KEGG   Homo sapiens (human): 79751
Entry
79751             CDS       T01001                                 
Symbol
SLC25A22, DEE3, EIEE3, GC-1, GC1, NET44
Name
(RefSeq) solute carrier family 25 member 22
  KO
K15107  solute carrier family 25 (mitochondrial glutamate transporter), member 18/22
Organism
hsa  Homo sapiens (human)
Disease
H00606  Early infantile epileptic encephalopathy
H01819  Early myoclonic encephalopathy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    79751 (SLC25A22)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   79751 (SLC25A22)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 79751
NCBI-ProteinID: NP_001177989
OMIM: 609302
HGNC: 19954
Ensembl: ENSG00000177542
UniProt: Q9H936
Position
11:complement(790475..798281)
AA seq 323 aa
MADKQISLPAKLINGGIAGLIGVTCVFPIDLAKTRLQNQQNGQRVYTSMSDCLIKTVRSE
GYFGMYRGAAVNLTLVTPEKAIKLAANDFFRHQLSKDGQKLTLLKEMLAGCGAGTCQVIV
TTPMEMLKIQLQDAGRIAAQRKILAAQGQLSAQGGAQPSVEAPAAPRPTATQLTRDLLRS
RGIAGLYKGLGATLLRDVPFSVVYFPLFANLNQLGRPASEEKSPFYVSFLAGCVAGSAAA
VAVNPCDVVKTRLQSLQRGVNEDTYSGILDCARKILRHEGPSAFLKGAYCRALVIAPLFG
IAQVVYFLGIAESLLGLLQDPQA
NT seq 972 nt   +upstreamnt  +downstreamnt
atggctgataagcagatcagcctgccagccaagctcatcaatggcggcatcgccgggctg
atcggtgtcacctgcgtgtttcccatcgacctggccaagaccaggctgcagaaccagcag
aacggccagcgcgtgtacacgagcatgtccgactgcctcatcaagaccgtccgctccgag
ggctacttcggcatgtaccggggagctgctgtgaacttgaccctcgtcacccccgagaag
gccatcaagctggcagccaacgacttcttccgacatcagctctctaaggacgggcagaag
ctgaccctgcttaaagagatgctggcgggctgtggggctggcacctgccaggtgatcgtg
accacgcccatggagatgctgaagatccagctgcaggatgcagggcgcattgccgcccag
aggaagatcctggctgcccagggccagctctcggcccaggggggtgcccagccctcagtg
gaggctccagctgcccctcggcccacggccacccagctgacccgcgacctgctgcggagc
cgtggcattgccggtctctacaagggactcggggccacgctgctcagggatgtccccttc
tctgtggtgtacttcccgctctttgccaacctgaaccagctgggccgcccggcgtccgag
gagaagtcgcctttctacgtgtccttcctggccggctgtgtggctgggagtgccgccgct
gtggccgtcaacccctgtgatgtggtgaagacgcggctccagtcacttcagcgaggcgtc
aacgaggacacctactctgggatcctggactgtgccaggaagatcctgcggcacgagggc
ccctcggccttcctgaagggcgcctactgccgcgcgctggtcatcgcgccccttttcggc
atcgcacaggtggtctacttcctgggcatcgcggagtccctgctggggctgctgcaggac
ccccaggcctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (4)   
   KEGG DISEASE (2)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (12)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (34)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (32)   
DNA sequence (50)   
   RefSeq(nuc) (32)   
   GenBank (9)   
   EMBL (9)   
Protein domain (1)   
   Pfam (1)   
All databases (104)   

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