KEGG   Homo sapiens (human): 3746
Entry
3746              CDS       T01001                                 
Symbol
KCNC1, EPM7, KV3.1, KV4, NGK2
Name
(RefSeq) potassium voltage-gated channel subfamily C member 1
  KO
K04887  potassium voltage-gated channel Shaw-related subfamily C member 1
Organism
hsa  Homo sapiens (human)
Network
nt06462  Spinocerebellar ataxia
  Element
N00972  Transport of potassium
Disease
H00810  Progressive myoclonic epilepsy
Drug target
Amifampridine: D10228 D10689<JP/US>
Fampridine: D04127<US>
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3746 (KCNC1)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   3746 (KCNC1)
SSDB
Motif
Pfam: Ion_trans BTB_2 Ion_trans_2 BTB_3 PRRSV-NSP11_N
Other DBs
NCBI-GeneID: 3746
NCBI-ProteinID: NP_004967
OMIM: 176258
HGNC: 6233
Ensembl: ENSG00000129159
UniProt: P48547
Structure
LinkDB
Position
11:17734781..17783057
AA seq 511 aa
MGQGDESERIVINVGGTRHQTYRSTLRTLPGTRLAWLAEPDAHSHFDYDPRADEFFFDRH
PGVFAHILNYYRTGKLHCPADVCGPLYEEELAFWGIDETDVEPCCWMTYRQHRDAEEALD
SFGGAPLDNSADDADADGPGDSGDGEDELEMTKRLALSDSPDGRPGGFWRRWQPRIWALF
EDPYSSRYARYVAFASLFFILVSITTFCLETHERFNPIVNKTEIENVRNGTQVRYYREAE
TEAFLTYIEGVCVVWFTFEFLMRVIFCPNKVEFIKNSLNIIDFVAILPFYLEVGLSGLSS
KAAKDVLGFLRVVRFVRILRIFKLTRHFVGLRVLGHTLRASTNEFLLLIIFLALGVLIFA
TMIYYAERIGAQPNDPSASEHTHFKNIPIGFWWAVVTMTTLGYGDMYPQTWSGMLVGALC
ALAGVLTIAMPVPVIVNNFGMYYSLAMAKQKLPKKKKKHIPRPPQLGSPNYCKSVVNSPH
HSTQSDTCPLAQEEILEINRAGRKPLRGMSI
NT seq 1536 nt   +upstreamnt  +downstreamnt
atgggccaaggggacgagagcgagcgcatcgtgatcaacgtgggcggcacgcgccaccag
acgtaccgctcgaccctgcgcacgctgcccggcacgcggctcgcctggctggcggagccc
gacgcccacagccacttcgactatgacccgcgtgctgacgagttcttcttcgaccgccac
cccggcgtcttcgcgcacatcctgaactactaccgcacgggcaagctgcactgcccagcc
gacgtgtgcgggccgctctacgaggaggagctggccttctggggcatcgacgagaccgac
gtggagccctgctgctggatgacgtaccgccagcaccgcgacgccgaggaggctctggac
agcttcggcggcgctcctctggacaacagcgccgacgacgcggacgccgacggccctggc
gactcgggcgacggcgaggacgagctggagatgaccaagcgcctggcgctcagtgactcc
ccggatggccggcctggcggcttttggcgccgctggcagccgcgcatctgggcgctcttc
gaggacccgtactcgtcccgctacgcgcggtatgtggccttcgcttccctcttcttcatc
ctggtctccatcaccaccttctgcctggagacccacgagcgcttcaaccccatcgtgaac
aagacggagatcgagaacgttcgcaatggcacgcaagtgcgctactaccgggaggccgag
acggaggccttccttacctacatcgagggcgtctgtgtggtctggttcaccttcgagttc
ctcatgcgtgtcatcttctgccccaacaaggtagagttcatcaagaactcgctcaacatc
attgactttgtggccatcctgcccttctacctggaggtggggctgagcggcctgtcctcc
