Gene
slc16a1a
- ID
- ZDB-GENE-110408-16
- Name
- solute carrier family 16 member 1a
- Symbol
- slc16a1a Nomenclature History
- Previous Names
-
- si:ch211-105j21.7
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to enable lactate:proton symporter activity. Predicted to be involved in plasma membrane lactate transport. Predicted to act upstream of or within monocarboxylic acid transport and transmembrane transport. Predicted to be located in apical plasma membrane. Predicted to be active in basolateral plasma membrane. Human ortholog(s) of this gene implicated in familial hyperinsulinemic hypoglycemia 7. Orthologous to human SLC16A1 (solute carrier family 16 member 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- 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 |
---|---|---|---|
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 | Proton-linked Monocarboxylate Transporter |
---|---|---|---|---|---|---|
UniProtKB:H1ABV8
|
461 | |||||
UniProtKB:E7F7B3
|
461 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
slc16a1a-201
(1)
|
Ensembl | 2,429 nt | ||
mRNA |
slc16a1a-202
(1)
|
Ensembl | 2,439 nt | ||
mRNA |
slc16a1a-203
(1)
|
Ensembl | 1,386 nt |
Interactions and Pathways
No data available
Plasmids
No data available