Gene
slc6a19a.1
- ID
- ZDB-GENE-070620-2
- Name
- solute carrier family 6 member 19a, tandem duplicate 1
- Symbol
- slc6a19a.1 Nomenclature History
- Previous Names
-
- slc6a19a
- zgc:162095 (1)
- Type
- protein_coding_gene
- Location
- Chr: 19 Mapping Details/Browsers
- Description
- Predicted to enable symporter activity. Predicted to be involved in sodium ion transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. Human ortholog(s) of this gene implicated in Hartnup disease and iminoglycinuria. Orthologous to human SLC6A19 (solute carrier family 6 member 19).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Mathiyalagan et al., 2019
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Hartnup disease | Alliance | Hartnup disorder | 234500 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Neutral amino acid SLC6 transporter | Sodium:neurotransmitter symporter | Sodium:neurotransmitter symporter superfamily |
|---|---|---|---|---|
|
UniProtKB:A5D6R9
|
629 | |||
|
UniProtKB:Q1RLZ0
|
660 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc6a19a.1-201
(1)
|
Ensembl | 3,908 nt |
Interactions and Pathways
No data available
Plasmids
No data available