Gene

tmem107

ID
ZDB-GENE-040426-2294
Name
transmembrane protein 107
Symbol
tmem107 Nomenclature History
Previous Names
  • zgc:77926 (1)
Type
protein_coding_gene
Location
Chr: 14 Mapping Details/Browsers
Description
Predicted to be involved in non-motile cilium assembly and protein localization to ciliary transition zone. Predicted to localize to MKS complex. Human ortholog(s) of this gene implicated in Meckel syndrome 13 and orofaciodigital syndrome XVI. Orthologous to human TMEM107 (transmembrane protein 107).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure 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 tmem107 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Meckel syndrome 13 Alliance Meckel syndrome 13 617562
Meckel syndrome 13 Alliance ?Joubert syndrome 29 617562
orofaciodigital syndrome XVI Alliance Orofaciodigital syndrome XVI 617563
Associated With tmem107 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR029248 Transmembrane protein 107
Domain Details Per Protein
Protein Length Transmembrane protein 107
UniProtKB:Q6NZZ4 135
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