TNFSF15 (Q18034921)

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protein-coding gene in the species Homo sapiens

TL1
TL1A
VEGI
VEGI192A
Vascular endothelial growth inhibitor
TNLG1B
tumor necrosis factor superfamily member 15
TNF superfamily member 15

Language	Label	Description	Also known as
English	TNFSF15	protein-coding gene in the species Homo sapiens	TL1 TL1A VEGI VEGI192A Vascular endothelial growth inhibitor TNLG1B tumor necrosis factor superfamily member 15 TNF superfamily member 15

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000181634

Protein TNFSF15 PDB 2O0O.png
1,200 × 1,000; 385 KB

0 references

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

TNF superfamily member 15

1 reference

6 July 2017

UniProt protein ID

genetic association

primary biliary cholangitis

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12236&ncbiId=9966

http://www.genome.gov/gwastudies/index.cfm?gene=TNFSF15

Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1024&ncbiId=9966

http://www.genome.gov/gwastudies/index.cfm?gene=TNFSF15

Genomewide association study of leprosy

25 May 2020

inflammatory bowel diseases

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0050589&ncbiId=9966

http://www.genome.gov/gwastudies/index.cfm?gene=TNFSF15

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

25 May 2020

Crohn's disease

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_8778&ncbiId=9966

http://www.genome.gov/gwastudies/index.cfm?gene=TNFSF15

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

25 May 2020

human chromosome 9

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

117546915

human chromosome 9

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

114784652

human chromosome 9

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

117568406

human chromosome 9

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

114806039

human chromosome 9

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

cytogenetic location

9q32

1 reference

15 May 2022

3755

1 reference

15 May 2022

Gene Atlas image

PBB GE TNFSF15 221085 at fs.png
732 × 530; 12 KB

0 references

1 reference

HomoloGene build68

3755

1 reference

HomoloGene build68

3755

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

germinal epithelium

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

visceral pleura

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

palpebral conjunctiva

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

pancreatic ductal cell

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

parietal pleura

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000181634

http://identifiers.org/ncbigene/9966

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

ENSG00000181634

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

Ensembl transcript ID

ENST00000374045

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

ENST00000374044

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000181634

0 references

HGNC gene symbol

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

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(4 entries)

cywiki TNFSF15
enwiki Vascular endothelial growth inhibitor
ttwiki TNFSF15
ukwiki TNFSF15

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)

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