Preferred Name

REELIN

Synonyms

RL

ID

http://purl.bioontology.org/ontology/OMIM/600514

altLabel

RL

LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE

RELN

EPILEPSY, FAMILIAL TEMPORAL LOBE, 7

cui

C0796089

C4225327

C1419337

Gene Locus

7q22

Gene Symbol

RL

LIS2

ETL7

RELN

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/600514.0006

http://purl.bioontology.org/ontology/OMIM/600514.0004

http://purl.bioontology.org/ontology/OMIM/600514.0005

http://purl.bioontology.org/ontology/OMIM/600514.0001

http://purl.bioontology.org/ontology/OMIM/600514.0002

http://purl.bioontology.org/ontology/OMIM/600514.0003

MIMTYPEMEANING

Gene with known sequence

notation

600514

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

REELIN

tui

T028

T047

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://www.orpha.net/ORDO/Orphanet_118272 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bioontology.org/ontology/MESH/C537848 Medical Subject Headings / 医学主题词表 CUI
http://purl.obolibrary.org/obo/PR_000013879 Protein Ontology / 蛋白质本体 LOOM
http://purl.obolibrary.org/obo/PR_000013879 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/PR_000013879 Cell Ontology / 细胞本体 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C102801 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM