Incidental Mutation 'IGL01738:Igkv14-111'
ID 105778
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Igkv14-111
Ensembl Gene ENSMUSG00000095771
Gene Name immunoglobulin kappa variable 14-111
Synonyms Gm16939
Accession Numbers
Essential gene? Probably non essential (E-score: 0.130) question?
Stock # IGL01738
Quality Score
Status
Chromosome 6
Chromosomal Location 68233388-68233853 bp(+) (GRCm39)
Type of Mutation critical splice donor site
DNA Base Change (assembly) G to A at 68233443 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100121 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000103320]
AlphaFold A0A140T8P9
Predicted Effect probably benign
Transcript: ENSMUST00000103320
SMART Domains Protein: ENSMUSP00000100121
Gene: ENSMUSG00000095771

DomainStartEndE-ValueType
IGv 40 112 4.28e-21 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000158275
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933405L10Rik A T 8: 106,436,668 (GRCm39) D288V probably damaging Het
Agtr1a G A 13: 30,565,021 (GRCm39) V29I probably benign Het
Akap6 G T 12: 52,933,600 (GRCm39) C364F probably damaging Het
Calcrl T G 2: 84,200,793 (GRCm39) M84L probably benign Het
Cep128 C A 12: 91,197,616 (GRCm39) G402C probably damaging Het
Cfap43 A G 19: 47,785,624 (GRCm39) L422P probably damaging Het
Cnbd2 C A 2: 156,217,537 (GRCm39) probably benign Het
Col27a1 A G 4: 63,182,016 (GRCm39) probably benign Het
Cyp3a44 A G 5: 145,731,745 (GRCm39) S134P probably damaging Het
Dync2h1 A C 9: 7,114,922 (GRCm39) L179R possibly damaging Het
Ell T A 8: 71,034,331 (GRCm39) probably benign Het
Gfm1 A G 3: 67,363,994 (GRCm39) E490G probably benign Het
Glt1d1 T G 5: 127,709,419 (GRCm39) probably benign Het
Gm10267 A T 18: 44,292,342 (GRCm39) I10K possibly damaging Het
Htra4 A G 8: 25,515,727 (GRCm39) V437A probably damaging Het
Ighv1-69 T C 12: 115,587,061 (GRCm39) Q24R possibly damaging Het
Ipcef1 A T 10: 6,840,575 (GRCm39) I374N probably damaging Het
Iqgap1 T C 7: 80,373,648 (GRCm39) D1447G possibly damaging Het
Mast4 A G 13: 102,873,749 (GRCm39) F1681S probably damaging Het
Mmp3 A T 9: 7,446,946 (GRCm39) N42I possibly damaging Het
Mybpc1 G T 10: 88,406,507 (GRCm39) F126L probably damaging Het
Myo1e A G 9: 70,266,652 (GRCm39) K631E probably damaging Het
Or8b43 A C 9: 38,360,942 (GRCm39) Y258S probably damaging Het
Pcsk5 T A 19: 17,411,144 (GRCm39) probably benign Het
Serpina3b T G 12: 104,097,091 (GRCm39) L124R probably damaging Het
Srgap2 T C 1: 131,224,164 (GRCm39) I95V probably benign Het
Sstr5 A T 17: 25,710,584 (GRCm39) I215N probably damaging Het
Top3b G A 16: 16,698,468 (GRCm39) V104M probably benign Het
Tspan8 G A 10: 115,653,570 (GRCm39) probably null Het
Vmn2r102 A G 17: 19,898,020 (GRCm39) Y345C probably damaging Het
Vmn2r17 G A 5: 109,577,364 (GRCm39) G472S probably damaging Het
Zmpste24 A T 4: 120,918,308 (GRCm39) L438Q probably damaging Het
Other mutations in Igkv14-111
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02752:Igkv14-111 APN 6 68,233,561 (GRCm39) missense probably benign 0.27
R6459:Igkv14-111 UTSW 6 68,233,725 (GRCm39) missense probably benign 0.00
R7328:Igkv14-111 UTSW 6 68,233,709 (GRCm39) missense probably damaging 1.00
Posted On 2014-01-21