HERC2 (Gene)

Synonyms:D15F37S1, ENTREZ:8924, HECT and RLD domain containing E3 ubiquitin protein ligase 2, HERC2, HGNC:4868, MIM:605837, MRT38, NM_004667, NP_004658, SHEP1, XM_005268276, XM_006720726, XM_006720727, XM_017022695, XM_017022696, XM_017022697, XM_017022698, XP_005268333, XP_006720789, XP_006720790, XP_016878184, XP_016878185, XP_016878186, XP_016878187, XR_001751410, XR_931930, jdf2, p528
Id:ENSG00000276802
Description:HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]
This gene belongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All members have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 and a C-terminal HECT (homologous to E6-AP C terminus) domain found in a number of E3 ubiquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variability. Multiple pseudogenes of this gene are located on chromosomes 15 and 16. [provided by RefSeq, Mar 2012]

Analyze

Data Distillery
CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View HERC2'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 HERC2.

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 HERC2.

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 HERC2.

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 HERC2.

Results found

Linked to

 

Label

Description

 

Phenotype

A Phenotype

Phenotype

Autism is a neurodevelopmental disorder characterized by impaired social interaction and communicati...

Phenotype

An elevated lipid concentration in the blood.

Phenotype

Functional anomaly of the kidney persisting for at least three months.

Phenotype

An intermittent cessation of airflow at the mouth and nose during sleep is known as sleep apnea. Apn...

Phenotype

Osteoporosis is a systemic skeletal disease characterized by low bone density and microarchitectural...

Phenotype

Caries is a multifactorial bacterial infection affecting the structure of the tooth. This term has b...

Phenotype

Accumulation of substantial excess body fat.

Phenotype

Smaller than normal size according to sex and gestational age related norms, defined as a weight bel...


  • Phenotype

    Autism is a neurodevelopmental disorder characterized by impaired social interaction and communicati...


  • Phenotype

    An elevated lipid concentration in the blood.


  • Phenotype

    Functional anomaly of the kidney persisting for at least three months.


  • Phenotype

    An intermittent cessation of airflow at the mouth and nose during sleep is known as sleep apnea. Apn...


  • Phenotype

    Osteoporosis is a systemic skeletal disease characterized by low bone density and microarchitectural...


  • Phenotype

    Caries is a multifactorial bacterial infection affecting the structure of the tooth. This term has b...


  • Phenotype

    Accumulation of substantial excess body fat.


  • Phenotype

    Smaller than normal size according to sex and gestational age related norms, defined as a weight bel...

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