Gene

rps17

ID
ZDB-GENE-040426-1852
Name
ribosomal protein S17
Symbol
rps17 Nomenclature History
Previous Names
  • zgc:77702
Type
protein_coding_gene
Location
Chr: 7 Mapping Details/Browsers
Description
Predicted to be a structural constituent of ribosome. Predicted to be involved in translation. Predicted to localize to ribosome. Is expressed in several structures, including alar plate midbrain region; digestive system; eye; immature eye; and midbrain. Human ortholog(s) of this gene implicated in Diamond-Blackfan anemia 4. Orthologous to human RPS17 (ribosomal protein S17).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
6 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 rps17 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Diamond-Blackfan anemia 4 Alliance Diamond-Blackfan anemia 4 612527
Associated With rps17 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR018273 Ribosomal protein S17e, conserved site
Family IPR001210 Ribosomal protein S17e
Homologous_superfamily IPR036401 Ribosomal protein S17e-like superfamily
Domain Details Per Protein
Protein Length Ribosomal protein S17e Ribosomal protein S17e, conserved site Ribosomal protein S17e-like superfamily
UniProtKB:Q6P6F0 134
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