Incidental Mutation 'IGL01541:Igkv6-32'
ID 90169
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: 0.082) question?
Stock # IGL01541
Quality Score
Status
Chromosome 6
Chromosomal Location 70051008-70051568 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 70051290 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 22 (I22T)
Ref Sequence ENSEMBL: ENSMUSP00000100178 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103377]
AlphaFold A0A140T8N9
Predicted Effect probably benign
Transcript: ENSMUST00000103377
AA Change: I22T

PolyPhen 2 Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000100178
Gene: ENSMUSG00000076576
AA Change: I22T

DomainStartEndE-ValueType
IGv 38 110 9.68e-20 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb5 G A 12: 118,875,169 (GRCm39) H668Y probably benign Het
Adamts10 A G 17: 33,762,205 (GRCm39) S505G probably benign Het
Ahnak C T 19: 8,985,243 (GRCm39) H2176Y possibly damaging Het
Ash1l G T 3: 88,973,572 (GRCm39) D2544Y probably damaging Het
Ccdc88a T A 11: 29,350,283 (GRCm39) F88L probably benign Het
Cdc42bpa A T 1: 179,978,723 (GRCm39) probably null Het
Celsr3 T C 9: 108,708,907 (GRCm39) V1251A probably damaging Het
CN725425 T A 15: 91,129,955 (GRCm39) F273I possibly damaging Het
Eif2b1 A G 5: 124,714,965 (GRCm39) C104R probably damaging Het
Ercc3 A T 18: 32,381,372 (GRCm39) D396V possibly damaging Het
Fga A T 3: 82,940,014 (GRCm39) D556V probably damaging Het
Frg1 C T 8: 41,863,362 (GRCm39) probably benign Het
Fto T C 8: 92,136,376 (GRCm39) Y217H probably damaging Het
Garin4 A T 1: 190,896,606 (GRCm39) Y12* probably null Het
Grin3a A T 4: 49,792,533 (GRCm39) V400E probably damaging Het
Gtse1 T A 15: 85,759,855 (GRCm39) L682* probably null Het
Lama1 G A 17: 68,092,065 (GRCm39) R1646H probably benign Het
Lamp1 T C 8: 13,215,905 (GRCm39) C35R probably damaging Het
Lzts3 A T 2: 130,478,126 (GRCm39) L324Q probably damaging Het
Muc6 T A 7: 141,236,069 (GRCm39) R453* probably null Het
Naa35 T A 13: 59,748,777 (GRCm39) H132Q probably damaging Het
Pgm5 C A 19: 24,793,777 (GRCm39) G296W probably damaging Het
Pkd1 T A 17: 24,805,272 (GRCm39) C3275S probably damaging Het
Podxl2 A G 6: 88,826,331 (GRCm39) L325P probably benign Het
Prom2 A G 2: 127,371,050 (GRCm39) probably null Het
Rab12 T C 17: 66,804,404 (GRCm39) S185G probably damaging Het
Rnf43 T G 11: 87,621,046 (GRCm39) M313R probably null Het
Rusc2 T C 4: 43,415,840 (GRCm39) V382A probably benign Het
Sbno1 A T 5: 124,516,618 (GRCm39) probably benign Het
Smg6 T C 11: 74,816,770 (GRCm39) I10T probably benign Het
Smpd1 T C 7: 105,205,033 (GRCm39) F304S possibly damaging Het
Spta1 G A 1: 174,044,725 (GRCm39) V1454I probably benign Het
Tdrd7 A T 4: 46,018,551 (GRCm39) I722F possibly damaging Het
Topors T C 4: 40,262,364 (GRCm39) T307A possibly damaging Het
Ttn C T 2: 76,807,502 (GRCm39) R77Q probably damaging Het
Vmn1r210 C T 13: 23,011,778 (GRCm39) M169I probably benign Het
Zc3h4 A G 7: 16,168,257 (GRCm39) S789G unknown Het
Zfp629 G T 7: 127,211,917 (GRCm39) probably benign Het
Zfp977 C A 7: 42,230,156 (GRCm39) R123I probably benign Het
Other mutations in Igkv6-32
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03183:Igkv6-32 APN 6 70,051,556 (GRCm39) missense probably benign 0.01
IGL03196:Igkv6-32 APN 6 70,051,042 (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 2013-12-03