aaggcagccaaggacgtgctgggcttcctgcgcgtcgtccgcttcgtgcgcatcttgcgc
atctttaagctgacccgccactttgtgggcctgcgggtcctgggccacacgctccgagcc
agcaccaacgagttcctgctgctcatcatcttcctggccttgggcgtgctgatcttcgcc
accatgatctactacgccgagaggataggggcacagcccaatgaccccagcgccagtgag
cacacgcactttaagaacatccccatcggcttctggtgggccgtggtcaccatgacgacc
ctgggctatggagacatgtacccgcagacgtggtccggcatgctggtgggggctctgtgt
gcgctggcgggcgtgctcaccatcgccatgcccgtgcccgtcatcgtgaacaatttcggg
atgtattactccttagccatggctaagcagaaactaccaaagaaaaaaaagaagcatatt
ccgcggccaccgcagctgggatctcccaattattgtaaatctgtcgtaaactctccacac
cacagtactcagagtgacacatgtccgctggcccaggaagaaattttagaaattaacaga
gcaggtaggaaacctcttagaggcatgtcgatctga

KEGG   Homo sapiens (human): 3747
Entry
3747              CDS       T01001                                 
Symbol
KCNC2, DEE103, KV3.2
Name
(RefSeq) potassium voltage-gated channel subfamily C member 2
  KO
K04888  potassium voltage-gated channel Shaw-related subfamily C member 2
Organism
hsa  Homo sapiens (human)
Network
nt06462  Spinocerebellar ataxia
  Element
N00972  Transport of potassium
Disease
H00606  Early infantile epileptic encephalopathy
Drug target
Amifampridine: D10228 D10689<JP/US>
Fampridine: D04127<US>
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3747 (KCNC2)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   3747 (KCNC2)
SSDB
Motif
Pfam: Ion_trans BTB_2 Ion_trans_2 BTB_3
Other DBs
NCBI-GeneID: 3747
NCBI-ProteinID: NP_631875
OMIM: 176256
HGNC: 6234
Ensembl: ENSG00000166006
UniProt: Q96PR1
LinkDB
Position
12:complement(75040078..75209839)
AA seq 638 aa
MGKIENNERVILNVGGTRHETYRSTLKTLPGTRLALLASSEPPGDCLTTAGDKLQPSPPP
LSPPPRAPPLSPGPGGCFEGGAGNCSSRGGRASDHPGGGREFFFDRHPGVFAYVLNYYRT
GKLHCPADVCGPLFEEELAFWGIDETDVEPCCWMTYRQHRDAEEALDIFETPDLIGGDPG
DDEDLAAKRLGIEDAAGLGGPDGKSGRWRRLQPRMWALFEDPYSSRAARFIAFASLFFIL
VSITTFCLETHEAFNIVKNKTEPVINGTSVVLQYEIETDPALTYVEGVCVVWFTFEFLVR
IVFSPNKLEFIKNLLNIIDFVAILPFYLEVGLSGLSSKAAKDVLGFLRVVRFVRILRIFK
LTRHFVGLRVLGHTLRASTNEFLLLIIFLALGVLIFATMIYYAERVGAQPNDPSASEHTQ
FKNIPIGFWWAVVTMTTLGYGDMYPQTWSGMLVGALCALAGVLTIAMPVPVIVNNFGMYY
SLAMAKQKLPRKRKKHIPPAPQASSPTFCKTELNMACNSTQSDTCLGKDNRLLEHNRSVL
SGDDSTGSEPPLSPPERLPIRRSSTRDKNRRGETCFLLTTGDYTCASDGGIRKGYEKSRS
LNNIAGLAGNALRLSPVTSPYNSPCPLRRSRSPIPSIL
NT seq 1917 nt   +upstreamnt  +downstreamnt
atgggcaagatcgagaacaacgagagggtgatcctcaatgtcgggggcacccggcacgaa
acctaccgcagcaccctcaagaccctgcctggaacacgcctggcccttcttgcctcctcc
gagcccccaggcgactgcttgaccacggcgggcgacaagctgcagccgtcgccgcctcca
