Gene

tmem38b

ID
ZDB-GENE-040426-807
Name
transmembrane protein 38B
Symbol
tmem38b Nomenclature History
Previous Names
  • zgc:55815
Type
protein_coding_gene
Location
Chr: 21 Mapping Details/Browsers
Description
Predicted to have potassium channel activity. Predicted to be involved in potassium ion transmembrane transport. Predicted to localize to endoplasmic reticulum; endoplasmic reticulum membrane; and integral component of membrane. Human ortholog(s) of this gene implicated in osteogenesis imperfecta type 14. Orthologous to human TMEM38B (transmembrane protein 38B).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from Tonelli et al., 2023
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
4 figures from Tonelli et al., 2023
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With tmem38b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
osteogenesis imperfecta type 14 Alliance Osteogenesis imperfecta, type XIV 615066
Associated With tmem38b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR007866 TRIC channel
Domain Details Per Protein
Protein Length TRIC channel
UniProtKB:Q7ZVP8 289
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations