Gene
tmem165
- ID
- ZDB-GENE-030131-3222
- Name
- transmembrane protein 165
- Symbol
- tmem165 Nomenclature History
- Previous Names
-
- si:ch211-278f21.2
- tparl (1)
- wu:fc31a09
- zgc:92342
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Predicted to have calcium ion transmembrane transporter activity and manganese ion transmembrane transporter activity. Involved in osteoblast differentiation; protein N-linked glycosylation; and skeletal system development. Predicted to localize to Golgi apparatus. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIk. Is expressed in head; heart; and heart tube. Orthologous to human TMEM165 (transmembrane protein 165).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Bammens et al., 2015
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 6 figures from Bammens et al., 2015
- 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 IIk | Alliance | Congenital disorder of glycosylation, type IIk | 614727 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | GDT1-like | GDT1-like, conserved site |
|---|---|---|---|
|
UniProtKB:Q8JJ62
|
305 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
tmem165-201
(1)
|
Ensembl | 2,163 nt |
Interactions and Pathways
No data available
Plasmids
No data available