Homo sapiens (human): 29928
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Entry
29928 CDS
T01001
Symbol
TIMM22, COXPD43, TEX4, TIM22
Name
(RefSeq) translocase of inner mitochondrial membrane 22
KO
K17790
mitochondrial import inner membrane translocase subunit TIM22
Organism
hsa
Homo sapiens (human)
Disease
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
29928 (TIMM22)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
29928 (TIMM22)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial protein import machinery
Inner mambrane
TIM22 complex
29928 (TIMM22)
Transporters [BR:
hsa02000
]
Other transporters
Primary active transporters [TC:
3
]
29928 (TIMM22)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Tim17
Motif
Other DBs
NCBI-GeneID:
29928
NCBI-ProteinID:
NP_037469
OMIM:
607251
HGNC:
17317
Ensembl:
ENSG00000177370
UniProt:
Q9Y584
Structure
PDB
PDBj
LinkDB
All DBs
Position
17:997129..1003671
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AA seq
194 aa
AA seq
DB search
MAAAAPNAGGSAPETAGSAEAPLQYSLLLQYLVGDKRQPRLLEPGSLGGIPSPAKSEEQK
MIEKAMESCAFKAALACVGGFVLGGAFGVFTAGIDTNVGFDPKDPYRTPTAKEVLKDMGQ
RGMSYAKNFAIVGAMFSCTECLIESYRGTSDWKNSVISGCITGGAIGFRAGLKAGAIGCG
GFAAFSAAIDYYLR
NT seq
585 nt
NT seq
+upstream
nt +downstream
nt
atggcggcggccgcccccaatgccggaggctcggcccctgagacagcgggttccgccgaa
gctccgctgcagtacagcctgctcctgcagtacctggtgggtgacaagcgtcagccccgg
ctcctggagcctgggagcctgggcgggatcccaagtccagccaagagtgaggagcagaag
atgatcgagaaggcgatggaaagctgcgctttcaaggctgcgctggcctgcgtgggagga
tttgtcttaggaggtgcatttggggtgtttaccgctggcatcgataccaacgtgggcttt
gaccctaaggatccttaccgtacaccgactgcaaaagaagtgctgaaagacatggggcag
agaggaatgtcctatgccaaaaatttcgccattgtgggagccatgttttcttgtactgag
tgtttgatagaatcttaccggggaacatcagactggaagaacagtgtcatcagtggctgc
atcacgggaggagctattggtttcagagctggcttaaaggctggggccattggttgtgga
ggttttgctgctttctctgctgcgattgattattacctccggtga
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