ctgtcgccgccgccgagagcgcccccgctgtcccccgggccaggcggctgcttcgagggc
ggcgcgggcaactgcagttcccgcggcggcagggccagcgaccatcccggtggcggccgc
gagttcttcttcgaccggcacccgggcgtcttcgcctatgtgctcaattactaccgcacc
ggcaagctgcactgccccgcagacgtgtgcgggccgctcttcgaggaggagctggccttc
tggggcatcgacgagaccgacgtggagccctgctgctggatgacctaccggcagcaccgc
gacgccgaggaggcgctggacatcttcgagacccccgacctcattggcggcgaccccggc
gacgacgaggacctggcggccaagaggctgggcatcgaggacgcggcggggctcgggggc
cccgacggcaaatctggccgctggaggaggctgcagccccgcatgtgggccctcttcgaa
gacccctactcgtccagagccgccaggtttattgcttttgcttctttattcttcatcctg
gtttcaattacaactttttgcctggaaacacatgaagctttcaatattgttaaaaacaag
acagaaccagtcatcaatggcacaagtgttgttctacagtatgaaattgaaacggatcct
gccttgacgtatgtagaaggagtgtgtgtggtgtggtttacttttgaatttttagtccgt
attgttttttcacccaataaacttgaattcatcaaaaatctcttgaatatcattgacttt
gtggccatcctacctttctacttagaggtgggactcagtgggctgtcatccaaagctgct
aaagatgtgcttggcttcctcagggtggtaaggtttgtgaggatcctgagaattttcaag
ctcacccgccattttgtaggtctgagggtgcttggacatactcttcgagctagtactaat
gaatttttgctgctgataattttcctggctctaggagttttgatatttgctaccatgatc
tactatgccgagagagtgggagctcaacctaacgacccttcagctagtgagcacacacag
ttcaaaaacattcccattgggttctggtgggctgtagtgaccatgactaccctgggttat
ggggatatgtacccccaaacatggtcaggcatgctggtgggagccctgtgtgctctggct
ggagtgctgacaatagccatgccagtgcctgtcattgtcaataattttggaatgtactac
tccttggcaatggcaaagcagaaacttccaaggaaaagaaagaagcacatccctcctgct
cctcaggcaagctcacctactttttgcaagacagaattaaatatggcctgcaatagtaca
cagagtgacacatgtctgggcaaagacaatcgacttctggaacataacagatcagtgtta
tcaggtgacgacagtacaggaagtgagccgccactatcacccccagaaaggctccccatc
agacgctctagtaccagagacaaaaacagaagaggggaaacatgtttcctactgacgaca
ggtgattacacgtgtgcttctgatggagggatcaggaaaggatatgaaaaatcccgaagc
ttaaacaacatagcgggcttggcaggcaatgctctgaggctctctccagtaacatcaccc
tacaactctccttgtcctctgaggcgctctcgatctcccatcccatctatcttgtaa

KEGG   Homo sapiens (human): 3748
Entry
3748              CDS       T01001                                 
Symbol
KCNC3, KSHIIID, KV3.3, SCA13
Name
(RefSeq) potassium voltage-gated channel subfamily C member 3
  KO
K04889  potassium voltage-gated channel Shaw-related subfamily C member 3
Organism
hsa  Homo sapiens (human)
Pathway
hsa05017  Spinocerebellar ataxia
Network
nt06462  Spinocerebellar ataxia
  Element
N00972  Transport of potassium
N00973  Mutation-inactivated KCNC3 to transport of potassium
Disease
H00063  Spinocerebellar ataxia (SCA)
Drug target
Amifampridine: D10228 D10689<JP/US>
Fampridine: D04127<US>
