KEGG   Homo sapiens (human): 3788
Entry
3788              CDS       T01001                                 
Symbol
KCNS2, KV9.2
Name
(RefSeq) potassium voltage-gated channel modifier subfamily S member 2
  KO
K04932  potassium voltage-gated channel delayed-rectifier subfamily S member 2
Organism
hsa  Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3788 (KCNS2)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   3788 (KCNS2)
SSDB
Motif
Pfam: Ion_trans BTB_2 Ion_trans_2
Other DBs
NCBI-GeneID: 3788
NCBI-ProteinID: NP_065748
OMIM: 602906
HGNC: 6301
Ensembl: ENSG00000156486
UniProt: Q9ULS6
Position
8:98426958..98432853
AA seq 477 aa
MTGQSLWDVSEANVEDGEIRINVGGFKRRLRSHTLLRFPETRLGRLLLCHSREAILELCD
DYDDVQREFYFDRNPELFPYVLHFYHTGKLHVMAELCVFSFSQEIEYWGINEFFIDSCCS
YSYHGRKVEPEQEKWDEQSDQESTTSSFDEILAFYNDASKFDGQPLGNFRRQLWLALDNP
GYSVLSRVFSILSILVVMGSIITMCLNSLPDFQIPDSQGNPGEDPRFEIVEHFGIAWFTF
ELVARFAVAPDFLKFFKNALNLIDLMSIVPFYITLVVNLVVESTPTLANLGRVAQVLRLM
RIFRILKLARHSTGLRSLGATLKYSYKEVGLLLLYLSVGISIFSVVAYTIEKEENEGLAT
IPACWWWATVSMTTVGYGDVVPGTTAGKLTASACILAGILVVVLPITLIFNKFSHFYRRQ
KQLESAMRSCDFGDGMKEVPSVNLRDYYAHKVKSLMASLTNMSRSSPSELSLNDSLR
NT seq 1434 nt   +upstreamnt  +downstreamnt
atgaccggccagagcctgtgggacgtgtcggaggctaacgtcgaggacggggagatccgc
atcaatgtgggcggcttcaagaggaggctgcgctcgcacacgctgctgcgcttccccgag
acgcgcctgggccgcttgctgctctgccactcgcgcgaggccattctggagctctgcgat
gactacgacgacgtccagcgggagttctacttcgaccgcaaccctgagctcttcccctac
gtgctgcatttctatcacaccggcaagcttcacgtcatggctgagctatgtgtcttctcc
ttcagccaggagatcgagtactggggcatcaacgagttcttcattgactcctgctgcagc
tacagctaccatggccgcaaagtagagcccgagcaggagaagtgggacgagcagagtgac
caggagagcaccacgtcttccttcgatgagatccttgccttctacaacgacgcctccaag
ttcgatgggcagcccctcggcaacttccgcaggcagctgtggctggcgctggacaacccc
ggctactcagtgctgagcagggtcttcagcatcctgtccatcctggtggtgatggggtcc
atcatcaccatgtgcctcaatagcctgcccgatttccaaatccctgacagccagggcaac
cctggcgaggaccctaggttcgaaatcgtggagcactttggcattgcctggttcacattt
gagctggtggccaggtttgctgtggcccctgacttcctcaagttcttcaagaatgcccta
aaccttattgacctcatgtccatcgtccccttttacatcactctggtggtgaacctggtg
gtggagagcacacctactttagccaacttgggcagggtggcccaggtcctgaggctgatg
cggatcttccgcatcttaaagctggccaggcactccactggcctccgctccctgggggcc
actttgaaatacagctacaaagaagtagggctgctcttgctctacctctccgtggggatt
tccatcttctccgtggtggcctacaccattgaaaaggaggagaacgagggcctggccacc
atccctgcctgctggtggtgggctaccgtcagtatgaccacagtggggtacggggatgtg
gtcccagggaccacggcaggaaagctgactgcctctgcctgcatcttggcaggcatcctc
gtggtggtcctgcccatcaccttgatcttcaataagttctcccacttttaccggcgccaa
aagcaacttgagagtgccatgcgcagctgtgactttggagatggaatgaaggaggtccct
tcggtcaatttaagggactattatgcccataaagttaaatcccttatggcaagcctgacg
aacatgagcaggagctcaccaagtgaactcagtttaaatgattccctacgttag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (12)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (11)   
   RefSeq(nuc) (1)   
   GenBank (5)   
   EMBL (5)   
Protein domain (3)   
   Pfam (3)   
All databases (33)   

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