Gene

slc39a13

ID
ZDB-GENE-030616-17
Name
solute carrier family 39 member 13
Symbol
slc39a13 Nomenclature History
Previous Names
  • ZIP13 (1)
  • si:by184l24.1
  • si:xx-184l24.1
  • wu:fa55a07
  • zgc:136440
Type
protein_coding_gene
Location
Chr: 7 Mapping Details/Browsers
Description
Predicted to have zinc ion transmembrane transporter activity. Predicted to be involved in cellular zinc ion homeostasis and zinc ion transmembrane transport. Predicted to localize to Golgi membrane and integral component of membrane. Human ortholog(s) of this gene implicated in Ehlers-Danlos syndrome. Orthologous to human SLC39A13 (solute carrier family 39 member 13).
Genome Resources
Note
None
Expression
All Expression Data
2 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc39a13 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Ehlers-Danlos syndrome spondylodysplastic type 3 Alliance Ehlers-Danlos syndrome, spondylodysplastic type, 3 612350
Associated With slc39a13 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR003689 Zinc/iron permease
Domain Details Per Protein
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Ensembl Gene Tree
Citations