Gene

tmem63a

ID
ZDB-GENE-041210-107
Name
transmembrane protein 63A
Symbol
tmem63a Nomenclature History
Previous Names
  • si:ch211-117l16.1 (1)
Type
protein_coding_gene
Location
Chr: 4 Mapping Details/Browsers
Description
Predicted to have calcium activated cation channel activity. Predicted to localize to plasma membrane. Human ortholog(s) of this gene implicated in hypomyelinating leukodystrophy. Orthologous to human TMEM63A (transmembrane protein 63A).
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 tmem63a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Leukodystrophy, hypomyelinating, 19, transient infantile 618688
Associated With tmem63a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR003864 Calcium-dependent channel, 7TM region, putative phosphate
Domain IPR027815 10TM putative phosphate transporter, cytosolic domain
Domain IPR032880 Calcium permeable stress-gated cation channel 1, N-terminal transmembrane domain
Family IPR026957 CSC1-like protein 1
Domain Details Per Protein
Protein Length 10TM putative phosphate transporter, cytosolic domain Calcium-dependent channel, 7TM region, putative phosphate Calcium permeable stress-gated cation channel 1, N-terminal transmembrane domain CSC1-like protein 1
UniProtKB:A4QP59 802
UniProtKB:F1R745 802
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