Gene
tmem199
- ID
- ZDB-GENE-050522-150
- Name
- transmembrane protein 199
- Symbol
- tmem199 Nomenclature History
- Previous Names
-
- zgc:109974
- Type
- protein_coding_gene
- Location
- Chr: 15 Mapping Details/Browsers
- Description
- Predicted to be involved in vacuolar proton-transporting V-type ATPase complex assembly. Predicted to localize to endomembrane system. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIp. Orthologous to human TMEM199 (transmembrane protein 199).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:109974 (1 image)
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 |
|---|---|---|---|
| congenital disorder of glycosylation type IIp | Alliance | Congenital disorder of glycosylation, type IIp | 616829 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR021013 | ATPase, vacuolar ER assembly factor, Vma12 |
Domain Details Per Protein
| Protein | Length | ATPase, vacuolar ER assembly factor, Vma12 |
|---|---|---|
|
UniProtKB:A8E5C6
|
195 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
tmem199-201
(1)
|
Ensembl | 435 nt | ||
| mRNA |
tmem199-202
(1)
|
Ensembl | 863 nt |
Interactions and Pathways
No data available
Plasmids
No data available