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Gene : FRZB Homo sapiens

Name  ? frizzled related protein Cytological Location  2q32.1
Brief Description  frizzled related protein
Description  The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female-specific osteoarthritis (OA) susceptibility. [provided by RefSeq, Apr 2010]
  • synonyms:
  • FRZB,
  • FRP-3,
  • FRE,
  • FRE,
  • OTTHUMG00000132597,
  • hFIZ,
  • OS1,
  • FZRB,
  • SFRP3,
  • NM_001463,
  • FRITZ,
  • SFRP3,
  • SRFP3,
  • SRFP3,
  • FRZB-PEN,
  • FRITZ,
  • FZRB,
  • HGNC:3959,
  • uc002upa.4,
  • hFIZ,
  • FRP-3,
  • FRZB-1,
  • secreted frizzled-related protein 3,
  • FRZB1,
  • FRZB-1,
  • U24163,
  • FRZB1,
  • FRZB-PEN
  • identifiers:
  • 2487,
  • ENSG00000162998,
  • FRZB

Genome feature

Region: gene ? Length: 33363  
Location: 2:182833275-182866637 reverse strand Cyto location: 2q32.1


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

3753 SN Ps

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results