LRMDA (Entrez ID: 83938)

Entrez Gene ID	83938
Official Gene Symbol	LRMDA (GeneCards)
Full name	leucine rich melanocyte differentiation associated
Location	10q22.2-q22.3
Other ids	Vega : OTTHUMG00000018532 MIM : 614537 HGNC : HGNC:23405 Ensembl : ENSG00000148655
Other names	CDA017, C10orf11
Summary	This gene encodes a leucine-rich repeat protein. The encoded protein is thought to play a role in melanocyte differentiation. Mutations in this gene have been associated with autosomal recessive oculocutaneous albinism 7 (OCA7). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]

Variants

Found 13 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
13881	83938	C10orf11	10	77743218	77743218	Asymptomatic	HiSeq X Ten
14075	83938	C10orf11	10	78457684	78457684	Asymptomatic	HiSeq X Ten
14150	83938	C10orf11	10	78274282	78274282	Asymptomatic	HiSeq X Ten
14241	83938	C10orf11	10	77769245	77769245	Asymptomatic	HiSeq X Ten
14263	83938	C10orf11	10	77896721	77896721	Asymptomatic	HiSeq X Ten
14296	83938	C10orf11	10	78039865	78039865	Asymptomatic	HiSeq X Ten
14435	83938	C10orf11	10	78321431	78321431	Asymptomatic	HiSeq X Ten
14631	83938	C10orf11	10	77746789	77746789	Asymptomatic	HiSeq X Ten
14656	83938	C10orf11	10	78296041	78296041	Asymptomatic	HiSeq X Ten
14743	83938	C10orf11	10	78476012	78476012	Cockayne syndrome	HiSeq X Ten
14870	83938	C10orf11	10	78182040	78182040	Xeroderma Pigmentosum	HiSeq X Ten
27020	83938	C10orf11	10	78474530	78474530	Asymptomatic	HiSeq X Ten Single cell Sequencing Cell cloning
27128	83938	C10orf11	10	78314392	78314392	Asymptomatic	HiSeq X Ten Single cell Sequencing Cell cloning