Kcnq4 - potassium voltage-gated channel, subfamily Q, member 4 Gene
Species: Mus musculus
Summary
Enables voltage-gated Potassium Channel activity. Acts upstream of or within inner ear morphogenesis; potassium ion transport; and sensory perception of sound. Predicted to be located in plasma membrane. Predicted to be part of voltage-gated Potassium Channel complex. Predicted to be integral component of membrane. Is expressed in heart; utricle; and utricle epithelium. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 2A and sensorineural hearing loss. Orthologous to human KCNQ4 (potassium voltage-gated channel subfamily Q member 4). [provided by Alliance of Genome Resources, Apr 2022]
Kcnq4 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001081142.3 | NP_001074611.1 | potassium voltage-gated channel subfamily KQT member 4 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables voltage-gated potassium channel activity |
IMP
IMP: Inferred from mutant phenotype
|
16437162 | MGI |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| acts upstream of or within inner ear morphogenesis |
IMP
IMP: Inferred from mutant phenotype
|
16437162 | MGI |
| acts upstream of or within potassium ion transport |
IMP
IMP: Inferred from mutant phenotype
|
16437162 | MGI |
| acts upstream of or within sensory perception of sound |
IMP
IMP: Inferred from mutant phenotype
|
16437162 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
potassium voltage-gated channel subfamily KQT member 4 |
|
|