KEGG   Homo sapiens (human): 788
Entry
788               CDS       T01001                                 
Symbol
SLC25A20, CAC, CACT
Name
(RefSeq) solute carrier family 25 member 20
  KO
K15109  solute carrier family 25 (mitochondrial carnitine/acylcarnitine transporter), member 20/29
Organism
hsa  Homo sapiens (human)
Pathway
hsa04714  Thermogenesis
Network
nt06020  beta-Oxidation in mitochondria
  Element
N00814  Transport of L-palmitoylcarnitine
Disease
H00525  Disorders of mitochondrial fatty-acid oxidation
H01400  Secondary hyperammonemia
H01983  Carnitine-acylcarnitine translocase deficiency
H02596  Disorders of carnitine transport and the carnitine cycle
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    788 (SLC25A20)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    788 (SLC25A20)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   788 (SLC25A20)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 788
NCBI-ProteinID: NP_000378
OMIM: 613698
HGNC: 1421
Ensembl: ENSG00000178537
UniProt: O43772
Position
3:complement(48856926..48898882)
AA seq 301 aa
MADQPKPISPLKNLLAGGFGGVCLVFVGHPLDTVKVRLQTQPPSLPGQPPMYSGTFDCFR
KTLFREGITGLYRGMAAPIIGVTPMFAVCFFGFGLGKKLQQKHPEDVLSYPQLFAAGMLS
GVFTTGIMTPGERIKCLLQIQASSGESKYTGTLDCAKKLYQEFGIRGIYKGTVLTLMRDV
PASGMYFMTYEWLKNIFTPEGKRVSELSAPRILVAGGIAGIFNWAVAIPPDVLKSRFQTA
PPGKYPNGFRDVLRELIRDEGVTSLYKGFNAVMIRAFPANAACFLGFEVAMKFLNWATPN
L
NT seq 906 nt   +upstreamnt  +downstreamnt
atggccgaccagccaaaacccatcagcccgctcaagaacctgctggccggcggctttggc
ggcgtgtgcctggtgttcgtcggtcaccctctggacacggtcaaggtccgactgcagaca
cagccaccgagtttgcctggacaacctcccatgtactctgggacctttgactgtttccgg
aagactctttttagagagggcatcacggggctatatcggggaatggctgcccctatcatc
ggggtcactcccatgtttgccgtgtgcttctttgggtttggtttggggaagaaactacaa
cagaaacacccagaagatgtgctcagctatccccagctttttgcagctgggatgttatct
ggcgtattcaccacaggaatcatgactcctggagaacggatcaagtgcttattacagatt
caggcttcttcaggagaaagcaagtacactggtaccttggactgtgcaaagaagctgtac
caggagtttgggatccgaggcatctacaaagggactgtgcttacccttatgcgagatgtc
ccagctagtggaatgtatttcatgacatatgaatggctgaaaaatatcttcactccggag
ggaaagagggtcagtgagctcagtgcccctcggatcttggtggctgggggcattgcaggg
atcttcaactgggctgtggcaatccccccagatgtgctcaagtctcgattccagactgca
cctcctgggaaatatcctaatggtttcagagatgtgctgagggagctgatccgggatgaa
ggagtcacatccttgtacaaagggttcaatgcagtgatgatccgagccttcccagccaat
gcggcctgtttccttggctttgaagttgccatgaagttccttaattgggccacccccaac
ttgtga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Network (2)   
   KEGG NETWORK (2)   
Disease (6)   
   KEGG DISEASE (4)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (13)   
   KEGG ORTHOLOGY (1)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (15)   
   RefSeq(nuc) (1)   
   GenBank (7)   
   EMBL (7)   
Protein domain (1)   
   Pfam (1)   
All databases (44)   

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