KEGG   Homo sapiens (human): 23787
Entry
23787             CDS       T01001                                 
Symbol
MTCH1, CGI-64, PIG60, PSAP, SLC25A49
Name
(RefSeq) mitochondrial carrier 1
  KO
K17885  mitochondrial carrier
Organism
hsa  Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    23787 (MTCH1)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    23787 (MTCH1)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial quality control factors
  Mitochondrial dynamics
   Fission and Fusion factors
    23787 (MTCH1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   23787 (MTCH1)
SSDB
Motif
Pfam: Mito_carr DUF7265
Other DBs
NCBI-GeneID: 23787
NCBI-ProteinID: NP_001258570
OMIM: 610449
HGNC: 17586
Ensembl: ENSG00000137409
UniProt: Q9NZJ7 A8YXX5
Position
6:complement(36968135..36986551)
AA seq 389 aa
MGASDPEVAPWARGGAAGMAGAGAGAGARGGAAAGVEARARDPPPAHRAHPRHPRPAAQP
SARRMDGGSGGLGSGDNAPTTEALFVALGAGVTALSHPLLYVKLLIQVGHEPMPPTLGTN
VLGRKVLYLPSFFTYAKYIVQVDGKIGLFRGLSPRLMSNALSTVTRGSMKKVFPPDEIEQ
VSNKDDMKTSLKKVVKETSYEMMMQCVSRMLAHPLHVISMRCMVQFVGREAKYSGVLSSI
GKIFKEEGLLGFFVGLIPHLLGDVVFLWGCNLLAHFINAYLVDDSVSDTPGGLGNDQNPG
SQFSQALAIRSYTKFVMGIAVSMLTYPFLLVGDLMAVNNCGLQAGLPPYSPVFKSWIHCW
KYLSVQGQLFRGSSLLFRRVSSGSCFALE
NT seq 1170 nt   +upstreamnt  +downstreamnt
atgggagcttcggacccggaagtggcgccctgggctcgcggcggtgccgcggggatggcg
ggagccggagctggagccggagctcgcggcggagcggcggcgggggtcgaggctcgagct
cgcgatccaccgcccgcgcaccgcgcacatcctcgccaccctcggcctgcggctcagccc
tcggcccgcaggatggatggcgggtcagggggcctggggtctggggacaacgccccgacc
actgaggctcttttcgtggcactgggcgcgggcgtgacggcgctcagccatcccctgctc
tacgtgaagctgctcatccaggtgggtcatgagccgatgccccccacccttgggaccaat
gtgctggggaggaaggtcctctatctgccgagcttcttcacctacgccaagtacatcgtg
caagtggatggtaagatagggctgttccgaggcctgagtccccggctgatgtccaacgcc
ctctctactgtgactcggggtagcatgaagaaggttttccctccagatgagattgagcag
gtttccaacaaggatgatatgaagacttccctgaagaaagttgtgaaggagacctcctac
gagatgatgatgcagtgtgtgtcccgcatgttggcccaccccctgcatgtcatctcaatg
cgctgcatggtccagtttgtgggacgggaggccaagtacagtggtgtgctgagctccatt
gggaagattttcaaagaggaagggctgctgggattcttcgttggattaatccctcacctc
ctgggcgatgtggttttcttgtggggctgtaacctgctggcccacttcatcaatgcctac
ctggtggatgacagcgtgagtgacaccccaggggggctgggaaacgaccagaatccaggt
tcccagttcagccaggccctggccatccggagctataccaagttcgtgatggggattgca
gtgagcatgctgacctaccccttcctgctagttggcgacctcatggctgtgaacaactgc
gggctgcaagctgggctccccccttactccccagtgttcaaatcctggattcactgctgg
aagtacctgagtgtgcagggccagctcttccgaggctccagcctgcttttccgccgggtg
tcatcaggatcatgctttgccctggagtaa

  All links  
Disease (1)   
   OMIM (1)   
Gene (37)   
   RefGene (13)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (19)   
   OC (1)   
Protein sequence (7)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (49)   
   RefSeq(nuc) (5)   
   GenBank (22)   
   EMBL (22)   
Protein domain (2)   
   Pfam (2)   
All databases (96)   

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