(Q14883734)

English

WRN

protein-coding gene in the species Homo sapiens

RECQ3
RECQL2
RECQL3
Werner syndrome RecQ like helicase
WRN RecQ like helicase

In more languages

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Statements

1 reference

1 reference

Protein WRN PDB 2axl.png
595 × 303; 60 KB

0 references

1 reference

Werner syndrome RecQ like helicase

1 reference

6 July 2017

5 references

https://ghr.nlm.nih.gov/condition/werner-syndrome#genes

retrieved

13 December 2018

quotation

Mutations in the WRN gene cause Werner syndrome. (English)

13 August 2019

9 December 2020

https://search.clinicalgenome.org/kb/gene-validity/d9c04f29-bc94-40c5-95d7-d25d21cd387f--2018-10-09T17:00:00

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_d9c04f29-bc94-40c5-95d7-d25d21cd387f-2018-10-09T170000.000Z

stated in

Open Targets Platform

retrieved

24 August 2023

reference URL

https://platform.opentargets.org/evidence/ENSG00000165392/MONDO_0010196

based on heuristic

inferred from an Open Targets association score over 0.7

1 reference

13 August 2019

genome assembly GRCh38

Genome assembly GRCh37

1 reference

genome assembly GRCh38

Genome assembly GRCh37

1 reference

30891317

Genome assembly GRCh37

1 reference

31033788

genome assembly GRCh38

1 reference

31031285

Genome assembly GRCh37

1 reference

31176138

genome assembly GRCh38

1 reference

8p12

1 reference

15 May 2022

6659

1 reference

15 May 2022

PBB GE WRN 205667 at fs.png
732 × 530; 11 KB

0 references

1 reference

6659

1 reference

6659

1 reference

6659

Caenorhabditis elegans

1 reference

6659

1

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

sperm

series ordinal

2

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

gastric mucosa

series ordinal

3

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

secondary oocyte

series ordinal

4

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

sural nerve

series ordinal

5

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

skin of abdomen

series ordinal

6

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

body of pancreas

series ordinal

7

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

left uterine tube

series ordinal

8

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

bone marrow

series ordinal

9

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

rectum

series ordinal

10

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000165392

exact match

http://identifiers.org/ncbigene/7486

1 reference

stated in

Identifiers.org

reference URL

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

Commons category

Werner syndrome ATP-dependent helicase, WRN

0 references

Identifiers

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

Ensembl transcript ID

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

0 references

1 reference

15 May 2022

1 reference

15 May 2022

Microsoft Academic ID

0 references

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

inferred by common HGNC mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

15 June 2023

Sitelinks

Wikipedia(10 entries)

bswiki WRN
cywiki WRN
enwiki Werner syndrome helicase
eswiki WRN
glwiki WRN
jawiki WRN
shwiki WRN (gen)
srwiki WRN (gen)
ttwiki WRN
ukwiki WRN

(Q14883734)

WRN

Statements

Identifiers

Sitelinks

Wikipedia(10 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)