OSCAR (Gene)

Organism:

Homo sapiens

Synonyms:ENTREZ:126014, HGNC:29960, MIM:606862, NM_001282349, NM_001282350, NM_130771, NM_133168, NM_133169, NM_206817, NM_206818, NP_001269278, NP_001269279, NP_570127, NP_573398, NP_573399, NP_996554, OSCAR, PIGR3, PIgR-3, osteoclast associated Ig-like receptor

Id:ENSG00000278533

Description:osteoclast associated Ig-like receptor [Source:HGNC Symbol;Acc:HGNC:29960]

Osteoclasts are multinucleated cells that resorb bone and are essential for bone homeostasis. This gene encodes an osteoclast-associated receptor (OSCAR), which is a member of the leukocyte receptor complex protein family that plays critical roles in the regulation of both innate and adaptive immune responses. The encoded protein may play a role in oxidative stress-mediated atherogenesis as well as monocyte adhesion. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]

Analyze

CFDE DD-Knowledge Graph

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

Submit

Playbook Workflow Builder: Gene-Centric Workflow

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

CFDE Gene-Centric Appyter

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

Submit

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 OSCAR.

Submit

Playbook Workflow Builder

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

Results found

Linked to

	Label	Description
	Hepatic failure Phenotype (Entity type)	A Phenotype
	Abnormality of mitochondrial metabolism Phenotype (Entity type)	A functional anomaly of mitochondria.

Hepatic failure

Phenotype (Entity type)

A Phenotype

Abnormality of mitochondrial metabolism

Phenotype (Entity type)

A functional anomaly of mitochondria.

DISPLAY PER PAGE

CFDE Workbench

Consortium

Community

Resources

@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.