Gene

mrps22

ID
ZDB-GENE-070615-31
Name
mitochondrial ribosomal protein S22
Symbol
mrps22 Nomenclature History
Previous Names
  • zgc:165596
Type
protein_coding_gene
Location
Chr: 15 Mapping Details/Browsers
Description
Predicted to be a structural constituent of ribosome. Predicted to localize to mitochondrial small ribosomal subunit. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 5 and ovarian dysgenesis 7. Orthologous to human MRPS22 (mitochondrial ribosomal protein S22).
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 mrps22 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
combined oxidative phosphorylation deficiency 5 Alliance Combined oxidative phosphorylation deficiency 5 611719
ovarian dysgenesis 7 Alliance Ovarian dysgenesis 7 618117
Associated With mrps22 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR019374 Small ribosomal subunit protein mS22
Domain Details Per Protein
Protein Length Small ribosomal subunit protein mS22
UniProtKB:A5PLF9 340
Transcripts
Genome Browsers
Type Name Annotation Method Has Havana Data Length (nt) Analysis
aberrant processed transcript mrps22-202 (1) Ensembl 559 nt
aberrant processed transcript mrps22-204 (1) Ensembl 892 nt
mRNA mrps22-201 (1) Ensembl 1,248 nt
mRNA mrps22-203 (1) Ensembl 370 nt
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