PVALB (Q18030965)

From Wikidata

Jump to navigation Jump to search

protein-coding gene in the species Homo sapiens

D22S749
parvalbumin

Language	Label	Description	Also known as
English	PVALB	protein-coding gene in the species Homo sapiens	D22S749 parvalbumin

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

protein-coding gene

1 reference

NCBI homo sapiens annotation release 107

3 October 2016

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

1 reference

16 March 2017

UniProt protein ID

Parvalbumin, isoform CRA_a

1 reference

UniProt protein ID

21 March 2016

language of work or name

genetic association

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9970&ncbiId=5816

http://www.genome.gov/gwastudies/index.cfm?gene=PVALB

Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population

25 May 2020

sexual dysfunction

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1876&ncbiId=5816

http://www.genome.gov/gwastudies/index.cfm?gene=PVALB

A genome-wide association study of female sexual dysfunction

25 May 2020

human chromosome 22

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

36800684

human chromosome 22

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

37196728

human chromosome 22

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

36819479

human chromosome 22

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

37215523

human chromosome 22

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

cytogenetic location

22q12.3

1 reference

15 May 2022

2137

1 reference

15 May 2022

2 references

HomoloGene build68

2137

Orthologous MAtrix

https://omabrowser.org/oma/vps/P20472/

1 reference

HomoloGene build68

2137

1 reference

HomoloGene build68

2137

right hemisphere of cerebellum

1

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

primary visual cortex

2

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

superior frontal gyrus

3

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

dorsolateral prefrontal cortex

4

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

right frontal lobe

5

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

muscle of thigh

6

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

7

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

substantia nigra

8

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

Brodmann area 9

9

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

10

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000100362

http://identifiers.org/ncbigene/5816

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

Identifiers

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

Ensembl gene ID

ENSG00000274665

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENSG00000100362

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

Ensembl transcript ID

ENST00000467935

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000630974

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000216200

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000417718

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000625893

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000628536

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000406910

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000443735

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000620986

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000404171

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000627445

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

ENST00000628345

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000100362

Google Knowledge Graph ID

0 references

HGNC gene symbol

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(1 entry)

ukwiki Парвальбумін

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q18030965&oldid=2173686626"