(Q18041952)

English

PEX26

protein-coding gene in the species Homo sapiens

PBD7A
PBD7B
PEX26M1T
Pex26pM1T
peroxisomal biogenesis factor 26

In more languages

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000215193

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

Peroxisomal biogenesis factor 26

1 reference

6 July 2017

UniProt protein ID

Peroxisomal biogenesis factor 26 isoform 1

1 reference

UniProt protein ID

21 March 2016

language of work or name

genetic association

Zellweger spectrum disorder

2 references

9 December 2020

https://search.clinicalgenome.org/kb/gene-validity/bf6af95e-6696-420c-8731-d2e37ca6e692--2020-02-07T17:00:00

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_bf6af95e-6696-420c-8731-d2e37ca6e692-2020-02-07T170000.000Z

peroxisomal biogenesis disorder

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000215193/Orphanet_79189

based on heuristic

inferred from an Open Targets association score over 0.7

Zellweger syndrome

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000215193/Orphanet_912

based on heuristic

inferred from an Open Targets association score over 0.7

human chromosome 22

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

18560689

human chromosome 22

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

18077923

human chromosome 22

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

18613905

human chromosome 22

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

18105396

human chromosome 22

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

cytogenetic location

22q11.21

1 reference

15 May 2022

9922

1 reference

15 May 2022

1 reference

HomoloGene build68

9922

1 reference

HomoloGene build68

9922

1 reference

HomoloGene build68

9922

islet of Langerhans

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

prefrontal cortex

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

ganglionic eminence

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

stromal cell of endometrium

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

internal globus pallidus

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

cerebellar vermis

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

left adrenal gland

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000215193

http://identifiers.org/ncbigene/55670

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

1 reference

10 April 2022

Ensembl gene ID

ENSG00000215193

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

Ensembl transcript ID

ENST00000329627

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

ENST00000399744

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

ENST00000428061

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000215193

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(3 entries)

enwiki PEX26
ttwiki PEX26
ukwiki PEX26

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=Q18041952&oldid=1971199291"