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Gene : FZD9 Homo sapiens

Name  ? frizzled class receptor 9 Cytological Location  7q11.23
Brief Description  frizzled class receptor 9
Description  Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney. [provided by RefSeq, Jul 2008]
  • synonyms:
  • frizzled homolog 9 (Drosophila),
  • OTTHUMG00000023051,
  • U82169,
  • frizzled (Drosophila) homolog 9,
  • HGNC:4047,
  • CD349,
  • FZD3,
  • uc003tyb.4,
  • FZD9,
  • CD349,
  • frizzled family receptor 9,
  • FZD3,
  • frizzled 9, seven transmembrane spanning receptor,
  • NM_003508
  • identifiers:
  • 8326,
  • ENSG00000188763,
  • FZD9

Genome feature

Region: gene ? Length: 2343  
Location: 7:73433778-73436120 Cyto location: 7q11.23


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> GO terms.

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 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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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

161 SN Ps

5 Cross References

14 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results