KCNN3 (potassium calcium-activated channel subfamily N member 3)

2010-02-01  

Identity

HGNC
LOCATION
1q21.3
LOCUSID
ALIAS
KCa2.3,SK3,SKCA3,ZLS3,hSK3
FUSION GENES

Other Information

Locus ID:

NCBI: 3782
MIM: 602983
HGNC: 6292
Ensembl: ENSG00000143603

Variants:

dbSNP: 3782
ClinVar: 3782
TCGA: ENSG00000143603
COSMIC: KCNN3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000143603ENST00000271915Q9UGI6
ENSG00000143603ENST00000358505Q9UGI6
ENSG00000143603ENST00000361147Q9UGI6
ENSG00000143603ENST00000618040A0A087WYJ0

Expression (GTEx)

0
5
10
15
20

Pathways

PathwaySourceExternal ID
Insulin secretionKEGGhsa04911
Neuronal SystemREACTOMER-HSA-112316
Potassium ChannelsREACTOMER-HSA-1296071
Ca2+ activated K+ channelsREACTOMER-HSA-1296052

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
365029182023Preferential formation of human heteromeric SK2:SK3 channels limits homomeric SK channel assembly and function.2
365029182023Preferential formation of human heteromeric SK2:SK3 channels limits homomeric SK channel assembly and function.2
354883062022The role of SK3 in progesterone-induced inhibition of human fallopian tubal contraction.2
354883062022The role of SK3 in progesterone-induced inhibition of human fallopian tubal contraction.2
333100412021HDAC2-dependent remodeling of K(Ca)2.2 (KCNN2) and K(Ca)2.3 (KCNN3) K(+) channels in atrial fibrillation with concomitant heart failure.7
335942612021Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K(+) channelopathies.16
333100412021HDAC2-dependent remodeling of K(Ca)2.2 (KCNN2) and K(Ca)2.3 (KCNN3) K(+) channels in atrial fibrillation with concomitant heart failure.7
335942612021Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K(+) channelopathies.16
326407382020Hypoxia Promotes Prostate Cancer Aggressiveness by Upregulating EMT-Activator Zeb1 and SK3 Channel Expression.12
326407382020Hypoxia Promotes Prostate Cancer Aggressiveness by Upregulating EMT-Activator Zeb1 and SK3 Channel Expression.12
309225692019Role of SK channel activation in determining the action potential configuration in freshly isolated human atrial myocytes from the SKArF study.6
311552822019Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca(2+)-Activated K(+) Channel SK3 Cause Zimmermann-Laband Syndrome.26
314862522019Liability of the voltage-gated potassium channel KCNN3 repeat polymorphism to acute oxaliplatin-induced peripheral neurotoxicity.5
309225692019Role of SK channel activation in determining the action potential configuration in freshly isolated human atrial myocytes from the SKArF study.6
311552822019Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca(2+)-Activated K(+) Channel SK3 Cause Zimmermann-Laband Syndrome.26

Citation

Dessen P

KCNN3 (potassium calcium-activated channel subfamily N member 3)

Atlas Genet Cytogenet Oncol Haematol. 2010-02-01

Online version: http://atlasgeneticsoncology.org/gene/51331/css/favicon/js/lib/zoomerang.js