Gene

zgc:101715

ID
ZDB-GENE-040912-59
Name
zgc:101715
Symbol
zgc:101715 Nomenclature History
Previous Names
  • c19orf12b2 (1)
Type
protein_coding_gene
Location
Chr: 7 Mapping Details/Browsers
Description
Predicted to localize to several cellular components, including cytosol; endoplasmic reticulum; and mitochondrial membrane. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 43 and neurodegeneration with brain iron accumulation 4. Orthologous to human C19orf12 (chromosome 19 open reading frame 12).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
4 figures from 2 publications
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 zgc:101715 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
hereditary spastic paraplegia 43 Alliance ?Spastic paraplegia 43, autosomal recessive 615043
neurodegeneration with brain iron accumulation 4 Alliance Neurodegeneration with brain iron accumulation 4 614298
Associated With zgc:101715 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR033369 Protein C19orf12
Domain Details Per Protein
Protein Length Protein C19orf12
UniProtKB:Q66ID9 141
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
Citations