KEGG   Homo sapiens (human): 3750
Entry
3750              CDS       T01001                                 
Symbol
KCND1, KV4.1
Name
(RefSeq) potassium voltage-gated channel subfamily D member 1
  KO
K04891  potassium voltage-gated channel Shal-related subfamily D member 1
Organism
hsa  Homo sapiens (human)
Network
nt06462  Spinocerebellar ataxia
  Element
N00974  Transport of potassium
Drug target
Amifampridine: D10228 D10689<US>
Butamben (DG02875): D00730
Clofilium phosphate: D03547
Fampridine: D04127<US>
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3750 (KCND1)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   3750 (KCND1)
SSDB
Motif
Pfam: Ion_trans DUF3399 BTB_2 Ion_trans_2 Shal-type BTB_3 PKD_channel
Other DBs
NCBI-GeneID: 3750
NCBI-ProteinID: NP_004970
OMIM: 300281
HGNC: 6237
Ensembl: ENSG00000102057
UniProt: Q9NSA2
LinkDB
Position
X:complement(48961380..48971844)
AA seq 647 aa
MAAGLATWLPFARAAAVGWLPLAQQPLPPAPGVKASRGDEVLVVNVSGRRFETWKNTLDR
YPDTLLGSSEKEFFYDADSGEYFFDRDPDMFRHVLNFYRTGRLHCPRQECIQAFDEELAF
YGLVPELVGDCCLEEYRDRKKENAERLAEDEEAEQAGDGPALPAGSSLRQRLWRAFENPH
TSTAALVFYYVTGFFIAVSVIANVVETIPCRGSARRSSREQPCGERFPQAFFCMDTACVL
IFTGEYLLRLFAAPSRCRFLRSVMSLIDVVAILPYYIGLLVPKNDDVSGAFVTLRVFRVF
RIFKFSRHSQGLRILGYTLKSCASELGFLLFSLTMAIIIFATVMFYAEKGTNKTNFTSIP
AAFWYTIVTMTTLGYGDMVPSTIAGKIFGSICSLSGVLVIALPVPVIVSNFSRIYHQNQR
ADKRRAQQKVRLARIRLAKSGTTNAFLQYKQNGGLEDSGSGEEQALCVRNRSAFEQQHHH
LLHCLEKTTCHEFTDELTFSEALGAVSPGGRTSRSTSVSSQPVGPGSLLSSCCPRRAKRR
AIRLANSTASVSRGSMQELDMLAGLRRSHAPQSRSSLNAKPHDSLDLNCDSRDFVAAIIS
IPTPPANTPDESQPSSPGGGGRAGSTLRNSSLGTPCLFPETVKISSL
NT seq 1944 nt   +upstreamnt  +downstreamnt
atggcggcaggcctggccacgtggctgccttttgctcgggcagcagcagtgggctggctg
cccctggcccagcaacccctgcccccggcaccgggggtgaaggcatctcgaggagatgag
gttctggtggtgaacgtgagcggacggcgctttgagacttggaagaatacgctggaccgc
tacccagacaccttgctgggcagctcggagaaggaattcttctacgatgctgactcaggc
gagtacttcttcgatcgcgaccctgacatgttccgccatgtgctgaacttctaccgaacg
gggcggctgcattgcccacggcaggagtgcatccaggccttcgacgaagagctggctttc
tacggcctggttcccgagctagtcggtgactgctgccttgaagagtatcgggaccgaaag
aaggagaatgccgagcgcctggcagaggatgaggaggcagagcaggccggggacggccca
gccctgccagcaggcagctccctgcggcagcggctctggcgggccttcgagaatccacac
acgagcaccgcagccctcgttttctactatgtgaccggcttcttcatcgccgtgtcggtc
atcgccaatgtggtggagaccatcccatgccgcggctctgcacgcaggtcctcaagggag
cagccctgtggcgaacgcttcccacaggcctttttctgcatggacacagcctgtgtactc
atattcacaggtgaatacctcctgcggctgtttgccgcccccagccgttgccgcttcctg
cggagtgtcatgagcctcatcgacgtggtggccatcctgccctactacattgggcttttg
gtgcccaagaacgacgatgtctctggcgcctttgtcaccctgcgtgtgttccgggtgttt
cgcatcttcaagttctccaggcactcacagggcttgaggattctgggctacacactcaag
agctgtgcctctgagctgggctttctcctcttttccctaaccatggccatcatcatcttt
gccactgtcatgttttatgctgagaagggcacaaacaagaccaactttacaagcatccct
gcggccttctggtataccattgtcaccatgaccacgcttggctacggagacatggtgccc
agcaccattgctggcaagattttcgggtccatctgctcactcagtggcgtcttggtcatt
gccctgcctgtgccagtcattgtgtccaactttagccgcatctaccaccagaaccagcgg
gctgacaagcgccgagcacagcagaaggtgcgcttggcaaggatccgattggcaaagagt
ggtaccaccaatgccttcctgcagtacaagcagaatgggggccttgaggacagcggcagt
ggcgaggaacaggctctttgtgtcaggaaccgttctgcctttgaacagcaacatcaccac
ttgctgcactgtctagagaagacaacgtgccatgagttcacagatgagctcaccttcagt
gaagccctgggagccgtctcgccgggtggccgcaccagccgtagcacctctgtgtcttcc
cagccagtgggacccggaagcctgctgtcttcttgctgccctcgcagggccaagcgccgc
gccatccgccttgccaactccactgcctcagtcagccgtggcagcatgcaggagctggac
atgctggcagggctgcgcaggagccatgcccctcagagccgttccagcctcaatgccaag
ccccatgacagccttgacctgaactgcgacagccgggacttcgtggctgccattatcagc
atccctacccctcctgccaacaccccagatgagagccaaccttcctcccctggcggcggt
ggcagggccggcagcaccctcaggaactccagcctgggtaccccttgcctcttccccgag
actgtcaagatctcatccctgtga

KEGG   Homo sapiens (human): 3751
Entry
3751              CDS       T01001                                 
Symbol
KCND2, KV4.2, RK5
Name
(RefSeq) potassium voltage-gated channel subfamily D member 2
  KO
K04892  potassium voltage-gated channel Shal-related subfamily D member 2
Organism
hsa  Homo sapiens (human)
Pathway
hsa04726  Serotonergic synapse
Network
nt06462  Spinocerebellar ataxia
  Element
N00974  Transport of potassium
Drug target
Amifampridine: D10228 D10689<US>
Butamben (DG02875): D00730
Clofilium phosphate: D03547
Fampridine: D04127<US>
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09156 Nervous system
   04726 Serotonergic synapse
    3751 (KCND2)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3751 (KCND2)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   3751 (KCND2)
SSDB
Motif
Pfam: Ion_trans DUF3399 BTB_2 Ion_trans_2 Shal-type BTB_3 PKD_channel
Other DBs
NCBI-GeneID: 3751
NCBI-ProteinID: NP_036413
OMIM: 605410
HGNC: 6238
Ensembl: ENSG00000184408
UniProt: Q9NZV8 A4D0V9
Structure
LinkDB
Position
7:120272908..120750337
AA seq 630 aa
MAAGVAAWLPFARAAAIGWMPVASGPMPAPPRQERKRTQDALIVLNVSGTRFQTWQDTLE
RYPDTLLGSSERDFFYHPETQQYFFDRDPDIFRHILNFYRTGKLHYPRHECISAYDEELA
FFGLIPEIIGDCCYEEYKDRRRENAERLQDDADTDTAGESALPTMTARQRVWRAFENPHT
STMALVFYYVTGFFIAVSVIANVVETVPCGSSPGHIKELPCGERYAVAFFCLDTACVMIF
TVEYLLRLAAAPSRYRFVRSVMSIIDVVAILPYYIGLVMTDNEDVSGAFVTLRVFRVFRI
FKFSRHSQGLRILGYTLKSCASELGFLLFSLTMAIIIFATVMFYAEKGSSASKFTSIPAA
FWYTIVTMTTLGYGDMVPKTIAGKIFGSICSLSGVLVIALPVPVIVSNFSRIYHQNQRAD
KRRAQKKARLARIRAAKSGSANAYMQSKRNGLLSNQLQSSEDEQAFVSKSGSSFETQHHH
LLHCLEKTTNHEFVDEQVFEESCMEVATVNRPSSHSPSLSSQQGVTSTCCSRRHKKTFRI
PNANVSGSHQGSIQELSTIQIRCVERTPLSNSRSSLNAKMEECVKLNCEQPYVTTAIISI
PTPPVTTPEGDDRPESPEYSGGNIVRVSAL
NT seq 1893 nt   +upstreamnt  +downstreamnt
atggcggcgggggtggcagcgtggctgccttttgcaagggcagcggctatcgggtggatg
cctgtggcctcggggcctatgccggctcccccgaggcaggagaggaaaaggacccaagat
gctctcattgtgctgaatgtgagtggcacccgcttccagacgtggcaggacaccctggaa
cgttacccagacactctactgggcagttctgagagggactttttctaccacccagaaact
cagcagtatttctttgaccgtgacccagacatcttccgccacatcctgaatttctaccgc
actgggaagctccactatcctcgccacgagtgcatctctgcttacgatgaagaactggcc
