Homo sapiens (human): 9992
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Entry
9992 CDS
T01001
Symbol
KCNE2, ATFB4, LQT5, LQT6, MIRP1
Name
(RefSeq) potassium voltage-gated channel subfamily E regulatory subunit 2
KO
K04896
potassium voltage-gated channel Isk-related subfamily E member 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04971
Gastric acid secretion
Disease
H00720
Long QT syndrome
H00731
Atrial fibrillation
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09154 Digestive system
04971 Gastric acid secretion
9992 (KCNE2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
hsa04040
]
9992 (KCNE2)
Ion channels [BR:
hsa04040
]
Voltage-gated cation channels
Potassium channel, voltage-gated (Kv)
9992 (KCNE2)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ISK_Channel
SLC52_ribofla_tr
SID-1_RNA_chan
Motif
Other DBs
NCBI-GeneID:
9992
NCBI-ProteinID:
NP_751951
OMIM:
603796
HGNC:
6242
Ensembl:
ENSG00000159197
UniProt:
Q9Y6J6
Structure
PDB
PDBj
LinkDB
All DBs
Position
21:34364006..34371381
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AA seq
123 aa
AA seq
DB search
MSTLSNFTQTLEDVFRRIFITYMDNWRQNTTAEQEALQAKVDAENFYYVILYLMVMIGMF
SFIIVAILVSTVKSKRREHSNDPYHQYIVEDWQEKYKSQILNLEESKATIHENIGAAGFK
MSP
NT seq
372 nt
NT seq
+upstream
nt +downstream
nt
atgtctactttatccaatttcacacagacgctggaagacgtcttccgaaggatttttatt
acttatatggacaattggcgccagaacacaacagctgagcaagaggccctccaagccaaa
gttgatgctgagaacttctactatgtcatcctgtacctcatggtgatgattggaatgttc
tctttcatcatcgtggccatcctggtgagcactgtgaaatccaagagacgggaacactcc
aatgacccctaccaccagtacattgtagaggactggcaggaaaagtacaagagccaaatc
ttgaatctagaagaatcgaaggccaccatccatgagaacattggtgcggctgggttcaaa
atgtccccctga
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integrated database retrieval system
