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3783 KCNN4

3783

KCNN4

potassium calcium-activated channel subfamily N member 4

protein-coding

Homo sapiens

基因描述

Type Description
Definition potassium calcium-activated channel subfamily N member 4

研究结论

Date Results Publications
2020-07-25 12:19:00 In KCNN4-related disease, the main symptoms were more severe anemia, hemolysis and iron overload, with no clear sign of red cell dehydration; therefore, this disorder would be better described as a 'Gardos channelopathy'. 30655378
2020-06-06 12:14:00 High KCa3.1 Expression is associated with Active Ulcerative Colitis. 31141130
2020-03-28 10:06:00 Chronic KCNN4-driven red cell dehydration and intracellular cation imbalance can lead to reduced KCNN4 activity in hereditary xerocytosis and wild type red cells. 31091145
2019-12-14 12:25:00 Data demonstrate that IKCa and SK1 subunits prefer to form heteromeric channels when coexpressed in a heterologous system that will alter their responsiveness to pharmacological tools typically used to define their expression pattern. 31048549
2019-11-02 11:32:00 Study found that the expression of KCa3.1 was significantly elevated in poorly differentiated hepatocellular carcinoma (HCC) tissues and could promote cell proliferation, migration, and invasion. Mechanistically, KCa3.1 promoted cell cycle progression and migration and invasion of HCC cells by SKP2 to trigger the degradation of p21 and p27 and targeting RELN to induce epithelial-mesenchymal transition. 30628729

名称对应

Type IDs
Synonymous DHS2, IK, IK1, IKCA1, KCA4, KCa3.1, SK4, hIKCa1, hKCa4, hSK4
Gene
UniProtKB-ID: KCNN4_HUMAN
UniprotKB: O15554
UniParc: UPI0000000DF3
EMBL: AF053403, BT007426, AF000972, AF395661, AF305733, AF305731, CH471126, AF022797, BC015337, AF305732, AF305735, AF033021, AF305734, AF022150
Ensembl: ENSG00000104783
KO: hsa:3783
Nucleutide sequences
EMBL-CDS: AAP36094.1, AAC36804.1, AAB82739.1, AAC51913.1, AAC23541.1, AAH15337.1, AAC35281.1, AAG26917.1, EAW57230.1, AAK81862.1
Ensembl_TRS: ENST00000648319
Protein sequencees
Ensembl_PRO: ENSP00000496939
RefSeq: XP_005258939.1, NP_002241.1, XP_005258940.1
Others
UniRef100: UniRef100_O15554
UniRef90: UniRef90_O15554
UniRef50: UniRef50_O15554
UniGene: Hs.10082
CCDS: CCDS12630.1

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