KEGG   Homo sapiens (human): 6576
Entry
6576              CDS       T01001                                 
Symbol
SLC25A1, CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3
Name
(RefSeq) solute carrier family 25 member 1
  KO
K15100  solute carrier family 25 (mitochondrial citrate transporter), member 1
Organism
hsa  Homo sapiens (human)
Disease
H00770  Congenital myasthenic syndrome
H02304  Combined D-2- and L-2-hydroxyglutaric aciduria
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    6576 (SLC25A1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   6576 (SLC25A1)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 6576
NCBI-ProteinID: NP_005975
OMIM: 190315
HGNC: 10979
Ensembl: ENSG00000100075
UniProt: P53007
Position
22:complement(19175581..19178736)
AA seq 311 aa
MPAPRAPRALAAAAPASGKAKLTHPGKAILAGGLAGGIEICITFPTEYVKTQLQLDERSH
PPRYRGIGDCVRQTVRSHGVLGLYRGLSSLLYGSIPKAAVRFGMFEFLSNHMRDAQGRLD
STRGLLCGLGAGVAEAVVVVCPMETIKVKFIHDQTSPNPKYRGFFHGVREIVREQGLKGT
YQGLTATVLKQGSNQAIRFFVMTSLRNWYRGDNPNKPMNPLITGVFGAIAGAASVFGNTP
LDVIKTRMQGLEAHKYRNTWDCGLQILKKEGLKAFYKGTVPRLGRVCLDVAIVFVIYDEV
VKLLNKVWKTD
NT seq 936 nt   +upstreamnt  +downstreamnt
atgcccgcgccccgcgccccgcgcgctctggcggccgccgcgcccgcgtccgggaaggcc
aagctgacgcacccggggaaggcgatcctggcaggcggcctggcgggtggcatcgagatc
tgcatcaccttccccaccgagtacgtgaagacgcagctgcagctggacgagcgctcgcac
ccgccgcggtaccggggcatcggggactgcgtgcggcagacggttcgcagccatggcgtc
ctgggcctgtaccgcggccttagctccctgctctacggttccatccccaaggcggccgtc
aggtttggaatgttcgagttcctcagcaaccacatgcgggatgcccagggacggctggac
agcacgcgtgggctgctgtgcggcctgggcgctggcgtggccgaggccgtggtggtcgtg
tgccccatggagaccatcaaggtgaagttcatccacgaccagacctccccaaaccccaag
tacagaggattcttccacggggttagggagattgtgcgggaacaagggctgaaggggacg
taccagggcctcacagccactgtcctgaagcagggctcgaaccaggccatccgcttcttc
gtcatgacctccctgcgcaactggtaccgaggggacaaccccaacaagcccatgaaccct
ctgatcactggggtcttcggagctattgcaggcgcagccagtgtctttggaaacactcct
ctggatgtgattaagacccggatgcagggcctggaggcgcacaaataccggaacacgtgg
gactgcggcttgcagatcctgaagaaggaggggctcaaggcattctacaagggcactgtc
ccccgcctgggccgggtctgcctggatgtggccatagtgtttgtcatctatgatgaagtg
gtgaagctgctcaacaaagtgtggaagacggactaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (18)   
   KEGG ORTHOLOGY (1)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (8)   
   OC (1)   
Protein sequence (5)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (44)   
   RefSeq(nuc) (4)   
   GenBank (20)   
   EMBL (20)   
Protein domain (1)   
   Pfam (1)   
All databases (76)   

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