Type | Description |
---|---|
Definition | potassium two pore domain channel subfamily K member 9 |
Date | Results | Publications |
---|---|---|
2020-04-18 10:12:00 | cell migration and invasion are reduced after knocking down TASK-3 in these cell lines. The present study highlights TASK-3 as a key protein involved in migration and cell survival in gastric cancer and corroborates its potential as a therapeutic target for gastric cancer treatment. | 31810225 |
2018-09-08 11:43:00 | observations implicate TASK-3 as a critical factor in cell cycle progression and corroborate its potential as a therapeutic target in breast cancer treatment. | 29596383 |
2018-06-09 10:03:00 | point mutations in DLK1 and KCNK9 at least do not seem to be a common cause of central precocious puberty in girls. | 28672280 |
2017-10-28 11:26:00 | In conclusion, we have identified the first selective activator of the two-pore domain potassium channel TASK3. | 28882594 |
2017-10-21 10:25:00 | KCNK9 imprinting syndrome is a rare cause of intellectual disability, congenital hypotonia, palatal abnormalities, and occasional seizures. | 27151206 |
Type | IDs |
---|---|
Synonymous | K2p9.1, KT3.2, TASK-3, TASK3 |
Gene |
UniProtKB-ID:
KCNK9_HUMAN,
A0A024R9H3_HUMAN
UniprotKB:
Q9NPC2,
A0A024R9H3
UniParc:
UPI000000D8AC
EMBL:
CH471060,
BC075079,
AF257080,
AY190605,
AF212829,
BC112065,
BC112063,
AF279809,
BC075080,
AF248241
Ensembl:
ENSG00000169427
KO:
hsa:51305
|
Nucleutide sequences |
EMBL-CDS:
AAH75080.1,
AAI12066.1,
AAF63708.1,
AAG33126.1,
AAI12064.1,
AAF85982.1,
AAH75079.1,
AAO38739.1,
AAG31730.1,
EAW92198.1,
EAW92197.1
Gene_ORFName:
hCG_22533
Ensembl_TRS:
ENST00000520439,
ENST00000648164,
ENST00000303015,
ENST00000522317,
ENST00000650269
|
Protein sequencees |
Ensembl_PRO:
ENSP00000302166,
ENSP00000496915,
ENSP00000429847,
ENSP00000498198,
ENSP00000430676
RefSeq:
XP_011515405.1,
XP_016869020.1,
XP_011515404.1,
XP_011515403.1,
XP_016869019.1,
NP_001269463.1
|
Others |
UniRef100:
UniRef100_Q9NPC2
UniRef90:
UniRef90_Q9NPC2
UniRef50:
UniRef50_Q9NPC2
UniGene:
Hs.493037
CCDS:
CCDS6377.1
|
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