Incidental Mutation 'IGL02373:Igkv13-54-1'
ID 291009
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Igkv13-54-1
Ensembl Gene ENSMUSG00000105301
Gene Name immunoglobulin kappa chain variable 13-54-1
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # IGL02373
Quality Score
Status
Chromosome 6
Chromosomal Location 69594032-69594407 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 69594304 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196495
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl1 C T 4: 86,168,042 (GRCm39) L462F probably damaging Het
Adgrv1 T C 13: 81,607,832 (GRCm39) D4080G possibly damaging Het
Apc A C 18: 34,449,212 (GRCm39) D2002A probably damaging Het
Apobr T A 7: 126,184,563 (GRCm39) F25I probably damaging Het
Cyp4a10 T A 4: 115,378,274 (GRCm39) L120* probably null Het
Daam2 A G 17: 49,780,408 (GRCm39) S704P probably damaging Het
Dcst1 G T 3: 89,265,198 (GRCm39) N217K probably damaging Het
Efr3b C T 12: 4,033,391 (GRCm39) V139I probably benign Het
Fmn1 C A 2: 113,194,471 (GRCm39) P57Q unknown Het
Galnt1 G A 18: 24,413,092 (GRCm39) G464D possibly damaging Het
Ggcx T A 6: 72,404,902 (GRCm39) W437R probably damaging Het
Iglon5 T C 7: 43,128,643 (GRCm39) E58G probably benign Het
Met C T 6: 17,491,528 (GRCm39) P97S probably damaging Het
Msantd5f6 T C 4: 73,321,880 (GRCm39) M52V probably benign Het
Myg1 T A 15: 102,245,268 (GRCm39) M158K probably damaging Het
Ncald T A 15: 37,372,453 (GRCm39) M131L probably benign Het
Nipa2 T C 7: 55,582,876 (GRCm39) I290V probably benign Het
Or4f14b C A 2: 111,775,178 (GRCm39) V208L probably benign Het
Or5p79 A T 7: 108,221,310 (GRCm39) Y97F probably benign Het
Or6c219 A G 10: 129,781,334 (GRCm39) L84S probably benign Het
Ppfia3 C T 7: 45,008,273 (GRCm39) R48Q probably damaging Het
Rab12 A G 17: 66,805,060 (GRCm39) L156P probably damaging Het
Slc28a3 C T 13: 58,726,218 (GRCm39) probably null Het
Slc4a11 T C 2: 130,526,818 (GRCm39) N770S probably benign Het
Tanc1 T C 2: 59,626,372 (GRCm39) probably null Het
Vmn2r130 A T 17: 23,295,866 (GRCm39) R679* probably null Het
Vwa5b2 G A 16: 20,423,594 (GRCm39) R1169H probably damaging Het
Other mutations in Igkv13-54-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02944:Igkv13-54-1 APN 6 69,594,374 (GRCm39) exon noncoding transcript
R1832:Igkv13-54-1 UTSW 6 69,594,277 (GRCm39) missense probably benign 0.15
R3080:Igkv13-54-1 UTSW 6 69,594,454 (GRCm39) unclassified probably null
Posted On 2015-04-16