KEGG   Homo sapiens (human): 10008
Entry
10008             CDS       T01001                                 
Symbol
KCNE3, BRGDA6, HOKPP, HYPP, MiRP2
Name
(RefSeq) potassium voltage-gated channel subfamily E regulatory subunit 3
  KO
K04897  potassium voltage-gated channel Isk-related subfamily E member 3
Organism
hsa  Homo sapiens (human)
Pathway
hsa04974  Protein digestion and absorption
Disease
H00728  Brugada syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09154 Digestive system
   04974 Protein digestion and absorption
    10008 (KCNE3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    10008 (KCNE3)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   10008 (KCNE3)
SSDB
Motif
Pfam: ISK_Channel
Other DBs
NCBI-GeneID: 10008
NCBI-ProteinID: NP_005463
OMIM: 604433
HGNC: 6243
Ensembl: ENSG00000175538
UniProt: Q9Y6H6 Q6IAE6
Structure
Position
11:complement(74454841..74467549)
AA seq 103 aa
METTNGTETWYESLHAVLKALNATLHSNLLCRPGPGLGPDNQTEERRASLPGRDDNSYMY
ILFVMFLFAVTVGSLILGYTRSRKVDKRSDPYHVYIKNRVSMI
NT seq 312 nt   +upstreamnt  +downstreamnt
atggagactaccaatggaacggagacctggtatgagagcctgcatgccgtgctgaaggct
ctaaatgccactcttcacagcaatttgctctgccggccagggccagggctggggccagac
aaccagactgaagagaggcgggccagcctacctggccgtgatgacaactcctacatgtac
attctctttgtcatgtttctatttgctgtaactgtgggcagcctcatcctgggatacacc
cgctcccgcaaagtggacaagcgtagtgacccctatcatgtgtatatcaagaaccgtgtg
tctatgatctaa

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Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (7)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (17)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (14)   
DNA sequence (42)   
   RefSeq(nuc) (14)   
   GenBank (14)   
   EMBL (14)   
3D Structure (3)   
   PDB (3)   
Protein domain (1)   
   Pfam (1)   
All databases (77)   

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