Online Mendelian Inheritance in Man

Last uploaded: August 28, 2024

Preferred Name	AGRIN
Synonyms	MYASTHENIC SYNDROME, CONGENITAL, 8 AGRN
ID	http://purl.bioontology.org/ontology/OMIM/103320
altLabel	MYASTHENIC SYNDROME, CONGENITAL, 8 AGRN
cui	C3808739 C1412285
Gene Locus	1pter-p32
Gene Symbol	CMS8 AGRN
Has allelic variant	http://purl.bioontology.org/ontology/OMIM/103320.0001 http://purl.bioontology.org/ontology/OMIM/103320.0003 http://purl.bioontology.org/ontology/OMIM/103320.0002
MIMTYPEMEANING	Gene with known sequence
notation	103320
OMIM Entry Type	1
OMIM MimType Value	star
prefLabel	AGRIN
tui	T047 T028

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/PR_000003845	OBA	LOOM
http://www.semanticweb.org/admin/ontologies/2022/7/MIO:01444	MIO	LOOM
http://purl.obolibrary.org/obo/IMR_0001134	HOIP	LOOM
http://purl.obolibrary.org/obo/IMR_0001134	TXPO	LOOM
http://www.orpha.net/ORDO/Orphanet_233062	ORDO	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D12.776.641.050	RH-MESH	LOOM
http://purl.org/obo/owlapi/fma#FMA_82835	BIOMODELS	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D018171	RH-MESH	LOOM
http://purl.org/sig/ont/fma/fma82835	FMA	LOOM
http://purl.bioontology.org/ontology/MESH/D018171	MESH	LOOM
http://purl.bioontology.org/ontology/CSP/4006-0001	CRISP	LOOM
http://purl.obolibrary.org/obo/PR_000003845	PR	LOOM
http://purl.obolibrary.org/obo/PR_000003845	CCONT	LOOM
http://purl.obolibrary.org/obo/PR_000003845	EFO	LOOM
http://purl.obolibrary.org/obo/PR_000003845	NIFSTD	LOOM
http://purl.obolibrary.org/obo/OMIT_0018404	OMIT	LOOM
http://www.ncbi.nlm.nih.gov/gene/11603	NIFSTD	LOOM
http://id.nlm.nih.gov/mesh/D018171	MDM	LOOM
http://purl.jp/bio/4/id/200906041558561283	IOBC	LOOM
http://www.phoc.org.cn/pmo/class/PMO_00023622	PMAPP-PMO	LOOM
http://purl.obolibrary.org/obo/MESH_D018171	BERO	LOOM
http://www.limics.org/hrdo/rdfns#gen_id_19233	HRDO	LOOM