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Gene : PAX9 Homo sapiens

Name  ? paired box 9 Cytological Location  14q13.3
Brief Description  paired box 9
description  This gene is a member of the paired box (PAX) family of transcription factors. Members of this gene family typically contain a paired box domain, an octapeptide, and a paired-type homeodomain. These genes play critical roles during fetal development and cancer growth. Mice lacking this gene exhibit impaired development of organs, musculature and the skeleton, including absent and abnormally developed teeth, and neonatal lethality. Mutations in the human gene are associated with selective tooth agenesis-3. [provided by RefSeq, Sep 2015]
  • synonyms:
  • OTTHUMG00000140251,
  • paired box gene 9,
  • HGNC:8623,
  • uc001wty.5,
  • NM_006194,
  • STHAG3,
  • PAX9,
  • AJ238381
  • identifiers:
  • 5083,
  • ENSG00000198807,
  • PAX9

Genome feature

Region: gene ? Length: 20240  
Location: 14:36657568-36677807 Cyto location: 14q13.3


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Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

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

Homologue Displayer

Gene --> Orthologues

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

440 SN Ps

5 Cross References

19 Data Sets

15 Homologues

0 Located Features

90 Rna Seq Results