GPR139 - G protein-coupled receptor 139 Gene

Also Known as PGR3; GPRg1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 124274

About GPR139

Cytogenetic location: 16p12.3 Genomic coordinates (GRCh38): 16:20,028,239-20,073,890 (from NCBI)

This gene has 2 transcripts (splice variants), 335 orthologues and 1 paralogue. Low expression observed in reference dataset.

Summary

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]

GPR139 Products (2)

mRNA Protein Name
NM_001002911.4 NP_001002911.1 probable G-protein coupled receptor 139 isoform 1
NM_001318483.1 NP_001305412.1 probable G-protein coupled receptor 139 isoform 2
Biological Process GO Annotation Evidence References Source
acts upstream of or within G protein-coupled receptor signaling pathway IDA
IDA: Inferred from direct assay
15845401 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GPR139 Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (44 - 285)

  • 0
  • 100
  • 200
  • 300
  • 353 a.a.
Protein Preferred Names Protein Names

probable G-protein coupled receptor 139

  • G protein-coupled receptor PGR3

  • g(q)-coupled orphan receptor GPRg1

Related Diseases

Diseases Alias
Isolated Growth Hormone Deficiency, Type Ib
  • Isolated Growth Hormone Deficiency Type Ib

  • IGHD1B

  • Ighd Ib

  • Growth Hormone Deficiency, Isolated, Type Ib

  • Congenital Ighd Type Ib

  • Congenital Isolated Gh Deficiency Type Ib

  • Congenital Isolated Growth Hormone Deficiency Type Ib

  • Dwarfism Of Sindh

  • Pituitary Dwarfism I

  • Isolated Growth Hormone Deficiency Type 1b

  • Ighd 1b

  • Growth Hormone Deficiency, Isolated, 1b

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris GPR139 VGNC VGNC:41400
Macaca mulatta GPR139 VGNC VGNC:104730
Rattus norvegicus GPR139 RGD RGD:1311729
Mus musculus GPR139 MGD MGI:2685341
Felis catus GPR139 VGNC VGNC:80578
Bos taurus GPR139 VGNC VGNC:29553
Others GPR139 NCBI