Gene

slc6a19a.2

ID
ZDB-GENE-141210-16
Name
solute carrier family 6 member 19a, tandem duplicate 2
Symbol
slc6a19a.2 Nomenclature History
Previous Names
  • si:ch73-166j22.4 (1)
Type
protein_coding_gene
Location
Chr: 19 Mapping Details/Browsers
Description
Predicted to have symporter activity. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in Hartnup disease. Orthologous to human SLC6A19 (solute carrier family 6 member 19).
Genome Resources
Note
None
Expression
All Expression Data
1 figure from Mathiyalagan et al., 2019
Cross-Species Comparison
High Throughput Data
Thisse Expression 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 slc6a19a.2 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Hartnup disease Alliance Hartnup disorder 234500
iminoglycinuria Alliance Iminoglycinuria, digenic 242600
Hyperglycinuria 138500
Associated With slc6a19a.2 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR000175 Sodium:neurotransmitter symporter
Homologous_superfamily IPR037272 Sodium:neurotransmitter symporter superfamily
Domain Details Per Protein
Protein Length Sodium:neurotransmitter symporter Sodium:neurotransmitter symporter superfamily
UniProtKB:A0A2R8QC26 320
UniProtKB:E7EY30 647
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Gene Tree
Ensembl
Citations