Gene

slc7a7

ID
ZDB-GENE-051127-5
Name
solute carrier family 7 member 7
Symbol
slc7a7 Nomenclature History
Previous Names
  • unm t30713
  • unm_t30713
  • zgc:123300
Type
protein_coding_gene
Location
Chr: 7 Mapping Details/Browsers
Description
Predicted to have L-amino acid transmembrane transporter activity and basic amino acid transmembrane transporter activity. Involved in microglia development. Predicted to localize to integral component of membrane. Is expressed in brain; myeloid cell; and pancreatic D cell. Used to study lysinuric protein intolerance. Human ortholog(s) of this gene implicated in lysinuric protein intolerance. Orthologous to human SLC7A7 (solute carrier family 7 member 7).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
4 figures from 4 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
3 figures from 2 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc7a7 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
lysinuric protein intolerance Alliance Lysinuric protein intolerance 222700
Associated With slc7a7 Via Experimental Models
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR002293 Amino acid/polyamine transporter I
Domain Details Per Protein
Protein Length Amino acid/polyamine transporter I
UniProtKB:Q2YDQ4 501
UniProtKB:F1R8V8 501
Transcripts
Genome Browsers
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