Gene

tmem106ba

ID
ZDB-GENE-040426-1336
Name
transmembrane protein 106Ba
Symbol
tmem106ba Nomenclature History
Previous Names
  • zgc:64013
Type
protein_coding_gene
Location
Chr: 15 Mapping Details/Browsers
Description
Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in hypomyelinating leukodystrophy. Is expressed in forerunner cell group and somite. Orthologous to human TMEM106B (transmembrane protein 106B).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
6 figures 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 tmem106ba Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
hypomyelinating leukodystrophy 16 Alliance Leukodystrophy, hypomyelinating, 16 617964
Associated With tmem106ba Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR048509 Transmembrane protein 106, C-terminal domain
Domain IPR048511 Transmembrane protein 106, N-terminal
Family IPR009790 Transmembrane protein 106
Domain Details Per Protein
Protein Length Transmembrane protein 106 Transmembrane protein 106, C-terminal domain Transmembrane protein 106, N-terminal
UniProtKB:F1QCQ2 256
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