MYO10 (Entrez ID: 4651)

Entrez Gene ID	4651
Official Gene Symbol	MYO10 (GeneCards)
Full name	myosin X
Location	5p15.1
Other ids	Vega : OTTHUMG00000161822 MIM : 601481 HGNC : HGNC:7593 Ensembl : ENSG00000145555
Other names	None
Summary	This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-10 (MYH10). Unconventional myosins contain the basic domains of conventional myosins and are further distinguished from class members by their tail domains. This gene functions as an actin-based molecular motor and plays a role in integration of F-actin and microtubule cytoskeletons during meiosis. [provided by RefSeq, Dec 2011]

Variants

Found 10 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
7575	4651	MYO10	5	16896726	16896726	Asymptomatic	HiSeq 2000
7622	4651	MYO10	5	16926111	16926111	Asymptomatic	HiSeq 2000 HiSeq X Ten
7623	4651	MYO10	5	16933278	16933278	Asymptomatic	HiSeq 2000 HiSeq X Ten
7874	4651	MYO10	5	17002689	17002689	Asymptomatic	HiSeq 2000 HiSeq X Ten
7897	4651	MYO10	5	17057041	17057041	Asymptomatic	HiSeq 2000 HiSeq X Ten
8121	4651	MYO10	5	16984739	16984739	Asymptomatic	HiSeq 2000 HiSeq X Ten
8517	4651	MYO10	5	17045422	17045422	Asymptomatic	HiSeq 2000 HiSeq X Ten
8604	4651	MYO10	5	16920114	16920114	Cockayne syndrome	HiSeq 2000 HiSeq X Ten
8723	4651	MYO10	5	16938101	16938101	Cockayne syndrome	HiSeq 2000 HiSeq X Ten
8842	4651	MYO10	5	16686972	16686972	Xeroderma Pigmentosum	HiSeq 2000 HiSeq X Ten