MYO16 (Entrez ID: 23026)

Entrez Gene ID	23026
Official Gene Symbol	MYO16 (GeneCards)
Full name	myosin XVI
Location	13q33.3
Other ids	MIM : 615479 HGNC : HGNC:29822 Ensembl : ENSG00000041515
Other names	MYR8, MYAP3, NYAP3, Myo16b, PPP1R107
Summary	This gene encodes an unconventional myosin protein. The encoded protein has been proposed to act as a serine/threonine phosphatase-1 targeting or regulatory subunit. Studies in a rat cell line suggest that this protein may regulate cell cycle progression. A variant within this gene may be associated with susceptibility to schizophrenia and elevated expression of this gene has been observed in the frontal cortex of human schizophrenia patients. [provided by RefSeq, Mar 2017]

Variants

Found 16 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
17153	23026	MYO16	13	109447822	109447822	Asymptomatic	HiSeq X Ten
17232	23026	MYO16	13	109531879	109531879	Asymptomatic	HiSeq X Ten
17290	23026	MYO16	13	109657414	109657414	Asymptomatic	HiSeq X Ten
17357	23026	MYO16	13	109588340	109588340	Asymptomatic	HiSeq X Ten
17408	23026	MYO16	13	109435484	109435484	Asymptomatic	HiSeq X Ten
17447	23026	MYO16	13	109407689	109407689	Asymptomatic	HiSeq X Ten
17647	23026	MYO16	13	109736141	109736141	Asymptomatic	HiSeq X Ten
17659	23026	MYO16	13	109504986	109504986	Asymptomatic	HiSeq X Ten
17660	23026	MYO16	13	109748279	109748279	Asymptomatic	HiSeq X Ten
17776	23026	MYO16	13	109833951	109833951	Asymptomatic	HiSeq X Ten
17777	23026	MYO16	13	109907462	109907462	Asymptomatic	HiSeq X Ten
17806	23026	MYO16	13	109277640	109277640	Asymptomatic	HiSeq X Ten
17899	23026	MYO16	13	109762667	109762667	Cockayne syndrome	HiSeq X Ten
17938	23026	MYO16	13	109799447	109799447	Xeroderma Pigmentosum	HiSeq X Ten
17968	23026	MYO16	13	109326410	109326410	Xeroderma Pigmentosum	HiSeq X Ten
29160	23026	MYO16	13	109817311	109817311	Autism Spectrum Disorders	HiSeq X Ten PASM