Open main menu
Home
Random
Nearby
Log in
Settings
About Wikidata
Disclaimers
Wikidata
Search
(Q414043)
Watch
English
RELN
protein-coding gene in the species Homo sapiens
LIS2
PRO1598
RL
reelin
ETL7
In more languages
edit
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
Commons category
Reelin
1 reference
imported from Wikimedia project
English Wikipedia
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
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
Sitelinks
Wikipedia
(1 entry)
edit
ukwiki
Рілін
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Other sites
(0 entries)
edit
