DRG2

DRG2
Identifiers
Aliases	DRG2, developmentally regulated GTP binding protein 2
External IDs	OMIM: 602986; MGI: 1342307; HomoloGene: 1061; GeneCards: DRG2; OMA:DRG2 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	18,107,970 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	60,359,580 bp
RNA expression pattern
	Top expressed in
	granulocyte; ; right lobe of liver; ; anterior pituitary; ; apex of heart; ; body of uterus; ; gastrocnemius muscle; ; right ovary; ; right lobe of thyroid gland; ; left ovary; ; canal of the cervix;
	Top expressed in
	otic vesicle; ; morula; ; neural layer of retina; ; internal carotid artery; ; otic placode; ; external carotid artery; ; saccule; ; tail of embryo; ; epiblast; ; ventricular zone;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	nucleotide binding; GTP binding; protein binding; RNA binding; GTPase activity; hydrolase activity; metal ion binding;
Cellular component	membrane; mitochondrion; intracellular membrane-bounded organelle; nucleoplasm; cytoplasm; cytosol; nucleus;
Biological process	signal transduction; cytoplasmic translation;
	Sources:Amigo / QuickGO
Orthologs
	1819
	13495
	ENSG00000108591
	ENSMUSG00000020537
	P55039
	Q9QXB9
	NM_001388; NM_001330144
	NM_021354
	NP_001317073; NP_001379
	NP_067329
	Wikidata
View/Edit Human	View/Edit Mouse

Developmentally-regulated GTP-binding protein 2 is a protein that in humans is encoded by the DRG2 gene.^[5]^[6]^[7]

The DRG2 gene encodes the developmentally regulated GTP-binding protein 2, a name derived from the fact that it shares significant similarity to known GTP-binding proteins. DRG2 was identified because it is expressed in normal fibroblasts but not in SV40-transformed fibroblasts. Read-through transcripts containing this gene and a downstream gene have been identified, but they are not thought to encode a fusion protein. This gene is located within the Smith-Magenis syndrome region on chromosome 17.^[7]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000108591 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000020537 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Schenker T, Trueb B (Jun 1998). "Assignment of the gene for a developmentally regulated GTP-binding protein (DRG2) to human chromosome bands 17p13→p12 by in situ hybridization". Cytogenet Cell Genet. 79 (3–4): 274–5. doi:10.1159/000134741. PMID 9605870.
^ Schenker T, Lach C, Kessler B, Calderara S, Trueb B (Nov 1994). "A novel GTP-binding protein which is selectively repressed in SV40 transformed fibroblasts". J Biol Chem. 269 (41): 25447–53. doi:10.1016/S0021-9258(18)47271-7. PMID 7929244.
^ ^a ^b "Entrez Gene: DRG2 developmentally regulated GTP binding protein 2".

Sprang SR (1998). "G proteins, effectors and GAPs: structure and mechanism". Curr. Opin. Struct. Biol. 7 (6): 849–56. doi:10.1016/S0959-440X(97)80157-1. PMID 9434906.
Liang Y, Wang A, Belyantseva IA, et al. (2000). "Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2". Genomics. 61 (3): 243–58. doi:10.1006/geno.1999.5976. PMID 10552926.
Li B, Trueb B (2000). "DRG represents a family of two closely related GTP-binding proteins". Biochim. Biophys. Acta. 1491 (1–3): 196–204. doi:10.1016/s0167-4781(00)00025-7. PMID 10760581.
Vlangos CN, Das P, Patel PI, Elsea SH (2000). "Assignment of developmentally regulated GTP-binding protein (DRG2) to human chromosome band 17p11.2 with somatic cell hybrids and localization to the Smith-Magenis syndrome critical interval". Cytogenet. Cell Genet. 88 (3–4): 283–5. doi:10.1159/000015539. PMID 10828610. S2CID 32462696.
Bi W, Yan J, Stankiewicz P, et al. (2002). "Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17p11.2 and the Syntenic Region of the Mouse". Genome Res. 12 (5): 713–28. doi:10.1101/gr.73702. PMC 186594. PMID 11997338.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Song H, Kim SI, Ko MS, et al. (2005). "Overexpression of DRG2 increases G2/M phase cells and decreases sensitivity to nocodazole-induced apoptosis". J. Biochem. 135 (3): 331–5. doi:10.1093/jb/mvh040. PMID 15113831.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.

This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000108591 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000020537 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid9605870-5] Schenker T, Trueb B (Jun 1998). "Assignment of the gene for a developmentally regulated GTP-binding protein (DRG2) to human chromosome bands 17p13→p12 by in situ hybridization". Cytogenet Cell Genet. 79 (3–4): 274–5. doi:10.1159/000134741. PMID 9605870.

[pmid7929244-6] Schenker T, Lach C, Kessler B, Calderara S, Trueb B (Nov 1994). "A novel GTP-binding protein which is selectively repressed in SV40 transformed fibroblasts". J Biol Chem. 269 (41): 25447–53. doi:10.1016/S0021-9258(18)47271-7. PMID 7929244.

[entrez-7] "Entrez Gene: DRG2 developmentally regulated GTP binding protein 2".

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References

Further reading