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* 300513

G PROTEIN-COUPLED RECEPTOR 119; GPR119


Alternative titles; symbols

G PROTEIN-COUPLED RECEPTOR 2; GPCR2


HGNC Approved Gene Symbol:GPR119

Cytogenetic location:Xq26.1   Genomic coordinates(GRCh38) :X:130,379,449-130,385,674 (from NCBI)


TEXT

Description

GPR119 is a member of the rhodopsin family of G protein-coupled receptors (GPRs) (Fredriksson et al., 2003).


Cloning and Expression

By searching databases for GPRs containing no introns in the coding region,Takeda et al. (2002) identified GPR119, which they designated GPCR2. The deduced protein shares 27% homology with dopamine receptor-1 (see126449). RT-PCR detected ubiquitous GPR119 expression.

By searching databases for sequences similar to rhodopsin-like GPRs,Fredriksson et al. (2003) identified mouse and human GPR119. The deduced 335-amino acid proteins assume a classic 7-transmembrane (TM) topology and share 82% amino acid identity. They contain the characteristic DRY motif in the intracellular side of TM3 and an NSxxNPxxY motif in TM7.


Gene Structure

Takeda et al. (2002) andFredriksson et al. (2003) determined that the coding regions of the mouse and human GPR119 genes are derived from a single exon.


Mapping

By genomic sequence analysis,Fredriksson et al. (2003) mapped the GPR119 gene to chromosome Xq26.1. They mapped the mouse Gpr119 gene to the X chromosome.


REFERENCES

  1. Fredriksson, R., Hoglund, P. J., Gloriam, D. E. I., Lagerstrom, M. C., Schioth, H. B.Seven evolutionarily conserved human rhodopsin G protein-coupled receptors lacking close relatives. FEBS Lett. 554: 381-388, 2003. [PubMed:14623098,related citations] [Full Text]

  2. Takeda, S., Kadowaki, S., Haga, T., Takaesu, H., Mitaku, S.Identification of G protein-coupled receptor genes from the human genome sequence. FEBS Lett. 520: 97-101, 2002. Note: Erratum: FEBS Lett. 523: 257 only, 2002. [PubMed:12044878,related citations] [Full Text]


Creation Date:
Patricia A. Hartz : 11/23/2004
joanna : 05/27/2013
mgross : 11/23/2004

* 300513

G PROTEIN-COUPLED RECEPTOR 119; GPR119


Alternative titles; symbols

G PROTEIN-COUPLED RECEPTOR 2; GPCR2


HGNC Approved Gene Symbol: GPR119

Cytogenetic location: Xq26.1   Genomic coordinates(GRCh38) : X:130,379,449-130,385,674(from NCBI)


TEXT

Description

GPR119 is a member of the rhodopsin family of G protein-coupled receptors (GPRs) (Fredriksson et al., 2003).


Cloning and Expression

By searching databases for GPRs containing no introns in the coding region, Takeda et al. (2002) identified GPR119, which they designated GPCR2. The deduced protein shares 27% homology with dopamine receptor-1 (see 126449). RT-PCR detected ubiquitous GPR119 expression.

By searching databases for sequences similar to rhodopsin-like GPRs, Fredriksson et al. (2003) identified mouse and human GPR119. The deduced 335-amino acid proteins assume a classic 7-transmembrane (TM) topology and share 82% amino acid identity. They contain the characteristic DRY motif in the intracellular side of TM3 and an NSxxNPxxY motif in TM7.


Gene Structure

Takeda et al. (2002) and Fredriksson et al. (2003) determined that the coding regions of the mouse and human GPR119 genes are derived from a single exon.


Mapping

By genomic sequence analysis, Fredriksson et al. (2003) mapped the GPR119 gene to chromosome Xq26.1. They mapped the mouse Gpr119 gene to the X chromosome.


REFERENCES

  1. Fredriksson, R., Hoglund, P. J., Gloriam, D. E. I., Lagerstrom, M. C., Schioth, H. B.Seven evolutionarily conserved human rhodopsin G protein-coupled receptors lacking close relatives. FEBS Lett. 554: 381-388, 2003. [PubMed: 14623098] [Full Text: https://doi.org/10.1016/s0014-5793(03)01196-7]

  2. Takeda, S., Kadowaki, S., Haga, T., Takaesu, H., Mitaku, S.Identification of G protein-coupled receptor genes from the human genome sequence. FEBS Lett. 520: 97-101, 2002. Note: Erratum: FEBS Lett. 523: 257 only, 2002. [PubMed: 12044878] [Full Text: https://doi.org/10.1016/s0014-5793(02)02775-8]


Creation Date:
Patricia A. Hartz : 11/23/2004

Edit History:
joanna : 05/27/2013
mgross : 11/23/2004



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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2026 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2026 Johns Hopkins University.
Printed: Feb. 20, 2026

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