CTLA4 (Gene)

Organism:

Homo sapiens

Synonyms:ALPS5, CD, CD152, CELIAC3, CTLA-4, CTLA4, ENTREZ:1493, GRD4, GSE, HGNC:2505, IDDM12, MIM:123890, NM_001037631, NM_005214, NP_001032720, NP_005205, cytotoxic T-lymphocyte associated protein 4

Id:ENSG00000163599

Entrez:1493

Ensembl:ENSG00000163599

Description:cytotoxic T-lymphocyte associated protein 4

Analyze

CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View CTLA4's neighborhood in the knowledge graph.

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Playbook Workflow Builder: Gene-Centric Workflow

View Gene-Centric information about the gene from a pre-built PWB workflow. View the workflow with CTLA4.

CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using CTLA4.

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GDLPA Landing Pages Links

The Gene and Drug Landing Page Aggregator (GDLPA) finds links to primary and secondary source information from CFDE and other resources. Discover landing pages for CTLA4.

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Playbook Workflow Builder

The Playbook Workflow Builder helps you interactively construct workflows leveraging CFDE APIs without code. Start a new workflow with CTLA4.

Results found

Linked to

	Label	Description
	Sensorineural hearing impairment Phenotype (Entity type)	A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlea...
	GSE74251 decitabine MCF-7 0 v 3 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE222758 clofazimine U2OS 0 v 3 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE182150 KIT LSD1 MYC inhibition 6 v 7 human up Gene Set (Entity type)	A Gene Set from LINCS
	GSE114492 GSE153671 KMT2D inhibition 10 v 1 human dn Gene Set (Entity type)	A Gene Set from LINCS
	GSE98856 adenosine 3 v 5 human dn Gene Set (Entity type)	A Gene Set from LINCS
	GSE60217 adenosine 1 v 2 human dn Gene Set (Entity type)	A Gene Set from LINCS
	GSE182680 GSE182683 dexamethasone 7 v 9 human dn Gene Set (Entity type)	A Gene Set from LINCS
	GSE226525 GSE226527 HNRNPH2 knockout 6 v 5 human dn Gene Set (Entity type)	A Gene Set from LINCS
	GSE98856 adenosine 3 v 1 human dn Gene Set (Entity type)	A Gene Set from LINCS

Sensorineural hearing impairment

Phenotype (Entity type)

A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlea...

GSE74251 decitabine MCF-7 0 v 3 human up

Gene Set (Entity type)

A Gene Set from LINCS

GSE222758 clofazimine U2OS 0 v 3 human up

Gene Set (Entity type)

A Gene Set from LINCS

GSE182150 KIT LSD1 MYC inhibition 6 v 7 human up

Gene Set (Entity type)

A Gene Set from LINCS

GSE114492 GSE153671 KMT2D inhibition 10 v 1 human dn

Gene Set (Entity type)

A Gene Set from LINCS

GSE98856 adenosine 3 v 5 human dn

Gene Set (Entity type)

A Gene Set from LINCS

GSE60217 adenosine 1 v 2 human dn

Gene Set (Entity type)

A Gene Set from LINCS

GSE182680 GSE182683 dexamethasone 7 v 9 human dn

Gene Set (Entity type)

A Gene Set from LINCS

GSE226525 GSE226527 HNRNPH2 knockout 6 v 5 human dn

Gene Set (Entity type)

A Gene Set from LINCS

GSE98856 adenosine 3 v 1 human dn

Gene Set (Entity type)

A Gene Set from LINCS

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@CFDE Workbench 2026

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

Consortium

Community

Resources

CFDE Workbench

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

@CFDE Workbench 2026

This repository is under review for potential modification in compliance with Administration directives.