Gene and Protein Information
Species	TM	AA	Chromosomal Location	Gene Symbol	Gene Name	Reference
Human	-	1200	19q13.43	NLRP5	NLR family pyrin domain containing 5
Mouse	-	1163	7 10.22 cM	Nlrp5	NLR family, pyrin domain containing 5
Rat	-	-	1q12	Nlrp5	NLR family

Previous and Unofficial Names

CLR19.8 | MATER | NALP5 | PAN11 | PYPAF8 | NACHT, leucine rich repeat and PYD containing 5 | NLR family, pyrin domain containing 5 | NLR family

Database Links
Alphafold	P59047 (Hs), Q9R1M5 (Mm)
Ensembl Gene	ENSG00000171487 (Hs), ENSMUSG00000015721 (Mm), ENSRNOG00000022994 (Rn)
Entrez Gene	126206 (Hs), 23968 (Mm), 308325 (Rn)
Human Protein Atlas	ENSG00000171487 (Hs)
KEGG Gene	hsa:126206 (Hs), mmu:23968 (Mm), rno:308325 (Rn)
OMIM	609658 (Hs)
Pharos	P59047 (Hs)
UniProtKB	P59047 (Hs), Q9R1M5 (Mm)
Wikipedia	NLRP5 (Hs)

Physiological Functions Comments

Involved in embryonic development

Clinically-Relevant Mutations and Pathophysiology
Disease:  Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia; APS1 Synonyms: Autoimmune polyendocrine syndrome type 1 [Disease Ontology: DOID:0050167] Disease Ontology: DOID:0050167 OMIM: 240300