CTLA4 (Q14875744)

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protein-coding gene in the species Homo sapiens

ALPS5
CD
CD152
CELIAC3
CTLA-4
GRD4
GSE
IDDM12
cytotoxic T-lymphocyte associated protein 4

Language	Label	Description	Also known as
English	CTLA4	protein-coding gene in the species Homo sapiens	ALPS5 CD CD152 CELIAC3 CTLA-4 GRD4 GSE IDDM12 cytotoxic T-lymphocyte associated protein 4

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000163599

CTLA4 Crystal Structure.rsh.png
739 × 750; 244 KB

Structure cristalline de CTLA4 telle que publiée dans la Protein Data Bank (PDB : 1DQT) (French)

0 references

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

cytotoxic T-lymphocyte associated protein 4

1 reference

6 July 2017

UniProt protein ID

genetic association

rheumatoid arthritis

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_7148&ncbiId=1493

http://www.genome.gov/gwastudies/index.cfm?gene=CTLA4

Genetics of rheumatoid arthritis contributes to biology and drug discovery

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1459&ncbiId=1493

http://www.genome.gov/gwastudies/index.cfm?gene=CTLA4

Novel associations for hypothyroidism include known autoimmune risk loci

25 May 2020

type-1 diabetes

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9744&ncbiId=1493

http://www.genome.gov/gwastudies/index.cfm?gene=CTLA4

Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.

25 May 2020

type 1 diabetes mellitus 12

1 reference

UniProt protein ID

13 August 2019

autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency

4 references

26 January 2021

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_e79675bd-3eef-4925-b4ef-3b7c48734f30-2021-01-26T171103.720Z

18 March 2021

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_e79675bd-3eef-4925-b4ef-3b7c48734f30-2021-03-16T133941.848Z

19 May 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_e79675bd-3eef-4925-b4ef-3b7c48734f30-2021-04-28T163716.269Z

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000163599/MONDO_0014493

based on heuristic

inferred from an Open Targets association score over 0.7

human chromosome 2

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

204732509

human chromosome 2

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

203853888

human chromosome 2

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

204738683

human chromosome 2

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

203873965

human chromosome 2

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

cytogenetic location

2q33.2

1 reference

15 May 2022

3820

1 reference

15 May 2022

Gene Atlas image

PBB GE CTLA4 221331 x at fs.png
732 × 530; 11 KB

0 references

1 reference

HomoloGene build68

3820

1 reference

HomoloGene build68

3820

1

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

2

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

pancreatic epithelial cell

3

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

pancreatic ductal cell

4

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

superficial temporal artery

5

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

6

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

7

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

8

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

9

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

10

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000163599

http://identifiers.org/ncbigene/1493

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

0 references

Ensembl gene ID

ENSG00000163599

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

Ensembl transcript ID

ENST00000487393

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

ENST00000295854

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

ENST00000427473

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

ENST00000650075

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

ENST00000648405

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

ENST00000696479

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

ENST00000696049

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000163599

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(0 entries)

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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