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Gene : BBS9 Homo sapiens

Name  ? Bardet-Biedl syndrome 9 Cytological Location  7p14.3
Brief Description  Bardet-Biedl syndrome 9
Description  This gene is downregulated by parathyroid hormone in osteoblastic cells, and therefore is thought to be involved in parathyroid hormone action in bones. The exact function of this gene has not yet been determined. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jan 2017]
  • synonyms:
  • OTTHUMG00000128659,
  • C18,
  • PTHB1,
  • B1,
  • PTHB1,
  • NM_001033604,
  • BBS9,
  • uc003tdp.1,
  • D1,
  • parathyroid hormone responsive B1 gene,
  • B1,
  • HGNC:30000
  • identifiers:
  • 27241,
  • ENSG00000122507,
  • BBS9

Genome feature

Region: gene ? Length: 507995  
Location: 7:33129244-33637238 Cyto location: 7p14.3

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Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

Overlapping Features Displayer

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

Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



3756 SN Ps

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results