MLLT6 (Gene)

Synonyms:AF17, ENTREZ:4302, HGNC:7138, MIM:600328, MLLT6, MLLT6, PHD finger containing, NM_005937, NP_005928
Id:ENSG00000275851
Description:MLLT6, PHD finger containing [Source:HGNC Symbol;Acc:HGNC:7138]
Enables histone binding activity and nucleosome binding activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including negative regulation of histone H3-K79 methylation; renal potassium excretion; and renal sodium excretion. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

Analyze

Data Distillery
CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View MLLT6'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 MLLT6.

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 MLLT6.

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 MLLT6.

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 MLLT6.

Results found

Linked to

 

Label

Description

 

Phenotype

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

  • Phenotype

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

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