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Gene : CRTAP Homo sapiens

Name  ? cartilage associated protein Cytological Location  3p22.3
Brief Description  cartilage associated protein
Description  The protein encoded by this gene is similar to the chicken and mouse CRTAP genes. The encoded protein is a scaffolding protein that may influence the activity of at least one member of the cytohesin/ARNO family in response to specific cellular stimuli. Defects in this gene are associated with osteogenesis imperfecta, a connective tissue disorder characterized by bone fragility and low bone mass. [provided by RefSeq, Jul 2008]
  • synonyms:
  • AJ006470,
  • OI7,
  • P3H5,
  • leprecan-like 3,
  • CRTAP,
  • LEPREL3,
  • uc003cfl.5,
  • CASP,
  • CASP,
  • OTTHUMG00000130746,
  • P3H5,
  • NM_006371,
  • prolyl 3-hydroxylase family member 5 (non-enzymatic),
  • HGNC:2379,
  • identifiers:
  • 10491,
  • ENSG00000170275,

Genome feature

Region: gene ? Length: 33760  
Location: 3:33114014-33147773 Cyto location: 3p22.3

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Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3740 SNPs

5 Cross References

19 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results