Gene

slc30a10

ID
ZDB-GENE-060608-2
Name
solute carrier family 30 member 10
Symbol
slc30a10 Nomenclature History
Previous Names
  • ZnT10 (1)
Type
protein_coding_gene
Location
Chr: 13 Mapping Details/Browsers
Description
Predicted to have cation transmembrane transporter activity. Involved in manganese ion homeostasis and manganese ion transport. Predicted to localize to plasma membrane. Human ortholog(s) of this gene implicated in hypermanganesemia with dystonia 1. Is expressed in brain; liver; and yolk syncytial layer. Orthologous to human SLC30A10 (solute carrier family 30 member 10).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Xia et al., 2017
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
5 figures from Xia et al., 2017
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc30a10 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
hypermanganesemia with dystonia 1 Alliance Hypermanganesemia with dystonia 1 613280
Associated With slc30a10 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR002524 Cation efflux protein
Homologous_superfamily IPR027469 Cation efflux transmembrane domain superfamily
Domain Details Per Protein
Protein Length Cation efflux protein Cation efflux transmembrane domain superfamily
UniProtKB:A8WFU0 385
UniProtKB:A0A0R4IEQ2 385
Transcripts
Genome Browsers
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA slc30a10-201 (1) Ensembl 2,067 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations