reelin

Summary
Gene Symbol
  • RELN
Organism
Homo sapiens (human)
NCBI Gene
5649
PubChem
5649
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Calcium
  • Cell adhesion
  • Developmental protein
  • Disease variant
  • Disulfide bond
  • EGF-like domain
  • Epilepsy
  • Extracellular matrix
  • Glycoprotein
  • Lissencephaly
  • Metal-binding
  • Reference proteome
  • Repeat
  • Serine protease
  • Signal
  • Zinc
Proteins
Displaying 1 entry
UniProt Protein Name
P78509
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
protein
Functional Category
  • E: Amino acid transport and metabolism
  • M: Cell wall/membrane/envelope biogenesis
  • T: Signal transduction mechanisms
Displaying all 2 entries
InterPro
Exostosin, GT47 domain
Exostosin-like
Disease
Disease Ontology
Displaying entries 1 - 10 of 11 in total
DO ID Disease Name Source
DOID:0060751 familial temporal lobe epilepsy 7
DOID:0060902 Norman-Roberts syndrome
DOID:10652 Alzheimer's disease
DOID:12849 autistic disorder
DOID:14250 Down syndrome
DOID:1459 hypothyroidism
DOID:1824 status epilepticus
DOID:3312 bipolar disorder
DOID:3328 temporal lobe epilepsy
DOID:5082 liver cirrhosis

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024