ttctttggcctcatcccggaaatcatcggcgactgctgttatgaggagtacaaggatcgc
aggcgagagaacgccgagcgcctgcaggacgacgcggataccgacaccgctggggagagc
gccttgcccaccatgactgcaaggcagagggtctggagggccttcgagaacccccacacc
agcacgatggccctggtgttctactatgtcacggggtttttcattgccgtctctgtcatc
gcgaatgtggtggaaacagtgccgtgcggatcaagcccaggtcacattaaagaactgccc
tgtggagagcggtatgctgtggccttcttctgcttggacacggcctgcgtcatgatcttc
acagttgagtatttgcttcgcctggctgcagcgcctagtcgttaccgttttgtgcgtagt
gtcatgagtatcatcgacgtggtggccatcctgccttattacattgggctggtgatgaca
gacaatgaggacgtcagcggagcctttgtcacactccgagtcttccgggtcttcaggatc
tttaagttttcccgccactctcaaggcctgcgcatcctggggtacacactgaagagttgt
gcctcagaattgggcttcttgcttttctcgctcaccatggctatcatcatcttcgctaca
gttatgttctacgcagagaaggggtcttcggctagcaagttcaccagcatccctgcagcc
ttctggtataccatcgtcaccatgacaacactagggtatggtgacatggtgccaaaaacc
atagcagggaagatttttggttctatctgttcgctgagtggggtcttggtcattgctcta
cctgttccggtgattgtatccaacttcagtcgcatctaccaccagaatcaacgagcagac
aaacgaagggcacaaaagaaagctagactggccaggatccgggcagccaaaagcggaagc
gcaaatgcttacatgcagagcaaacggaatggtttactcagtaatcagctgcagtcctca
gaggatgagcaggcttttgttagcaaatccggctccagctttgaaacccagcaccaccac
ctgcttcactgcctggaaaaaaccacgaatcacgagtttgtggacgaacaagtctttgaa
gaaagctgcatggaagttgcaactgttaatcgtccttcaagtcacagtccttcactgtct
tcacaacaaggagtcaccagcacctgctgttcacgacgacacaaaaaaacttttcgcatc
ccaaatgccaatgtatcaggaagccatcaaggtagtatacaagaactcagcacgattcag
atcagatgtgtggagagaacacctctgtctaacagccgatccagtttaaatgccaaaatg
gaagagtgtgttaaactaaactgtgaacaaccttatgtgactacagcaataataagcatc
ccaacacctccagtaaccacaccagaaggagacgataggccagaatcccctgagtactca
ggaggaaatattgtcagagtttctgctttgtaa

KEGG   Homo sapiens (human): 3752
Entry
3752              CDS       T01001                                 
Symbol
KCND3, BRGDA9, KCND3L, KCND3S, KSHIVB, KV4.3, SCA19, SCA22
Name
(RefSeq) potassium voltage-gated channel subfamily D member 3
  KO
K04893  potassium voltage-gated channel Shal-related subfamily D member 3
Organism
hsa  Homo sapiens (human)
Pathway
hsa05017  Spinocerebellar ataxia
Network
nt06462  Spinocerebellar ataxia
  Element
N00974  Transport of potassium
N00975  Mutation-inactivated KCND3 to transport of potassium
Disease
H00063  Spinocerebellar ataxia (SCA)
H00728  Brugada syndrome
Drug target
Amifampridine: D10228 D10689<US>
Amiodarone (DG00204): D00636<JP/US> D02910
Bepridil (DG00333): D00631<JP> D07520
Butamben (DG02875): D00730
Clofilium phosphate: D03547
Dronedarone (DG00207): D02537 D03914<US>
Fampridine: D04127<US>
Nifekalant hydrochloride: D01856<JP>
Vernakalant: D06665
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09164 Neurodegenerative disease
   05017 Spinocerebellar ataxia
    3752 (KCND3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3752 (KCND3)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   3752 (KCND3)
SSDB
Motif
Pfam: Ion_trans DUF3399 BTB_2 Shal-type Ion_trans_2 BTB_3 PKD_channel
Other DBs
NCBI-GeneID: 3752
NCBI-ProteinID: NP_004971
OMIM: 605411
HGNC: 6239
