KEGG   Homo sapiens (human): 51660
Entry
51660             CDS       T01001                                 
Symbol
MPC1, BRP44L, CGI-129, MPYCD, SLC54A1
Name
(RefSeq) mitochondrial pyruvate carrier 1
  KO
K22138  mitochondrial pyruvate carrier 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa05415  Diabetic cardiomyopathy
Disease
H02197  Mitochondrial pyruvate carrier deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    51660 (MPC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    51660 (MPC1)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    51660 (MPC1)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial protein import machinery
  Inner mambrane
   Other inner membrane factors
    51660 (MPC1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC54: Mitochondrial pyruvate carrier
   51660 (MPC1)
SSDB
Motif
Pfam: MPC
Other DBs
NCBI-GeneID: 51660
NCBI-ProteinID: NP_057182
OMIM: 614738
HGNC: 21606
Ensembl: ENSG00000060762
UniProt: Q9Y5U8
Position
6:complement(166364919..166382940)
AA seq 109 aa
MAGALVRKAADYVRSKDFRDYLMSTHFWGPVANWGLPIAAINDMKKSPEIISGRMTFALC
CYSLTFMRFAYKVQPRNWLLFACHATNEVAQLIQGGRLIKHEMTKTASA
NT seq 330 nt   +upstreamnt  +downstreamnt
atggcgggcgcgttggtgcggaaagcggcggactatgtccgaagcaaggatttccgggac
tacctcatgagtacgcacttctggggcccagtagccaactggggtcttcccattgctgcc
atcaatgatatgaaaaagtctccagagattatcagtgggcggatgacatttgccctctgt
tgctattctttgacattcatgagatttgcctacaaggtacagcctcggaactggcttctg
tttgcatgccacgcaacaaatgaagtagcccagctcatccagggagggcggcttatcaaa
cacgagatgactaaaacggcatctgcataa

DBGET integrated database retrieval system