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09164 Neurodegenerative disease
   05017 Spinocerebellar ataxia
    3748 (KCNC3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3748 (KCNC3)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   3748 (KCNC3)
SSDB
Motif
Pfam: Ion_trans BTB_2 Ion_trans_2 BTB_3
Other DBs
NCBI-GeneID: 3748
NCBI-ProteinID: NP_004968
OMIM: 176264
HGNC: 6235
Ensembl: ENSG00000131398
UniProt: Q14003
LinkDB
Position
19:complement(50311937..50333536)
AA seq 757 aa
MLSSVCVSSFRGRQGASKQQPAPPPQPPESPPPPPLPPQQQQPAQPGPAASPAGPPAPRG
PGDRRAEPCPGLPAAAMGRHGGGGGDSGKIVINVGGVRHETYRSTLRTLPGTRLAGLTEP
EAAARFDYDPGADEFFFDRHPGVFAYVLNYYRTGKLHCPADVCGPLFEEELGFWGIDETD
VEACCWMTYRQHRDAEEALDSFEAPDPAGAANAANAAGAHDGGLDDEAGAGGGGLDGAGG
ELKRLCFQDAGGGAGGPPGGAGGAGGTWWRRWQPRVWALFEDPYSSRAARYVAFASLFFI
LISITTFCLETHEGFIHISNKTVTQASPIPGAPPENITNVEVETEPFLTYVEGVCVVWFT
FEFLMRITFCPDKVEFLKSSLNIIDCVAILPFYLEVGLSGLSSKAAKDVLGFLRVVRFVR
ILRIFKLTRHFVGLRVLGHTLRASTNEFLLLIIFLALGVLIFATMIYYAERIGADPDDIL
GSNHTYFKNIPIGFWWAVVTMTTLGYGDMYPKTWSGMLVGALCALAGVLTIAMPVPVIVN
NFGMYYSLAMAKQKLPKKKNKHIPRPPQPGSPNYCKPDPPPPPPPHPHHGSGGISPPPPI
TPPSMGVTVAGAYPAGPHTHPGLLRGGAGGLGIMGLPPLPAPGEPCPLAQEEVIEINRAD
PRPNGDPAAAALAHEDCPAIDQPAMSPEDKSPITPGSRGRYSRDRACFLLTDYAPSPDGS
IRKATGAPPLPPQDWRKPGPPSFLPDLNANAAAWISP
NT seq 2274 nt   +upstreamnt  +downstreamnt
atgctgagctcagtctgcgtctcgtccttccgcgggcgccagggggccagcaagcagcag
ccggcgccaccgccgcagccgcccgagtccccgccgccgccaccgctgccgccgcagcag
cagcagcctgcgcagcccggccccgccgcgtccccggcgggccccccggcaccccgcggg
cccggggaccggcgcgccgagccatgccccgggctgccggcggcggccatggggcggcac
ggcggcggcggtggcgacagcggcaagatcgtgatcaacgtgggcggcgtgcgccatgag
acgtaccgctcgacgctgcgcaccctgccggggacgcggctggccggcctgacggagccc
gaggcggcggcacgcttcgactacgacccgggcgccgacgagttcttctttgaccggcac
ccgggagtcttcgcgtacgtgctcaactactaccgcaccggcaagctgcactgcccagcc
gacgtgtgcgggcccctgtttgaggaggagctcggcttctggggcatcgacgagaccgac
gtggaggcctgctgctggatgacctaccggcagcatcgcgacgctgaggaggcgctcgac
tccttcgaggcgcccgaccccgcgggcgccgccaacgccgccaacgccgcaggcgcccac
gacggaggcctggacgacgaggcgggcgcgggcggcggcggcctggacggagcgggcggc
gagctcaagcgcctctgcttccaggacgcgggcggcggcgccggggggccgccagggggc
gcgggcggcgcgggcggcacatggtggcgccgctggcagccccgcgtgtgggcgctcttc
gaggacccctactcgtcgcgggctgccaggtatgtggccttcgcctccctcttcttcatc
ctcatctccatcaccaccttctgcctggaaacccatgagggcttcatccatattagcaac
aagacggtgacccaggcctccccgatccccggggcacctccggagaacatcaccaacgtg
gaggtggagacggagcccttcctgacctacgtggagggggtgtgcgtggtctggttcacc
