Gene

slc38a8b

ID
ZDB-GENE-121005-6
Name
solute carrier family 38 member 8b
Symbol
slc38a8b Nomenclature History
Previous Names
None
Type
protein_coding_gene
Location
Chr: 7 Mapping Details/Browsers
Description
Predicted to localize to integral component of membrane. Orthologous to human SLC38A8 (solute carrier family 38 member 8).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
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 slc38a8b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
foveal hypoplasia 2 Alliance Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis 609218
Associated With slc38a8b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR013057 Amino acid transporter, transmembrane domain
Domain Details Per Protein
Protein Length Amino acid transporter, transmembrane domain
UniProtKB:A0A8M9PPQ5 444
Transcripts
Genome Browsers
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA slc38a8b-201 (1) Ensembl 1,876 nt
mRNA slc38a8b-202 (1) Ensembl 1,932 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