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. Is expressed in head; heart; and heart tube. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIk. Orthologous to human TMEM165 (transmembrane protein 165).
Genome Resources
Note
None
Comparative Information
Expression
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
Phenotype
All Phenotype Data
6 figures from Bammens et al., 2015
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With tmem165 Human Ortholog
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
Associated With tmem165 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR049555 GDT1-like, conserved site
Family IPR001727 GDT1-like
Domain Details Per Protein
Protein Length GDT1-like GDT1-like, conserved site
UniProtKB:Q8JJ62 305
Transcripts
Genome Browsers
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA tmem165-201 (1) Ensembl 2,163 nt
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