SLC39A4 (Gene)

Synonyms:AEZ, AWMS2, ENTREZ:55630, HGNC:17129, MIM:607059, NM_001280557, NM_001374839, NM_017767, NM_130849, NP_001267486, NP_001361768, NP_060237, NP_570901, SLC39A4, XM_024447189, XP_024302957, ZIP4, solute carrier family 39 member 4
Id:ENSG00000285243
Description:solute carrier family 39 member 4 [Source:HGNC Symbol;Acc:HGNC:17129]
This gene encodes a member of the zinc/iron-regulated transporter-like protein (ZIP) family. The encoded protein localizes to cell membranes and is required for zinc uptake in the intestine. Mutations in this gene result in acrodermatitis enteropathica. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]

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Data Distillery
CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View SLC39A4'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 SLC39A4.

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 SLC39A4.

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 SLC39A4.

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 SLC39A4.

Results found

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Label

Description

 

Phenotype

A noncongenital process of hair loss, which may progress to partial or complete baldness.

  • Phenotype

    A noncongenital process of hair loss, which may progress to partial or complete baldness.

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