NLRC2)

Editor(s): Suzanne LESAGE

General web sites
LRG	LRG_177
DNA	NC_000016.10 GRCh38.p13	ENSG00000167207 GRCh38.p13
	NC_000016.9GRCh37.p13	ENSG00000167207 GRCh37.p13
	NG_007508.1
mRNA	NM_022162.3
CCDS	CCDS10746.1
Protein	NP_071445.1
NCBI Gene	64127
OMIM Gene	605956
OMIM Disease	186580 266600
Nomenclature	HGNC

PubMed of the initial paper: Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Hugot JP & al CARD15 mutations in Blau syndrome. Miceli-Richard C & al Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome. Kanazawa N & al
Other links: MAP VIEW ORPHANET: Orphan disease database