Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	MYOSIN VA
Synonyms	GRISCELLI SYNDROME, TYPE 3
ID	http://purl.bioontology.org/ontology/OMIM/160777
altLabel	GRISCELLI SYNDROME, TYPE 3 DILUTE, MOUSE, HOMOLOG OF MYO5A MYH12 GRISCELLI SYNDROME, TYPE 1 MYOSIN, HEAVY CHAIN 12 MYO5 MYOXIN
cui	C1859194 C1836573 C1417565
Gene Locus	15q21
Gene Symbol	MYO5A GS1 MYH12
Has allelic variant	http://purl.bioontology.org/ontology/OMIM/160777.0004 http://purl.bioontology.org/ontology/OMIM/160777.0003 http://purl.bioontology.org/ontology/OMIM/160777.0002
MIMTYPEMEANING	Gene with known sequence
notation	160777
OMIM Entry Type	1
OMIM MimType Value	star
prefLabel	MYOSIN VA
tui	T028 T047

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/PR_000010865	Protein Ontology	LOOM
http://purl.bioontology.org/ontology/MESH/C537301	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/C537303	Medical Subject Headings	CUI