Incidental Mutation 'IGL01689:Gm11541'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11541
Ensembl Gene ENSMUSG00000056008
Gene Namepredicted gene 11541
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.133) question?
Stock #IGL01689
Quality Score
Chromosomal Location94694498-94704499 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 94704194 bp
Amino Acid Change Valine to Alanine at position 16 (V16A)
Ref Sequence ENSEMBL: ENSMUSP00000066721 (fasta)
Predicted Effect unknown
Transcript: ENSMUST00000069852
AA Change: V16A
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 18 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aox4 A G 1: 58,245,161 probably benign Het
Arhgap10 A G 8: 77,411,134 probably benign Het
Armc9 T C 1: 86,274,418 V766A probably benign Het
Asxl2 A T 12: 3,496,425 Q403L probably benign Het
Cd244 G A 1: 171,582,894 probably benign Het
Cdc34b A G 11: 94,742,519 K182E probably benign Het
Csnk1d A T 11: 120,971,567 F295L probably benign Het
Kdr T C 5: 75,936,840 D1252G probably benign Het
Kif14 A G 1: 136,519,642 D1395G probably damaging Het
Lars T A 18: 42,216,949 Q930L probably benign Het
Lypd5 A G 7: 24,352,629 probably benign Het
Olfr1369-ps1 G A 13: 21,116,073 C127Y probably damaging Het
Paics T C 5: 76,961,291 probably null Het
Pcnt A G 10: 76,411,653 V1015A probably damaging Het
Thada C T 17: 84,446,688 S285N possibly damaging Het
Tlr1 T C 5: 64,925,779 D485G probably damaging Het
Vmn2r66 T C 7: 85,007,825 N124S probably damaging Het
Zfyve26 T C 12: 79,284,053 D464G possibly damaging Het
Other mutations in Gm11541
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01451:Gm11541 APN 11 94695669 missense unknown
R2698:Gm11541 UTSW 11 94695615 nonsense probably null
R4465:Gm11541 UTSW 11 94704222 missense unknown
R5526:Gm11541 UTSW 11 94704118 missense unknown
X0018:Gm11541 UTSW 11 94695625 missense unknown
Posted On2014-01-21