Incidental Mutation 'IGL02274:Igkv13-55-1'
ID 287296
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Igkv13-55-1
Ensembl Gene ENSMUSG00000106213
Gene Name immunoglobulin kappa chain variable 13-55-1
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02274
Quality Score
Status
Chromosome 6
Chromosomal Location 69576870-69577246 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to G at 69577132 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: ENSMUST00000200400
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgef10 A G 8: 14,997,205 (GRCm39) D48G probably damaging Het
Asnsd1 T C 1: 53,386,734 (GRCm39) I298V probably benign Het
Cacna2d3 G T 14: 28,678,827 (GRCm39) probably null Het
Cbs T C 17: 31,844,922 (GRCm39) probably null Het
Ccm2 C A 11: 6,540,808 (GRCm39) T216K probably damaging Het
Galc C T 12: 98,220,473 (GRCm39) W131* probably null Het
Gemin5 T C 11: 58,047,621 (GRCm39) R318G possibly damaging Het
Gsta3 T G 1: 21,320,012 (GRCm39) V6G possibly damaging Het
Hdlbp A T 1: 93,336,229 (GRCm39) probably null Het
Il17rd A G 14: 26,821,867 (GRCm39) Y387C probably damaging Het
Katnip A G 7: 125,369,742 (GRCm39) probably null Het
Kmt2e C T 5: 23,705,758 (GRCm39) T1344I probably benign Het
L3mbtl4 A C 17: 69,071,579 (GRCm39) H502P probably benign Het
Lrig1 A T 6: 94,640,919 (GRCm39) N95K possibly damaging Het
Neurl2 G T 2: 164,675,012 (GRCm39) R117S probably damaging Het
Nos1 G A 5: 118,035,845 (GRCm39) A449T probably damaging Het
Noxa1 A T 2: 24,975,767 (GRCm39) V435E probably benign Het
Parp9 C T 16: 35,768,317 (GRCm39) R166W probably damaging Het
Pdzd2 A G 15: 12,445,735 (GRCm39) I158T probably damaging Het
Pip5k1c T C 10: 81,142,218 (GRCm39) Y143H probably damaging Het
Qrfpr A G 3: 36,276,285 (GRCm39) V35A probably damaging Het
Rab3gap1 T G 1: 127,866,817 (GRCm39) S881A probably benign Het
Rita1 C T 5: 120,747,858 (GRCm39) A147T probably damaging Het
Scai G A 2: 38,992,329 (GRCm39) probably benign Het
Skic2 T A 17: 35,064,839 (GRCm39) I418F probably damaging Het
Tenm4 A C 7: 96,503,941 (GRCm39) H1300P probably damaging Het
Tmppe A G 9: 114,234,499 (GRCm39) H266R probably benign Het
Wdr11 A T 7: 129,232,896 (GRCm39) probably null Het
Xirp2 A G 2: 67,338,995 (GRCm39) E412G probably benign Het
Zan A G 5: 137,419,429 (GRCm39) V2910A unknown Het
Posted On 2015-04-16