Gene
slc16a1b
- ID
- ZDB-GENE-030515-5
- Name
- solute carrier family 16 member 1b
- Symbol
- slc16a1b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 8 Mapping Details/Browsers
- Description
- Predicted to have monocarboxylic acid transmembrane transporter activity. Predicted to be involved in monocarboxylic acid transport. Predicted to localize to integral component of plasma membrane. Human ortholog(s) of this gene implicated in familial hyperinsulinemic hypoglycemia 7. Is expressed in several structures, including central nervous system; digestive system; liver primordium; musculature system; and neural tube. Orthologous to human SLC16A1 (solute carrier family 16 member 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 13 figures from 4 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cb517 (22 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 |
|---|---|---|---|
| familial hyperinsulinemic hypoglycemia 7 | Alliance | Hyperinsulinemic hypoglycemia, familial, 7 | 610021 |
| Erythrocyte lactate transporter defect | 245340 | ||
| Monocarboxylate transporter 1 deficiency | 616095 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Major facilitator superfamily | Major facilitator superfamily domain | MFS transporter superfamily | Monocarboxylate transporter |
|---|---|---|---|---|---|
|
UniProtKB:Q7ZUL1
|
461 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
slc16a1b-201
(1)
|
Havana | 2205 nt |
Interactions and Pathways
No data available
Plasmids
No data available