Incidental Mutation 'IGL02004:Igkv10-94'
ID 182203
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Igkv10-94
Ensembl Gene ENSMUSG00000096490
Gene Name immunoglobulin kappa variable 10-94
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.264) question?
Stock # IGL02004
Quality Score
Status
Chromosome 6
Chromosomal Location 68681492-68681962 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 68681928 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Stop codon at position 12 (L12*)
Ref Sequence ENSEMBL: ENSMUSP00000100131 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103330]
AlphaFold A0A075B5L1
Predicted Effect probably null
Transcript: ENSMUST00000103330
AA Change: L12*
SMART Domains Protein: ENSMUSP00000100131
Gene: ENSMUSG00000096490
AA Change: L12*

DomainStartEndE-ValueType
low complexity region 8 13 N/A INTRINSIC
IGv 38 110 2.11e-20 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427D14Rik G T 11: 72,082,423 (GRCm39) A301E possibly damaging Het
C4b A T 17: 34,957,984 (GRCm39) probably benign Het
Cep85 A G 4: 133,894,698 (GRCm39) V36A probably damaging Het
Cnot10 A T 9: 114,451,998 (GRCm39) F259L probably damaging Het
Crim1 T C 17: 78,680,004 (GRCm39) probably benign Het
Crispld1 G A 1: 17,817,744 (GRCm39) A216T probably damaging Het
Cyp8b1 T C 9: 121,744,058 (GRCm39) I425V probably benign Het
Fat2 A T 11: 55,173,666 (GRCm39) V2349D probably damaging Het
Fer G T 17: 64,231,174 (GRCm39) probably null Het
Galnt3 T C 2: 65,926,270 (GRCm39) T313A probably damaging Het
Hsd3b9 T A 3: 98,363,735 (GRCm39) R37W probably damaging Het
Kcnj3 G A 2: 55,327,243 (GRCm39) D11N probably benign Het
Kit T A 5: 75,781,674 (GRCm39) S368T probably benign Het
Mark1 G A 1: 184,644,786 (GRCm39) S390L possibly damaging Het
Mpped1 C A 15: 83,684,357 (GRCm39) S126R probably damaging Het
Myh15 A C 16: 48,930,892 (GRCm39) probably benign Het
Nat1 G A 8: 67,943,878 (GRCm39) E85K probably benign Het
Or9q1 T C 19: 13,805,427 (GRCm39) D111G possibly damaging Het
Pde3b A T 7: 114,118,852 (GRCm39) M664L possibly damaging Het
Phrf1 A G 7: 140,840,246 (GRCm39) D1147G probably benign Het
Pth1r G T 9: 110,571,376 (GRCm39) probably benign Het
Shank3 C T 15: 89,387,502 (GRCm39) probably benign Het
Slc39a7 A C 17: 34,250,095 (GRCm39) probably benign Het
Slc6a1 A G 6: 114,291,286 (GRCm39) T520A probably benign Het
St3gal2 C A 8: 111,696,804 (GRCm39) A317E probably damaging Het
St3gal3 C A 4: 117,817,236 (GRCm39) L139F possibly damaging Het
Sval3 T A 6: 41,949,776 (GRCm39) probably benign Het
Syvn1 G A 19: 6,102,437 (GRCm39) A502T probably benign Het
Tm4sf1 T C 3: 57,200,499 (GRCm39) I68V possibly damaging Het
Tnrc6a T A 7: 122,780,589 (GRCm39) N1326K possibly damaging Het
Tvp23b G A 11: 62,782,826 (GRCm39) C174Y probably damaging Het
Zfp750 T C 11: 121,402,975 (GRCm39) D591G probably benign Het
Other mutations in Igkv10-94
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1299:Igkv10-94 UTSW 6 68,681,482 (GRCm39) unclassified probably benign
R2433:Igkv10-94 UTSW 6 68,681,559 (GRCm39) missense probably benign 0.29
R5122:Igkv10-94 UTSW 6 68,681,655 (GRCm39) nonsense probably null
R5292:Igkv10-94 UTSW 6 68,681,582 (GRCm39) missense probably damaging 0.99
R6540:Igkv10-94 UTSW 6 68,681,507 (GRCm39) missense probably benign 0.00
R7135:Igkv10-94 UTSW 6 68,681,727 (GRCm39) missense possibly damaging 0.70
R7872:Igkv10-94 UTSW 6 68,681,913 (GRCm39) critical splice donor site probably benign
R7965:Igkv10-94 UTSW 6 68,681,595 (GRCm39) missense probably damaging 1.00
R8558:Igkv10-94 UTSW 6 68,681,636 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07