Orphanet Rare Disease Ontology

Last uploaded: December 13, 2023

Preferred Name	RAD51 recombinase
Synonyms	HsT16930
ID	http://www.orpha.net/ORDO/Orphanet_118208
alternative_term	HsT16930 HsRad51 BRCA1/BRCA2-containing complex, subunit 5 BRCC5 FANCR
hasDbXref	Ensembl:ENSG00000051180 OMIM:179617 SwissProt:Q06609 Reactome:Q06609 Genatlas:RAD51 HGNC:9817
label	RAD51 recombinase
prefixIRI	ORDO:Orphanet_118208
prefLabel	RAD51 recombinase
symbol	RAD51
subClassOf	http://www.orpha.net/ORDO/Orphanet_410298

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D051135	RH-MESH	LOOM
http://purl.obolibrary.org/obo/OMIT_0024686	OMIT	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D12.776.260.695	RH-MESH	LOOM
http://id.nlm.nih.gov/mesh/D051135	MDM	LOOM
http://purl.jp/bio/4/id/200906071906007968	IOBC	LOOM
http://purl.bioontology.org/ontology/OMIM/179617	OMIM	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D08.811.739.650.500	RH-MESH	LOOM
http://purl.obolibrary.org/obo/MESH_D051135	BERO	LOOM
http://purl.bioontology.org/ontology/MESH/D051135	MESH	LOOM
http://www.phoc.org.cn/pmo/class/PMO_00020862	PMAPP-PMO	LOOM