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
Expression
All Expression Data
1 figure from Thisse et al., 2004
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With tmem199 Human Ortholog
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
Associated With tmem199 Via Experimental Models
No data available
Gene Ontology
Protein Domains
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
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations