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Official Full Name
potassium inwardly-rectifying channel, subfamily J, member 13
This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.
KCNJ13; potassium inwardly-rectifying channel, subfamily J, member 13; inward rectifier potassium channel 13; Kir1.4; Kir7.1; inwardly rectifying subfamily J member 13; Inward rectifier K(+) channel Kir7.1; IRK13_HUMAN; Potassium channel; Potassium inwardly rectifying channelsubfamily Jmember 13; SVD; LCA16; MGC33328; jag; obe; jaguar; obelix; inwardly rectifying potassium channel 7.1

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