KEGG   Homo sapiens (human): 91137
Entry
91137             CDS       T01001                                 
Symbol
SLC25A46, HMSN6B, PCH1E
Name
(RefSeq) solute carrier family 25 member 46
  KO
K03454  solute carrier family 25, member 46
Organism
hsa  Homo sapiens (human)
Disease
H00264  Charcot-Marie-Tooth disease
H00897  Pontocerebellar hypoplasia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    91137 (SLC25A46)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   91137 (SLC25A46)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 91137
NCBI-ProteinID: NP_620128
OMIM: 610826
HGNC: 25198
Ensembl: ENSG00000164209
UniProt: Q96AG3
Position
5:110738145..110765157
AA seq 418 aa
MHPRRPDGFDGLGYRGGARDEQGFGGAFPARSFSTGSDLGHWVTTPPDIPGSRNLHWGEK
SPPYGVPTTSTPYEGPTEEPFSSGGGGSVQGQSSEQLNRFAGFGIGLASLFTENVLAHPC
IVLRRQCQVNYHAQHYHLTPFTVINIMYSFNKTQGPRALWKGMGSTFIVQGVTLGAEGII
SEFTPLPREVLHKWSPKQIGEHLLLKSLTYVVAMPFYSASLIETVQSEIIRDNTGILECV
KEGIGRVIGMGVPHSKRLLPLLSLIFPTVLHGVLHYIISSVIQKFVLLILKRKTYNSHLA
ESTSPVQSMLDAYFPELIANFAASLCSDVILYPLETVLHRLHIQGTRTIIDNTDLGYEVL
PINTQYEGMRDCINTIRQEEGVFGFYKGFGAVIIQYTLHAAVLQITKIIYSTLLQNNI
NT seq 1257 nt   +upstreamnt  +downstreamnt
atgcatccgcggcgcccggacggatttgatggcttgggctaccggggtggtgcccgggac
gagcagggctttggcggcgccttccctgcaaggtccttcagcaccgggtcggacctgggc
cactgggtgacgactcccccagatatccccggcagccgcaacctgcactggggcgagaag
agcccgccctacggcgtgcccaccacctccaccccgtacgaaggccccacggaggaaccc
ttttccagtggcggcggcggcagtgtgcaggggcagagcagtgaacagctgaatagattt
gctggatttggtattggacttgcaagtctctttacagaaaatgtattggcacatccttgc
attgttctacgccgccaatgtcaggttaattaccatgctcagcattaccatctcactcca
tttacagtcatcaatattatgtacagtttcaacaaaactcagggacctagagccctgtgg
aaaggaatgggaagtacatttattgtccagggagtcacacttggagcagaaggcataatt
agtgaatttacacctttgccaagggaggttttacataaatggagtcctaaacaaatagga
gaacaccttctactgaaatccctaacttacgtggtggcaatgcctttttattcagcaagt
ctgattgaaacagtgcagagtgagataattcgagataatactggcattttggagtgtgtt
aaagaaggaattggaagagtgataggcatgggagtgcctcatagcaaacgacttcttccg
cttctttccttgatcttccctacggtgcttcatggagttcttcattacatcatcagctca
gttattcagaagtttgtcctactaattctaaagagaaagacttacaatagccacctagct
gagagcactagccctgtgcagagtatgttggatgcttattttccagaacttattgctaac
tttgctgccagtctttgttctgacgttatactttacccattggaaacagttttgcaccgc
cttcacattcaaggaacacgcacaataattgacaatacagaccttggctatgaagtgctt
ccaattaatacacaatatgagggaatgagagactgtatcaataccataaggcaggaggaa
ggagtgtttggtttttataaagggtttggtgctgttataatacagtacacactgcatgca
gctgttttacagattaccaaaattatttactctacacttcttcaaaataacatttga

  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 (9)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (5)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (22)   
   RefSeq(nuc) (4)   
   GenBank (9)   
   EMBL (9)   
Protein domain (1)   
   Pfam (1)   
All databases (54)   

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