Gene

mrps16

ID
ZDB-GENE-041010-123
Name
mitochondrial ribosomal protein S16
Symbol
mrps16 Nomenclature History
Previous Names
  • fi21d03
  • wu:fi21d03
  • zgc:103459 (1)
Type
protein_coding_gene
Location
Chr: 11 Mapping Details/Browsers
Description
Predicted to be a structural constituent of ribosome. Predicted to be involved in translation. Predicted to localize to mitochondrial small ribosomal subunit. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 2. Is expressed in alar plate midbrain region; eye; immature eye; midbrain; and optic tectum. Orthologous to human MRPS16 (mitochondrial ribosomal protein S16).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
7 figures 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 mrps16 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
combined oxidative phosphorylation deficiency 2 Alliance Combined oxidative phosphorylation deficiency 2 610498
Associated With mrps16 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR000307 Small ribosomal subunit protein bS16
Homologous_superfamily IPR023803 Small ribosomal subunit protein bS16 domain superfamily
Domain Details Per Protein
Protein Length Small ribosomal subunit protein bS16 Small ribosomal subunit protein bS16 domain superfamily
UniProtKB:Q5XJB4 129
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