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Gene : FSHR Homo sapiens

Name  ? follicle stimulating hormone receptor Cytological Location  2p16.3
Brief Description  follicle stimulating hormone receptor
Description  The protein encoded by this gene belongs to family 1 of G-protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
  • synonyms:
  • ODG1,
  • OTTHUMG00000129259,
  • LGR1,
  • FSHR1,
  • ODG1,
  • HGNC:3969,
  • FSHRO,
  • uc002rww.4,
  • FSHR,
  • LGR1,
  • FSHRO,
  • NM_000145
  • identifiers:
  • 2492,
  • ENSG00000170820,
  • FSHR

Genome feature

Region: gene ? Length: 201367  
Location: 2:48953161-49154527 reverse strand Cyto location: 2p16.3


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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 --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

3 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

906 SN Ps

5 Cross References

18 Data Sets

11 Homologues

0 Located Features

97 Rna Seq Results