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30058 Timm8a1

30058

Timm8a1

translocase of inner mitochondrial membrane 8A1

protein-coding

Mus musculus

基因描述

Type Description
Definition translocase of inner mitochondrial membrane 8A1

研究结论

Date Results Publications
2010-01-21 00:00:00 Human deafness dystonia syndrome is caused by a defect in assembly of this protein complex. The defect is caused by a point mutation (a missense mutation). 11875042

名称对应

Type IDs
Synonymous DXHXS1274E, Ddp1, Fci-12, Tim8a, Timm8a
Gene
UniProtKB-ID: TIM8A_MOUSE
UniprotKB: Q9WVA2
UniParc: UPI0000001875
EMBL: BC004796, AK090079, AF150081, AK165573, AK011402, AB031055, BC094631, AK088903
Ensembl: ENSMUSG00000048007
KO: mmu:30058
Nucleutide sequences
EMBL-CDS: BAC40644.1, BAB27594.1, BAC41082.1, AAH94631.1, BAA90770.1, AAH04796.1, AAD39988.1, BAE38265.1
Ensembl_TRS: ENSMUST00000054213
Protein sequencees
Ensembl_PRO: ENSMUSP00000050156
RefSeq: NP_038926.1
Others
UniRef100: UniRef100_Q9WVA2
UniRef90: UniRef90_Q9WVA2
UniRef50: UniRef50_Q9WVA1
UniGene: Mm.214504
CCDS: CCDS41122.1

全选

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