Homo sapiens (human): 169522
Help
Entry
169522 CDS
T01001
Symbol
KCNV2, CDSRR, KV11.1, Kv8.2, RCD3B
Name
(RefSeq) potassium voltage-gated channel modifier subfamily V member 2
KO
K04935
potassium channel subfamily V member 2
Organism
hsa
Homo sapiens (human)
Disease
H00481
Cone-rod dystrophy and cone dystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
hsa04040
]
169522 (KCNV2)
Ion channels [BR:
hsa04040
]
Voltage-gated cation channels
Potassium channel, voltage-gated (Kv)
169522 (KCNV2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ion_trans
BTB_2
Ion_trans_2
PKD_channel
Motif
Other DBs
NCBI-GeneID:
169522
NCBI-ProteinID:
NP_598004
OMIM:
607604
HGNC:
19698
Ensembl:
ENSG00000168263
UniProt:
Q8TDN2
LinkDB
All DBs
Position
9:2717510..2730037
Genome browser
AA seq
545 aa
AA seq
DB search
MLKQSERRRSWSYRPWNTTENEGSQHRRSICSLGARSGSQASIHGWTEGNYNYYIEEDED
GEEEDQWKDDLAEEDQQAGEVTTAKPEGPSDPPALLSTLNVNVGGHSYQLDYCELAGFPK
TRLGRLATSTSRSRQLSLCDDYEEQTDEYFFDRDPAVFQLVYNFYLSGVLLVLDGLCPRR
FLEELGYWGVRLKYTPRCCRICFEERRDELSERLKIQHELRAQAQVEEAEELFRDMRFYG
PQRRRLWNLMEKPFSSVAAKAIGVASSTFVLVSVVALALNTVEEMQQHSGQGEGGPDLRP
ILEHVEMLCMGFFTLEYLLRLASTPDLRRFARSALNLVDLVAILPLYLQLLLECFTGEGH
QRGQTVGSVGKVGQVLRVMRLMRIFRILKLARHSTGLRAFGFTLRQCYQQVGCLLLFIAM
GIFTFSAAVYSVEHDVPSTNFTTIPHSWWWAAVSISTVGYGDMYPETHLGRFFAFLCIAF
GIILNGMPISILYNKFSDYYSKLKAYEYTTIRRERGEVNFMQRARKKIAECLLGSNPQLT
PRQEN
NT seq
1638 nt
NT seq
+upstream
nt +downstream
nt
atgctcaaacagagtgagaggagacggtcctggagctacaggccctggaacacgacggag
aatgagggcagccaacaccgcaggagcatttgctccctgggtgcccgttccggctcccag
gccagcatccacggctggacagagggcaactataactactacatcgaggaagacgaagac
ggcgaggaggaggaccagtggaaggacgacctggcagaagaggaccagcaggcaggggag
gtcaccaccgccaagcccgagggccccagcgaccctccggccctgctgtccacgctgaat
gtgaacgtgggtggccacagctaccagctggactactgcgagctggccggcttccccaag
acgcgcctaggtcgcctggccacctccaccagccgcagccgccagctaagcctgtgcgac
gactacgaggagcagacagacgaatacttcttcgaccgcgacccggccgtcttccagctg
gtctacaatttctacctgtccggggtgctgctggtgctcgacgggctgtgtccgcgccgc
ttcctggaggagctgggctactggggcgtgcggctcaagtacacgccacgctgctgccgc
atctgcttcgaggagcggcgcgacgagctgagcgaacggctcaagatccagcacgagctg
cgcgcgcaggcgcaggtcgaggaggcggaggaactcttccgcgacatgcgcttctacggc
ccgcagcggcgccgcctctggaacctcatggagaagccattctcctcggtggccgccaag
gccatcggggtggcctccagcaccttcgtgctcgtctccgtggtggcgctggcgctcaac
accgtggaggagatgcagcagcactcggggcagggcgagggcggcccagacctgcggccc
atcctggagcacgtggagatgctgtgcatgggcttcttcacgctcgagtacctgctgcgc
ctagcctccacgcccgacctgaggcgcttcgcgcgcagcgccctcaacctggtggacctg
gtggccatcctgccgctctaccttcagctgctgctcgagtgcttcacgggcgagggccac
caacgcggccagacggtgggcagcgtgggtaaggtgggtcaggtgttgcgcgtcatgcgc
ctcatgcgcatcttccgcatcctcaagctggcgcgccactccaccggactgcgtgccttc
ggcttcacgctgcgccagtgctaccagcaggtgggctgcctgctgctcttcatcgccatg
ggcatcttcactttctctgcggctgtctactctgtggagcacgatgtgcccagcaccaac
ttcactaccatcccccactcctggtggtgggccgcggtgagcatctccaccgtgggctac
ggagacatgtacccagagacccacctgggcaggttttttgccttcctctgcattgctttt
gggatcattctcaacgggatgcccatttccatcctctacaacaagttttctgattactac
agcaagctgaaggcttatgagtataccaccatacgcagggagaggggagaggtgaacttc
atgcagagagccagaaagaagatagctgagtgtttgcttggaagcaacccacagctcacc
ccaagacaagagaattag
DBGET
integrated database retrieval system
