B3GALNT2 (Gene)

Organism:

Homo sapiens

Synonyms:B3GALNT2, B3GalNAc-T2, ENTREZ:148789, HGNC:28596, MDDGA11, MIM:610194, NM_001277155, NM_152490, NP_001264084, NP_689703, XM_006711749, XM_017000394, XM_017000395, XP_006711812, XP_016855883, XP_016855884, XR_001736987, XR_001736988, XR_001736989, XR_001736990, beta-1, 3-N-acetylgalactosaminyltransferase 2

Id:ENSG00000282880

Description:beta-1,3-N-acetylgalactosaminyltransferase 2 [Source:HGNC Symbol;Acc:HGNC:28596]

This gene encodes a member of the glycosyltransferase 31 family. The encoded protein synthesizes GalNAc:beta-1,3GlcNAc, a novel carbohydrate structure, on N- and O-glycans. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Mar 2013]

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CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View B3GALNT2'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 B3GALNT2.

CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using B3GALNT2.

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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 B3GALNT2.

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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 B3GALNT2.

Results found

Linked to

	Label	Description
	Glaucoma Phenotype (Entity type)	Glaucoma refers loss of retinal ganglion cells in a characteristic pattern of optic neuropathy usual...
	Myopathy Phenotype (Entity type)	A disorder of muscle unrelated to impairment of innervation or neuromuscular junction.
	Muscular dystrophy Phenotype (Entity type)	The term dystrophy means abnormal growth. However, muscular dystrophy is used to describe primary my...

Glaucoma

Phenotype (Entity type)

Glaucoma refers loss of retinal ganglion cells in a characteristic pattern of optic neuropathy usual...

Myopathy

Phenotype (Entity type)

A disorder of muscle unrelated to impairment of innervation or neuromuscular junction.

Muscular dystrophy

Phenotype (Entity type)

The term dystrophy means abnormal growth. However, muscular dystrophy is used to describe primary my...

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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

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