Gene
slc6a19b
- ID
- ZDB-GENE-030131-4755
- Name
- solute carrier family 6 member 19b
- Symbol
- slc6a19b Nomenclature History
- Previous Names
-
- slc6a19
- wu:fd58f10
- zgc:66050 (1)
- Type
- protein_coding_gene
- Location
- Chr: 16 Mapping Details/Browsers
- Description
- Predicted to have neurotransmitter:sodium symporter activity. Predicted to localize to plasma membrane. Human ortholog(s) of this gene implicated in Hartnup disease. Is expressed in floor plate; pronephric duct; and yolk syncytial layer. Orthologous to human SLC6A19 (solute carrier family 6 member 19).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 8 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:66050 (8 images)
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 | Sodium:neurotransmitter symporter | Sodium:neurotransmitter symporter superfamily |
|---|---|---|---|
|
UniProtKB:Q6PBA3
|
651 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc6a19b-201
(1)
|
Ensembl | 2,538 nt |
Interactions and Pathways
No data available
Plasmids
No data available