RELN

GENERAL INFORMATION

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Gene name

RELN

Gene description

Reelin

Protein class

Disease related genes
Plasma proteins
Predicted intracellular proteins
Predicted secreted proteins

Predicted localization

Intracellular,Secreted

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (liver)
GTEx:Group enriched (cerebellum)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (liver)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (cerebellum)

Organ

Expression



GENE INFORMATION

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Gene name

RELN (HGNC Symbol)

Synonyms

PRO1598, RL

Description

Reelin (HGNC Symbol)

Entrez gene summary

This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008]

Chromosome

7

Cytoband

q22.1

Chromosome location (bp)

103471784 - 103989516

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000189056 (version 78.38)

Entrez gene

5649

UniProt

P78509 (UniProt - Evidence at protein level)

neXtProt

NX_P78509

Antibodypedia

RELN antibodies


PROTEIN BROWSER

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ENST00000343529
 
ENST00000424685
 
ENST00000428762
 
ENST00000429186
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

RELN-001 ENSP00000392423
ENST00000428762
P78509
Show all »
Show » Show » 3460 388.4 Yes 0
RELN-002 ENSP00000345694
ENST00000343529
P78509
Show all »
Show » Show » 3458 388.2 Yes 0
RELN-009 ENSP00000404818
ENST00000429186
Show » 68 7.9 No 0
RELN-201 ENSP00000388446
ENST00000424685
J3KQ66
Show all »
Show » Show » 3460 388.4 Yes 0