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kcnj1a.1


Official Full Name
potassium inwardly rectifying channel subfamily J member 1a, tandem duplicate 1
Organism
Danio rerio
Gene ID
386933
Background
Enables inward rectifier potassium channel activity. Predicted to be involved in potassium ion import across plasma membrane and regulation of monoatomic ion transmembrane transport. Predicted to act upstream of or within monoatomic ion transmembrane transport and potassium ion transport. Predicted to be located in membrane. Predicted to be part of monoatomic ion channel complex. Predicted to be active in plasma membrane. Is expressed in several structures, including gill; integument; ionocyte; pharyngeal arch; and pronephric duct. Human ortholog(s) of this gene implicated in Bartter disease type 2. Orthologous to human KCNJ1 (potassium inwardly rectifying channel subfamily J member 1). [provided by Alliance of Genome Resources, Feb 2025]
Synonyms
kcnj1; romk2; zgc:63534; wu:fl37c05

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