Incidental Mutation 'IGL01451: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 #IGL01451
Quality Score
Chromosomal Location94694498-94704499 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to G at 94695669 bp
Amino Acid Change Aspartic acid to Alanine at position 84 (D84A)
Ref Sequence ENSEMBL: ENSMUSP00000066721 (fasta)
Predicted Effect unknown
Transcript: ENSMUST00000069852
AA Change: D84A
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700003H04Rik A G 3: 124,579,878 S23P possibly damaging Het
Adam1a T C 5: 121,519,376 Y618C probably benign Het
Amigo2 A C 15: 97,245,226 S438R probably benign Het
Atp5k T C 5: 108,434,056 I21V probably benign Het
Dnah2 T C 11: 69,474,191 probably benign Het
Dock2 A G 11: 34,310,390 Y984H probably damaging Het
Dpysl2 T A 14: 66,807,918 I469F possibly damaging Het
Edem3 C T 1: 151,818,628 T886I probably benign Het
Gart T C 16: 91,625,512 T706A probably benign Het
Gfpt2 A T 11: 49,807,690 probably benign Het
Gne T C 4: 44,041,860 probably null Het
Gria4 A T 9: 4,503,652 D321E probably benign Het
Ift122 T G 6: 115,912,604 probably null Het
Lcp2 A T 11: 34,047,345 probably benign Het
Mcm2 C T 6: 88,891,966 probably benign Het
Olfr921 A G 9: 38,775,929 I225V probably benign Het
Ptpru C A 4: 131,769,492 probably benign Het
Rpap2 T C 5: 107,603,626 probably null Het
Slc25a39 T C 11: 102,404,900 T138A probably damaging Het
St6galnac1 A C 11: 116,769,339 S49R probably benign Het
Stat1 T C 1: 52,139,343 L312P probably damaging Het
Tmem198 T C 1: 75,484,370 probably benign Het
Top2a A T 11: 99,011,030 L458Q probably damaging Het
Treml4 T C 17: 48,264,995 probably benign Het
Trpm6 A G 19: 18,809,569 D503G probably damaging Het
Ttn C A 2: 76,945,273 E1854D unknown Het
Ubqln3 A T 7: 104,142,196 M229K possibly damaging Het
Zfyve9 T C 4: 108,682,260 T939A probably damaging Het
Other mutations in Gm11541
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01689:Gm11541 APN 11 94704194 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 On2013-11-11