Type | Description |
---|---|
Definition | potassium voltage-gated channel subfamily A member 1 |
Date | Results | Publications |
---|---|---|
2021-02-27 13:48:00 | A Common Kinetic Property of Mutations Linked to Episodic Ataxia Type 1 Studied in the Shaker Kv Channel. | 33066705 |
2021-02-06 13:56:00 | Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia. | 31586945 |
2021-01-23 12:57:00 | Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity. | 32316562 |
2020-09-12 16:05:00 | Isoform-Selective KCNA1 Openers Built from Glycine. | 32217768 |
2020-07-18 12:31:00 | Kv1.1 is important for neural control of the heart and that Kcna1 deletion leads to cardiac dysfunction that appears to be brain-driven. [review] | 31250689 |
Type | IDs |
---|---|
Synonymous | AEMK, EA1, HBK1, HUK1, KV1.1, MBK1, MK1, RBK1 |
Gene |
UniProtKB-ID:
KCNA1_HUMAN
UniprotKB:
Q09470
UniParc:
UPI000013C8E0
EMBL:
L02750,
BC101733,
CH471116,
AC006063,
BC112180
Ensembl:
ENSG00000111262
KO:
hsa:3736
|
Nucleutide sequences |
EMBL-CDS:
AAA36139.1,
AAI01734.1,
AAI12181.1,
EAW88833.1
Ensembl_TRS:
ENST00000382545
|
Protein sequencees |
Ensembl_PRO:
ENSP00000371985
RefSeq:
NP_000208.2
|
Others |
UniRef100:
UniRef100_Q09470
UniRef90:
UniRef90_Q09470
UniRef50:
UniRef50_Q09470
UniGene:
Hs.416139
CCDS:
CCDS8535.1
|
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Refseq |
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