Kcnq1 - potassium voltage-gated channel, subfamily Q, member 1 Gene
Also Known as Kcna9; KVLQT1
生物種: Mus musculus
Summary
Enables voltage-gated Potassium Channel activity. Involved in several processes, including animal organ development; inorganic ion homeostasis; and regulation of heart contraction. Acts upstream of or within circulatory system development; negative regulation of gene expression; and regulation of gene expression by genetic imprinting. Located in apical part of cell; neuron projection; and transport vesicle. Part of voltage-gated Potassium Channel complex. Is active in several cellular components, including apical plasma membrane; basolateral part of cell; and ciliary base. Is expressed in several structures, including alimentary system; extraembryonic component; heart; hemolymphoid system gland; and reproductive system. Used to study Jervell-Lange Nielsen syndrome and long QT syndrome 1. Human ortholog(s) of this gene implicated in heart conduction disease (multiple) and long QT syndrome (multiple). Orthologous to human KCNQ1 (potassium voltage-gated channel subfamily Q member 1). [provided by Alliance of Genome Resources, Apr 2022]
Kcnq1 Products (3)
| mRNA | Protein | Name |
|---|---|---|
| NM_001412611.1 | NP_001399540.1 | potassium voltage-gated channel subfamily KQT member 1 isoform 2 |
| NM_001412612.1 | NP_001399541.1 | potassium voltage-gated channel subfamily KQT member 1 isoform 3 |
| NM_008434.3 | NP_032460.2 | potassium voltage-gated channel subfamily KQT member 1 isoform 1 |
| Molecular Function GO Annotation | Evidence | 参考文献 | 由来 |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
24595108 | MGI |
| enables voltage-gated potassium channel activity |
IDA
IDA: Inferred from direct assay
|
8900282 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
potassium voltage-gated channel subfamily KQT member 1 |
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