Incidental Mutation 'IGL01451:Gm11541'
ID 84629
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11541
Ensembl Gene ENSMUSG00000056008
Gene Name predicted gene 11541
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.133) question?
Stock # IGL01451
Quality Score
Chromosome 11
Chromosomal Location 94694498-94704499 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to G at 94695669 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Alanine at position 84 (D84A)
Ref Sequence ENSEMBL: ENSMUSP00000066721 (fasta)
AlphaFold Q8C4D8
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 On 2013-11-11