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Gene : GPR179 Homo sapiens

Name  ? G protein-coupled receptor 179 Cytological Location  17q12
Brief Description  G protein-coupled receptor 179
Description  This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E. [provided by RefSeq, Apr 2012]
  • synonyms:
  • GPR179,
  • NM_001004334,
  • GPR179,
  • OTTHUMG00000188545,
  • HGNC:31371,
  • GPR158-like 1,
  • GPR158L,
  • CSNB1E,
  • uc032gkv.1,
  • GPR158L1,
  • GPR158L1,
  • CSNB1E
  • identifiers:
  • 440435,
  • ENSG00000277399,
  • GPR179

Genome feature

Region: gene ? Length: 19386  
Location: 17:38324571-38343956 reverse strand Cyto location: 17q12


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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

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

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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

3753 SN Ps

5 Cross References

16 Data Sets

8 Homologues

0 Located Features

97 Rna Seq Results