Homo sapiens (human): 3750
Help
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ion_trans
DUF3399
BTB_2
Ion_trans_2
Shal-type
BTB_3
PKD_channel
Motif
Other DBs
NCBI-GeneID:
3750
NCBI-ProteinID:
NP_004970
OMIM:
300281
HGNC:
6237
Ensembl:
ENSG00000102057
UniProt:
Q9NSA2
LinkDB
All DBs
Position
X:complement(48961380..48971844)
Genome browser
AA seq
647 aa
AA seq
DB search
MAAGLATWLPFARAAAVGWLPLAQQPLPPAPGVKASRGDEVLVVNVSGRRFETWKNTLDR
YPDTLLGSSEKEFFYDADSGEYFFDRDPDMFRHVLNFYRTGRLHCPRQECIQAFDEELAF
YGLVPELVGDCCLEEYRDRKKENAERLAEDEEAEQAGDGPALPAGSSLRQRLWRAFENPH
TSTAALVFYYVTGFFIAVSVIANVVETIPCRGSARRSSREQPCGERFPQAFFCMDTACVL
IFTGEYLLRLFAAPSRCRFLRSVMSLIDVVAILPYYIGLLVPKNDDVSGAFVTLRVFRVF
RIFKFSRHSQGLRILGYTLKSCASELGFLLFSLTMAIIIFATVMFYAEKGTNKTNFTSIP
AAFWYTIVTMTTLGYGDMVPSTIAGKIFGSICSLSGVLVIALPVPVIVSNFSRIYHQNQR
ADKRRAQQKVRLARIRLAKSGTTNAFLQYKQNGGLEDSGSGEEQALCVRNRSAFEQQHHH
LLHCLEKTTCHEFTDELTFSEALGAVSPGGRTSRSTSVSSQPVGPGSLLSSCCPRRAKRR
AIRLANSTASVSRGSMQELDMLAGLRRSHAPQSRSSLNAKPHDSLDLNCDSRDFVAAIIS
IPTPPANTPDESQPSSPGGGGRAGSTLRNSSLGTPCLFPETVKISSL
NT seq
1944 nt
NT seq
+upstream
nt +downstream
nt
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
Homo sapiens (human): 3751
Help
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ion_trans
DUF3399
BTB_2
Ion_trans_2
Shal-type
BTB_3
PKD_channel
Motif
Other DBs
NCBI-GeneID:
3751
NCBI-ProteinID:
NP_036413
OMIM:
605410
HGNC:
6238
Ensembl:
ENSG00000184408
UniProt:
Q9NZV8
A4D0V9
Structure
PDB
LinkDB
All DBs
Position
7:120272908..120750337
Genome browser
AA seq
630 aa
AA seq
DB search
MAAGVAAWLPFARAAAIGWMPVASGPMPAPPRQERKRTQDALIVLNVSGTRFQTWQDTLE
RYPDTLLGSSERDFFYHPETQQYFFDRDPDIFRHILNFYRTGKLHYPRHECISAYDEELA
FFGLIPEIIGDCCYEEYKDRRRENAERLQDDADTDTAGESALPTMTARQRVWRAFENPHT
STMALVFYYVTGFFIAVSVIANVVETVPCGSSPGHIKELPCGERYAVAFFCLDTACVMIF
TVEYLLRLAAAPSRYRFVRSVMSIIDVVAILPYYIGLVMTDNEDVSGAFVTLRVFRVFRI
FKFSRHSQGLRILGYTLKSCASELGFLLFSLTMAIIIFATVMFYAEKGSSASKFTSIPAA
FWYTIVTMTTLGYGDMVPKTIAGKIFGSICSLSGVLVIALPVPVIVSNFSRIYHQNQRAD
KRRAQKKARLARIRAAKSGSANAYMQSKRNGLLSNQLQSSEDEQAFVSKSGSSFETQHHH
LLHCLEKTTNHEFVDEQVFEESCMEVATVNRPSSHSPSLSSQQGVTSTCCSRRHKKTFRI
PNANVSGSHQGSIQELSTIQIRCVERTPLSNSRSSLNAKMEECVKLNCEQPYVTTAIISI
PTPPVTTPEGDDRPESPEYSGGNIVRVSAL
NT seq
1893 nt
NT seq
+upstream
nt +downstream
nt
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
Homo sapiens (human): 3752
Help
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ion_trans
DUF3399
BTB_2
Shal-type
Ion_trans_2
BTB_3
PKD_channel
Motif
Other DBs
NCBI-GeneID:
3752
NCBI-ProteinID:
NP_004971
OMIM:
605411
HGNC:
6239
Ensembl:
ENSG00000171385
UniProt:
Q9UK17
Structure
PDB
LinkDB
All DBs
Position
1:complement(111770662..111989668)
Genome browser
AA seq
655 aa
AA seq
DB search
MAAGVAAWLPFARAAAIGWMPVANCPMPLAPADKNKRQDELIVLNVSGRRFQTWRTTLER
YPDTLLGSTEKEFFFNEDTKEYFFDRDPEVFRCVLNFYRTGKLHYPRYECISAYDDELAF
YGILPEIIGDCCYEEYKDRKRENAERLMDDNDSENNQESMPSLSFRQTMWRAFENPHTST
LALVFYYVTGFFIAVSVITNVVETVPCGTVPGSKELPCGERYSVAFFCLDTACVMIFTVE
YLLRLFAAPSRYRFIRSVMSIIDVVAIMPYYIGLVMTNNEDVSGAFVTLRVFRVFRIFKF
SRHSQGLRILGYTLKSCASELGFLLFSLTMAIIIFATVMFYAEKGSSASKFTSIPASFWY
TIVTMTTLGYGDMVPKTIAGKIFGSICSLSGVLVIALPVPVIVSNFSRIYHQNQRADKRR
AQKKARLARIRVAKTGSSNAYLHSKRNGLLNEALELTGTPEEEHMGKTTSLIESQHHHLL
HCLEKTTGLSYLVDDPLLSVRTSTIKNHEFIDEQMFEQNCMESSMQNYPSTRSPSLSSHP
GLTTTCCSRRSKKTTHLPNSNLPATRLRSMQELSTIHIQGSEQPSLTTSRSSLNLKADDG
LRPNCKTSQITTAIISIPTPPALTPEGESRPPPASPGPNTNIPSIASNVVKVSAL
NT seq
1968 nt
NT seq
+upstream
nt +downstream
nt
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