GRHL2 (Gene)

Synonyms:BOM, DFNA28, ECTDS, ENTREZ:79977, GRHL2, HGNC:2799, MIM:608576, NM_001330593, NM_024915, NP_001317522, NP_079191, PPCD4, TFCP2L3, XM_011517306, XM_011517307, XM_024447286, XP_011515608, XP_011515609, XP_024303054, grainyhead like transcription factor 2
Omim:OMIM:608576
Id:ENSG00000083307
Hgnc:HGNC:2799
Entrez:79977
Description:grainyhead like transcription factor 2
The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]

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Data Distillery
CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View GRHL2's neighborhood in the knowledge graph.

Playbook Workflow Builder
Playbook Workflow Builder: Gene-Centric Workflow

View Gene-Centric information about the gene from a pre-built PWB workflow. View the workflow with GRHL2.

Gene Partnership Appyter
CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using GRHL2.

Gene and Drug Landing Page Aggregator
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 GRHL2.

Playbook Workflow Builder
Playbook Workflow Builder

The Playbook Workflow Builder helps you interactively construct workflows leveraging CFDE APIs without code. Start a new workflow with GRHL2.

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