Incidental Mutation 'IGL02944:Igkv13-54-1'
ID 364658
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 # IGL02944
Quality Score
Status
Chromosome 6
Chromosomal Location 69594032-69594407 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) C to T at 69594374 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: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akap13 A G 7: 75,258,405 (GRCm39) Q343R probably benign Het
Antxr1 T A 6: 87,165,141 (GRCm39) N432I possibly damaging Het
Arhgap15 T C 2: 44,032,362 (GRCm39) probably null Het
Atp6v1h T A 1: 5,163,578 (GRCm39) probably benign Het
Cav2 T C 6: 17,281,456 (GRCm39) Y33H probably damaging Het
Ccdc175 T A 12: 72,164,667 (GRCm39) D585V probably benign Het
Coro7 T C 16: 4,453,276 (GRCm39) D271G probably benign Het
Cylc1 T A X: 110,167,373 (GRCm39) D551E possibly damaging Het
Dnah1 A T 14: 31,022,828 (GRCm39) I1103N possibly damaging Het
Gmds T A 13: 32,522,435 (GRCm39) Y11F probably benign Het
Irf8 A G 8: 121,481,864 (GRCm39) T318A probably benign Het
Lrrc40 G A 3: 157,747,302 (GRCm39) probably benign Het
Mageb11 A G X: 89,935,868 (GRCm39) K41E probably benign Het
Mbd1 G A 18: 74,410,481 (GRCm39) G428E probably damaging Het
Myom2 A T 8: 15,154,065 (GRCm39) probably null Het
Nav2 C T 7: 49,070,004 (GRCm39) R287W probably damaging Het
Nfs1 C T 2: 155,969,688 (GRCm39) D320N probably damaging Het
Nlrp9a A T 7: 26,258,076 (GRCm39) T565S probably benign Het
Nod1 A T 6: 54,901,932 (GRCm39) I951N possibly damaging Het
Or1n1b T G 2: 36,780,800 (GRCm39) E20A possibly damaging Het
Or2ag1b A G 7: 106,288,476 (GRCm39) L154P probably damaging Het
Or52e8b A G 7: 104,674,130 (GRCm39) L19P probably damaging Het
Or8d2 A T 9: 38,760,048 (GRCm39) I213F possibly damaging Het
Pkhd1l1 T C 15: 44,364,927 (GRCm39) Y689H probably damaging Het
Ppp2r5c A G 12: 110,534,234 (GRCm39) I366V probably benign Het
Ppp3cb T C 14: 20,578,303 (GRCm39) Y149C probably damaging Het
Prdm1 T C 10: 44,317,807 (GRCm39) S354G probably benign Het
Ralgapa1 T A 12: 55,804,736 (GRCm39) Q520L probably benign Het
Slc25a54 A T 3: 108,987,931 (GRCm39) Y24F probably benign Het
Slfn3 T A 11: 83,103,837 (GRCm39) V236E probably damaging Het
Syt6 A G 3: 103,482,865 (GRCm39) probably benign Het
Trim30a G T 7: 104,084,984 (GRCm39) N75K probably benign Het
Vmn1r175 T C 7: 23,508,591 (GRCm39) E12G probably damaging Het
Xylt1 A T 7: 117,233,984 (GRCm39) T504S probably benign Het
Other mutations in Igkv13-54-1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02373:Igkv13-54-1 APN 6 69,594,304 (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 2015-12-18