRCm39) missense probably benign 0.00
R6425:Igkv6-32 UTSW 6 70,051,284 (GRCm39) missense probably damaging 0.99
R7664:Igkv6-32 UTSW 6 70,051,282 (GRCm39) missense probably damaging 1.00
R8070:Igkv6-32 UTSW 6 70,051,089 (GRCm39) missense probably damaging 1.00
R8093:Igkv6-32 UTSW 6 70,051,547 (GRCm39) missense probably benign 0.30
R8679:Igkv6-32 UTSW 6 70,051,063 (GRCm39) missense possibly damaging 0.65
Z1176:Igkv6-32 UTSW 6 70,051,570 (GRCm39) start gained probably benign
Posted On 2016-08-02