Incidental Mutation 'IGL01705:Igkv4-73'
ID 104550
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Igkv4-73
Ensembl Gene ENSMUSG00000094993
Gene Name immunoglobulin kappa variable 4-73
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.239) question?
Stock # IGL01705
Quality Score
Status
Chromosome 6
Chromosomal Location 69174567-69175100 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to T at 69174709 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold A0N8I8
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199760
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts19 A G 18: 59,166,038 (GRCm39) T1077A possibly damaging Het
Akap13 T C 7: 75,396,515 (GRCm39) V2504A possibly damaging Het
Anks3 A T 16: 4,765,587 (GRCm39) W172R probably benign Het
Asap2 T A 12: 21,299,369 (GRCm39) N633K possibly damaging Het
Astn1 A T 1: 158,331,883 (GRCm39) S326C probably damaging Het
Cachd1 A G 4: 100,840,736 (GRCm39) K900E possibly damaging Het
Cd5 A T 19: 10,703,659 (GRCm39) probably null Het
D130043K22Rik T A 13: 25,041,924 (GRCm39) N284K probably benign Het
Dtna C T 18: 23,678,788 (GRCm39) A38V probably damaging Het
Eny2 C A 15: 44,295,831 (GRCm39) probably null Het
Grm5 A G 7: 87,779,254 (GRCm39) Q930R possibly damaging Het
Lama2 A T 10: 27,065,270 (GRCm39) probably benign Het
Lipg A G 18: 75,081,042 (GRCm39) probably null Het
Neto2 T C 8: 86,367,632 (GRCm39) K371E probably damaging Het
Or8g52 T C 9: 39,630,877 (GRCm39) M118T possibly damaging Het
Paxbp1 A G 16: 90,813,876 (GRCm39) F834L probably benign Het
Paxip1 A T 5: 27,953,857 (GRCm39) S946R probably damaging Het
Pclo A G 5: 14,727,879 (GRCm39) probably benign Het
Plcg2 T C 8: 118,308,401 (GRCm39) L331P probably damaging Het
Reep1 A G 6: 71,750,272 (GRCm39) T95A probably damaging Het
Rfx2 A G 17: 57,092,303 (GRCm39) Y332H possibly damaging Het
Smchd1 A T 17: 71,688,393 (GRCm39) D1288E probably damaging Het
Spag17 A G 3: 99,930,046 (GRCm39) M582V probably benign Het
Susd1 A G 4: 59,332,931 (GRCm39) probably benign Het
Syt9 T G 7: 107,035,559 (GRCm39) L192R probably damaging Het
Tlr6 T C 5: 65,111,473 (GRCm39) K478R probably benign Het
Tmem115 G T 9: 107,412,403 (GRCm39) L242F probably benign Het
Tmt1b T A 10: 128,794,731 (GRCm39) I198F probably benign Het
Tnfaip1 T C 11: 78,416,294 (GRCm39) D263G probably benign Het
Ubqln3 T A 7: 103,791,884 (GRCm39) I69F probably damaging Het
Vps52 T C 17: 34,185,042 (GRCm39) L712P probably damaging Het
Other mutations in Igkv4-73
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4809:Igkv4-73 UTSW 6 69,174,807 (GRCm39) missense unknown
Posted On 2014-01-21