Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	PROMININ 1
Synonyms	STARGARDT DISEASE 4
ID	http://purl.bioontology.org/ontology/OMIM/604365
altLabel	STARGARDT DISEASE 4 RETINITIS PIGMENTOSA 41 PROMININ, MOUSE, HOMOLOG-LIKE 1 MACULAR DYSTROPHY, RETINAL, 2 PROML1 PROM1 CONE-ROD DYSTROPHY 12 AC133 CD133 CD133 ANTIGEN
cui	C2677516 C2675210 C1418946 C0339512 C1863534
Gene Locus	4p15.3
Gene Symbol	MCDR2 RP41 PROML1 PROM1 AC133 STGD4 CORD12 CD133
Has allelic variant	http://purl.bioontology.org/ontology/OMIM/604365.0001 http://purl.bioontology.org/ontology/OMIM/604365.0005 http://purl.bioontology.org/ontology/OMIM/604365.0002 http://purl.bioontology.org/ontology/OMIM/604365.0003 http://purl.bioontology.org/ontology/OMIM/604365.0004
MIMTYPEMEANING	Gene with known sequence
notation	604365
OMIM Entry Type	1
OMIM MimType Value	star
prefLabel	PROMININ 1
tui	T028 T019 T047

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/C567422	Medical Subject Headings	CUI
http://purl.obolibrary.org/obo/PR_000001786	Phenotypic Quality Ontology	LOOM
http://purl.obolibrary.org/obo/PR_000001786	Cell Ontology	LOOM
http://purl.obolibrary.org/obo/PR_000001786	Protein Ontology	LOOM
http://purl.obolibrary.org/obo/PR_000001786	Cell Line Ontology Subset for Chinese National Infrastructure of Cell Line Resource (NICR)	LOOM
http://purl.obolibrary.org/obo/PR_000001786	Cell Line Ontology (Chinese Translation)	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C64344	National Cancer Institute Thesaurus	LOOM
http://purl.bioontology.org/ontology/MESH/C562746	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/C567206	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/C535521	Medical Subject Headings	CUI