Gene

crtap

ID
ZDB-GENE-040426-2619
Name
cartilage associated protein
Symbol
crtap Nomenclature History
Previous Names
  • wu:fb47h01
  • zgc:85621
Type
protein_coding_gene
Location
Chr: 19 Mapping Details/Browsers
Description
Predicted to be involved in peptidyl-proline hydroxylation to 3-hydroxy-L-proline. Predicted to localize to endoplasmic reticulum. Human ortholog(s) of this gene implicated in osteogenesis imperfecta type 7. Is expressed in notochord; otic vesicle; pectoral fin; periderm; and pharyngeal arch. Orthologous to human CRTAP (cartilage associated protein).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
7 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
5 figures from Tonelli et al., 2020
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With crtap Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
osteogenesis imperfecta type 7 Alliance Osteogenesis imperfecta, type VII 610682
Associated With crtap Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Homologous_superfamily IPR011990 Tetratricopeptide-like helical domain superfamily
Domain Details Per Protein
Protein Length Tetratricopeptide-like helical domain superfamily
UniProtKB:Q6NWL3 396
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