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(Q414043)
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English
RELN
protein-coding gene in the species Homo sapiens
LIS2
PRO1598
RL
reelin
ETL7
In more languages
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Statements
instance of
gene
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
subclass of
protein-coding gene
1 reference
stated in
Ensembl Release 87
Ensembl gene ID
ENSG00000189056
image
2DDU.png
1,440 × 1,080; 530 KB
0 references
found in taxon
Homo sapiens
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
encodes
Reelin
1 reference
stated in
UniProt
retrieved
6 July 2017
UniProt protein ID
P78509
genetic association
Alzheimer's disease
determination method
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10652&ncbiId=5649
http://www.genome.gov/gwastudies/index.cfm?gene=RELN
stated in
Phenocarta
Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study
retrieved
25 May 2020
otosclerosis
determination method
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12185&ncbiId=5649
http://www.genome.gov/gwastudies/index.cfm?gene=RELN
stated in
Phenocarta
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis
retrieved
25 May 2020
multiple sclerosis
determination method
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_2377&ncbiId=5649
http://www.genome.gov/gwastudies/index.cfm?gene=RELN
stated in
Phenocarta
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
retrieved
25 May 2020
schizophrenia
determination method
genome-wide association study
TAS
1 reference
reference URL
https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_5419&ncbiId=5649
http://www.genome.gov/gwastudies/index.cfm?gene=RELN
stated in
Phenocarta
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women
retrieved
25 May 2020
Norman–Roberts syndrome
1 reference
stated in
UniProt
UniProt protein ID
P78509
retrieved
13 August 2019
familial temporal lobe epilepsy 7
1 reference
stated in
UniProt
UniProt protein ID
P78509
retrieved
13 August 2019
chromosome
human chromosome 7
genomic assembly
Genome assembly GRCh38
Genome assembly GRCh37
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
strand orientation
reverse strand
genomic assembly
Genome assembly GRCh38
Genome assembly GRCh37
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
genomic start
103471784
chromosome
human chromosome 7
genomic assembly
Genome assembly GRCh38
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
103112231
chromosome
human chromosome 7
genomic assembly
Genome assembly GRCh37
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
genomic end
103629963
chromosome
human chromosome 7
genomic assembly
Genome assembly GRCh37
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
103989658
chromosome
human chromosome 7
genomic assembly
Genome assembly GRCh38
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
cytogenetic location
7q22.1
1 reference
stated in
NCBI Gene
retrieved
8 February 2020
Entrez Gene ID
5649
Gene Atlas Image
PBB GE RELN 205923 at fs.png
732 × 530; 11 KB
0 references
ortholog
Reln
found in taxon
brown rat
1 reference
stated in
HomoloGene build68
HomoloGene ID
3699
Reln
found in taxon
house mouse
1 reference
stated in
HomoloGene build68
HomoloGene ID
3699
reln
found in taxon
Danio rerio
1 reference
stated in
HomoloGene build68
HomoloGene ID
3699
HomoloGene ID
3699
1 reference
stated in
NCBI Gene
retrieved
8 February 2020
Entrez Gene ID
5649
exact match
http://identifiers.org/ncbigene/5649
1 reference
stated in
Identifiers.org Registry
reference URL
http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
Commons category
Reelin
1 reference
imported from Wikimedia project
English Wikipedia
Identifiers
RefSeq RNA ID
NM_173054
1 reference
stated in
NCBI Gene
retrieved
8 February 2020
Entrez Gene ID
5649
NM_005045
1 reference
stated in
NCBI Gene
retrieved
8 February 2020
Entrez Gene ID
5649
Ensembl gene ID
ENSG00000189056
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
Ensembl transcript ID
ENST00000478148
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
ENST00000343529
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
ENST00000424685
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
ENST00000428762
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
ENST00000429186
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
ENST00000473457
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
ENST00000473945
1 reference
stated in
Ensembl Release 99
Ensembl gene ID
ENSG00000189056
Entrez Gene ID
5649
1 reference
stated in
NCBI Gene
retrieved
8 February 2020
Entrez Gene ID
5649
HGNC gene symbol
RELN
1 reference
stated in
NCBI Gene
retrieved
8 February 2020
Entrez Gene ID
5649
HGNC ID
9957
1 reference
stated in
NCBI Gene
retrieved
8 February 2020
Entrez Gene ID
5649
OMIM ID
600514
1 reference
stated in
Online Mendelian Inheritance in Man
retrieved
19 August 2019
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Wiktionary
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Multilingual sites
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