Ensembl: ENSG00000171385
UniProt: Q9UK17
Structure
LinkDB
Position
1:complement(111770662..111989668)
AA seq 655 aa
MAAGVAAWLPFARAAAIGWMPVANCPMPLAPADKNKRQDELIVLNVSGRRFQTWRTTLER
YPDTLLGSTEKEFFFNEDTKEYFFDRDPEVFRCVLNFYRTGKLHYPRYECISAYDDELAF
YGILPEIIGDCCYEEYKDRKRENAERLMDDNDSENNQESMPSLSFRQTMWRAFENPHTST
LALVFYYVTGFFIAVSVITNVVETVPCGTVPGSKELPCGERYSVAFFCLDTACVMIFTVE
YLLRLFAAPSRYRFIRSVMSIIDVVAIMPYYIGLVMTNNEDVSGAFVTLRVFRVFRIFKF
SRHSQGLRILGYTLKSCASELGFLLFSLTMAIIIFATVMFYAEKGSSASKFTSIPASFWY
TIVTMTTLGYGDMVPKTIAGKIFGSICSLSGVLVIALPVPVIVSNFSRIYHQNQRADKRR
AQKKARLARIRVAKTGSSNAYLHSKRNGLLNEALELTGTPEEEHMGKTTSLIESQHHHLL
HCLEKTTGLSYLVDDPLLSVRTSTIKNHEFIDEQMFEQNCMESSMQNYPSTRSPSLSSHP
GLTTTCCSRRSKKTTHLPNSNLPATRLRSMQELSTIHIQGSEQPSLTTSRSSLNLKADDG
LRPNCKTSQITTAIISIPTPPALTPEGESRPPPASPGPNTNIPSIASNVVKVSAL
NT seq 1968 nt   +upstreamnt  +downstreamnt
atggcggccggagttgcggcctggctgccttttgcccgggctgcggccatcgggtggatg
ccggtggccaactgccccatgcccctggccccggccgacaagaacaagcggcaggatgag
ctgattgtcctcaacgtgagtgggcggaggttccagacctggaggaccacgctggagcgc
tacccggacaccctgctgggcagcacggagaaggagttcttcttcaacgaggacaccaag
gagtacttcttcgaccgggaccccgaggtgttccgctgcgtgctcaacttctaccgcacg
gggaagctgcactacccgcgctacgagtgcatctctgcctacgacgacgagctggccttc
tacggcatcctcccggagatcatcggggactgctgctacgaggagtacaaggaccgcaag
agggagaacgccgagcggctcatggacgacaacgactcggagaacaaccaggagtccatg
ccctcgctcagcttccgccagaccatgtggcgggccttcgagaacccccacaccagcacg
ctggccctggtcttctactacgtgactggcttcttcatcgctgtctcggtcatcaccaac
gtggtggagacggtgccgtgcggcacggtcccgggcagcaaggagctgccgtgcggggag
cgctactcggtggccttcttctgcctggacacggcgtgcgtcatgatcttcaccgtggag
tacctcctgcggctcttcgcggctcccagccgctaccgcttcatccgcagcgtcatgagc
atcatcgacgtggtggccatcatgccctactacatcggtctggtcatgaccaacaacgag
gacgtgtccggcgccttcgtcacgctccgggtcttccgcgtcttcaggatcttcaagttt
tcccgccactcccagggcctgcggatcctgggctacacactgaagagctgtgcctccgaa
ctgggctttcttctcttctccctcaccatggccatcatcatctttgccactgtgatgttt
tatgccgagaagggctcctcggccagcaagttcacaagcatccctgcctcgttttggtac
accattgtcaccatgaccacactgggatacggagacatggtgcctaagacgattgcaggg
aagatcttcggctccatctgctccttgagtggcgtcctggtcattgccctgccagtccct
gtgattgtttccaactttagccggatttaccaccagaatcagagagctgataaacgcagg
gcacaaaagaaggcccgccttgccaggatccgtgtggccaaaacaggcagttcgaatgca
tacctgcacagcaagcgcaacgggctcctcaacgaggcgctggagctgacgggcacccca
gaagaggagcacatgggcaagaccacctcactcatcgagagccagcatcatcacctgctg
cactgcctggaaaaaaccactgggttgtcctatcttgtggatgatcccctgttatctgta
cgaacctccaccatcaagaaccacgagtttattgatgagcagatgtttgagcagaactgc
atggagagttcaatgcagaactacccatccacaagaagtccctcactgtccagccaccca
ggcctcactaccacctgctgctcccgtcgtagtaagaagaccacacacctgcccaattct
aacctgccagctactcgcctgcgcagcatgcaagagctcagcacgatccacatccagggc
agtgagcagccctccctcacaaccagtcgctccagccttaatttgaaagcagacgacgga
ctgagaccaaactgcaaaacatcccagatcaccacagccatcatcagcatccccactccc
ccagcgctaaccccagagggggaaagtcggccaccccctgccagcccaggccccaacacg
aacattccttccatagccagcaatgttgtcaaggtctccgccttgtaa

DBGET integrated database retrieval system