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si:ch211-214b16.3 - si:ch211-214b16.3

Predicted to be involved in intracellular signal transduction. Human ortholog(s) of this gene implicated in CINCA Syndrome; Muckle-Wells syndrome; autosomal dominant nonsyndromic deafness 34; familial cold autoinflammatory syndrome (multiple); and urticaria. Orthologous to several human genes including NLRP12 (NLR family pyrin domain containing 12); NLRP13 (NLR family pyrin domain containing 13); and NLRP14 (NLR family pyrin domain containing 14). [provided by Alliance of Genome Resources, Dec 2024]

Genes similar to si:ch211-214b16.3

NCBI Orthologs

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Species Gene Architecture aa