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Gene : GPR139 Homo sapiens

Name  ? G protein-coupled receptor 139 Cytological Location  16p12.3
Brief Description  G protein-coupled receptor 139
Description  This gene encodes a member of the rhodopsin family of G-protein-coupled receptors. The encoded protein is almost exclusively expressed in the central nervous system. L-tryptophan and L-phenylalanine may act as the physiologic ligands of the encoded protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
  • synonyms:
  • uc002dgu.2,
  • HGNC:19995,
  • NM_001002911,
  • AY255545,
  • PGR3,
  • PGR3,
  • GPR139,
  • GPRg1,
  • OTTHUMG00000177690
  • identifiers:
  • 124274,
  • ENSG00000180269,
  • GPR139

Genome feature

Region: gene ? Length: 45652  
Location: 16:20028239-20073890 reverse strand Cyto location: 16p12.3


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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

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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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

6 SN Ps

4 Cross References

12 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results