Gene

tmem106bb

ID
ZDB-GENE-050913-37
Name
transmembrane protein 106Bb
Symbol
tmem106bb Nomenclature History
Previous Names
  • zgc:114147
Type
protein_coding_gene
Location
Chr: 19 Mapping Details/Browsers
Description
Predicted to be involved in dendrite morphogenesis and lysosome localization. Predicted to localize to lysosomal membrane. Human ortholog(s) of this gene implicated in hypomyelinating leukodystrophy. Orthologous to human TMEM106B (transmembrane protein 106B).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
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 tmem106bb Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
hypomyelinating leukodystrophy 16 Alliance Leukodystrophy, hypomyelinating, 16 617964
Associated With tmem106bb Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR009790 Transmembrane protein 106
Domain Details Per Protein
Protein Length Transmembrane protein 106
UniProtKB:Z4YHQ6 267
UniProtKB:Q1LWC2 267
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