ttcgagttcctcatgcgcatcaccttctgcccagacaaggtggagtttcttaaaagcagc
ctcaacatcatcgactgtgtggccatcctgcccttctatctcgaggtgggcctctcgggc
ctcagctccaaggccgccaaagacgtgctgggcttcctgcgggtggtccgcttcgtccgc
atcctgcgcatcttcaagctgacccggcacttcgtggggctgcgcgtgctgggacacacg
ctccgcgccagcaccaacgagttcctgctgctcatcatcttcctggccctgggggtgctc
atcttcgccaccatgatttactacgctgagcgcattggcgccgaccccgatgacatcctg
ggctccaaccacacctacttcaagaacatccccattggcttctggtgggctgtggtcacc
atgacgaccctgggctatggagacatgtaccccaagacgtggtcggggatgctggtcggg
gcgctgtgtgccctggcgggggtgctgaccatcgccatgcctgtgcccgtcattgtcaac
aactttggcatgtactattcgctggccatggccaagcagaagctgcccaagaagaagaac
aaacacatcccccggcccccgcaaccgggctcgcccaactactgcaagcctgacccaccc
ccgccacccccgccccacccgcaccacggcagcgggggcatcagcccgccgccacccatc
accccaccctccatgggggtgactgtggccggggcctacccagcggggccccacacgcac
cccgggctgctcagggggggagcgggtgggctggggatcatggggctgcctcctctgcca
gcccccggcgagccttgcccgttggctcaggaggaggtgattgagatcaaccgggcagat
cctcgccccaatggggatccggcagcagctgcgcttgcccacgaggactgcccagccatt
gaccagcctgccatgtccccggaagacaagagccccatcacgcctggaagccgtggccgc
tatagccgggaccgagcctgcttcctcctcaccgactatgccccttcccctgatggctcc
atccgaaaagccactggtgctcccccactgcccccccaagactggcgtaagccaggcccc
ccaagcttcttgcccgacctcaacgccaacgccgcggcctggatatccccctag

KEGG   Homo sapiens (human): 3749
Entry
3749              CDS       T01001                                 
Symbol
KCNC4, C1orf30, HKSHIIIC, KSHIIIC, KV3.4
Name
(RefSeq) potassium voltage-gated channel subfamily C member 4
  KO
K04890  potassium voltage-gated channel Shaw-related subfamily C member 4
Organism
hsa  Homo sapiens (human)
Network
nt06462  Spinocerebellar ataxia
  Element
N00972  Transport of potassium
Drug target
Amifampridine: D10228 D10689<JP/US>
Fampridine: D04127<US>
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    3749 (KCNC4)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Potassium channel, voltage-gated (Kv)
   3749 (KCNC4)
SSDB
Motif
Pfam: Ion_trans BTB_2 Ion_trans_2 Shal-type BTB_3 PRRSV-NSP11_N
Other DBs
NCBI-GeneID: 3749
NCBI-ProteinID: NP_004969
OMIM: 176265
HGNC: 6236
Ensembl: ENSG00000116396
UniProt: Q03721
Structure
LinkDB
Position
1:110210314..110284080
AA seq 635 aa
MISSVCVSSYRGRKSGNKPPSKTCLKEEMAKGEASEKIIINVGGTRHETYRSTLRTLPGT
RLAWLADPDGGGRPETDGGGVGSSGSSGGGGCEFFFDRHPGVFAYVLNYYRTGKLHCPAD
VCGPLFEEELTFWGIDETDVEPCCWMTYRQHRDAEEALDIFESPDGGGSGAGPSDEAGDD
ERELALQRLGPHEGGAGHGAGSGGCRGWQPRMWALFEDPYSSRAARVVAFASLFFILVSI
TTFCLETHEAFNIDRNVTEILRVGNITSVHFRREVETEPILTYIEGVCVLWFTLEFLVRI
VCCPDTLDFVKNLLNIIDFVAILPFYLEVGLSGLSSKAARDVLGFLRVVRFVRILRIFKL
TRHFVGLRVLGHTLRASTNEFLLLIIFLALGVLIFATMIYYAERIGARPSDPRGNDHTDF
KNIPIGFWWAVVTMTTLGYGDMYPKTWSGMLVGALCALAGVLTIAMPVPVIVNNFGMYYS
LAMAKQKLPKKRKKHVPRPAQLESPMYCKSEETSPRDSTCSDTSPPAREEGMIERKRADS
KQNGDANAVLSDEEGAGLTQPLASSPTPEERRALRRSTTRDRNKKAAACFLLSTGDYACA
DGSVRKGTFVLRDLPLQHSPEAACPPTAGTLFLPH
NT seq 1908 nt   +upstreamnt  +downstreamnt
atgatcagctcggtgtgtgtctcctcctaccgcgggcgcaagtcggggaacaagcctccg
tccaaaacatgtctgaaggaggagatggccaagggcgaggcgtcggagaagatcatcatc
aacgtgggcggcacgcgacatgagacctaccgcagcaccctgcgcaccctaccgggaacc
cgcctcgcctggctggccgaccccgacggcgggggccggcccgagaccgatggcggcggt
gtgggtagcagcggcagcagcggcggcgggggctgcgagttcttcttcgacaggcacccg
ggcgtcttcgcctacgtgctcaactactaccgcaccggcaagctgcactgccccgcggac
gtgtgcgggccgctcttcgaagaggagctcaccttctggggcatcgacgagaccgacgtg
gaaccctgctgctggatgacctaccggcagcaccgcgacgccgaggaggcgctcgacatc
ttcgagagcccggacggaggcggcagcggcgcggggcccagcgacgaggccggcgacgat
gagcgggagctggccctgcagcgactgggcccccacgagggaggcgcgggccatggcgcc
gggtctgggggctgccgcggctggcagccccgcatgtgggcgctcttcgaggatccctac
tcctcccgggccgctagggtagtggcctttgcctctctcttcttcatcctggtctccatc
accactttctgcctggagacccatgaggcctttaatatcgaccgcaacgtgacagagatc
ctccgcgtagggaacatcaccagcgtgcacttccggcgggaggtagagacagagcccatc
ctgacctacatcgagggcgtatgtgtgctgtggttcacactggagttcctggtgcgcatc
gtgtgctgccccgacacgctggacttcgtcaagaacctgctcaacatcatcgactttgtg
gccatcctgcccttctacctggaggtggggctgagcggcctgtcatccaaggcggcccgc
gacgtgctgggcttcctgcgcgtggtgcgcttcgtgcgcatcctgcgtatcttcaagctc
acacgccacttcgtggggctacgcgtgctgggccacaccctgagggccagcaccaatgag
ttcctgctgcttatcatcttcctggccctgggtgtgctcatctttgccaccatgatctac
tacgctgagcgcattggggccaggccctccgaccctcggggtaatgaccacaccgacttc
aagaacatccccattggcttctggtgggctgtggtcaccatgacgacactgggctacgga
gacatgtaccccaagacgtggtcaggcatgctggtaggggcactgtgtgcactggctggc
gtgctcaccatcgccatgccggtgcctgtcatcgtcaacaacttcggcatgtactactcc
ctggccatggccaagcagaagctgcccaagaaacggaagaagcacgtgccacggccggcg
cagctggagtcacccatgtactgcaagtctgaggagacttccccccgggacagcacctgc
agtgataccagcccccctgcccgggaagagggtatgatcgagaggaaacgggcagactct
aagcagaatggcgatgccaacgcagtgctgtctgatgaggagggagctggcctcacccaa
cccctggcctcctccccgacccccgaggagcgccgggccctgcgacgctccaccactcga
gacagaaacaagaaggcagctgcctgcttcctgctcagcactggggactatgcctgcgcc
gatggtagtgtccggaaaggcacattcgtcctccgtgaccttccccttcagcattcacct
gaggctgcatgccctccaactgctgggactctgttcctgccacattga

DBGET integrated database retrieval system