2. Gene
  3. Kcnj13 - potassium inwardly-rectifying channel, subfamily J, member 13 Gene

Kcnj13 - potassium inwardly-rectifying channel, subfamily J, member 13 Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Rattus norvegicus

Also known as Kir7.1

Gene ID: 94341 | Gene type: protein coding

About Kcnj13

Summary

Predicted to enable inward rectifier Potassium Channel activity. Predicted to be involved in potassium ion import across plasma membrane and regulation of ion transmembrane transport. Predicted to be integral component of membrane. Predicted to be active in plasma membrane. Human ortholog(s) of this gene implicated in Leber congenital amaurosis 16 and snowflake vitreoretinal degeneration. Orthologous to human KCNJ13 (potassium inwardly rectifying channel subfamily J member 13). [provided by Alliance of Genome Resources, Apr 2022]

Kcnj13 Products(1)

mRNA Protein Name
NM_053608.2 NP_446060.1 inward rectifier potassium channel 13
Protein Preferred Names Protein Names

inward rectifier potassium channel 13

inward rectifier K(+) channel Kir7.1

potassium channel, inwardly rectifying subfamily J member 13

potassium voltage-gated channel subfamily J member 13

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS07140 KCNJ13 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Kcnj13 NCBI NCBI:3769