KEGG   Homo sapiens (human): 1678
Entry
1678              CDS       T01001                                 
Symbol
TIMM8A, DDP, DDP1, DFN1, MTS, TIM8
Name
(RefSeq) translocase of inner mitochondrial membrane 8A
  KO
K17780  mitochondrial import inner membrane translocase subunit TIM8
Organism
hsa  Homo sapiens (human)
Disease
H00989  Mohr-Tranebjaerg syndrome
H01201  Jensen syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    1678 (TIMM8A)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    1678 (TIMM8A)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial protein import machinery
  Inter membrane space
   TIM8/13 complex
    1678 (TIMM8A)
Transporters [BR:hsa02000]
 Other transporters
  Primary active transporters [TC:3]
   1678 (TIMM8A)
SSDB
Motif
Pfam: zf-Tim10_DDP PH_12 XMAP215_CLASP_TOG
Other DBs
NCBI-GeneID: 1678
NCBI-ProteinID: NP_004076
OMIM: 300356
HGNC: 11817
Ensembl: ENSG00000126953
UniProt: O60220
LinkDB
Position
X:complement(101345661..101348742)
AA seq 97 aa
MDSSSSSSAAGLGAVDPQLQHFIEVETQKQRFQQLVHQMTELCWEKCMDKPGPKLDSRAE
ACFVNCVERFIDTSQFILNRLEQTQKSKPVFSESLSD
NT seq 294 nt   +upstreamnt  +downstreamnt
atggattcctcctcctcttcctccgcggcgggtttgggtgcagtggacccgcagttgcag
catttcatcgaggtagagactcaaaagcagcgcttccagcagctggtgcaccagatgact
gaactttgttgggagaagtgcatggacaagcctgggccaaagttggacagtcgggctgag
gcctgttttgtgaactgcgttgagcgcttcattgatacaagccagttcatcttgaatcga
ctggaacagacccagaaatccaagccagttttctcagaaagcctttctgactga

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