DRG2

DRG2
Developmentally regulated GTP binding protein 2
Identifiers
Symbols DRG2;
External IDs OMIM602986 MGI1342307 HomoloGene1061 GeneCards: DRG2 Gene
RNA expression pattern
PBB GE DRG2 203267 s at tn.png
PBB GE DRG2 203268 s at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 1819 13495
Ensembl ENSG00000108591 ENSMUSG00000020537
UniProt P55039 Q5SX94
RefSeq (mRNA) NM_001388 NM_021354.1
RefSeq (protein) NP_001379 NP_067329.1
Location (UCSC) Chr 17:
17.99 – 18.01 Mb
Chr 11:
60.27 – 60.28 Mb
PubMed search [1] [2]

Developmentally-regulated GTP-binding protein 2 is a protein that in humans is encoded by the DRG2 gene.[1][2][3]

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.[3]

References

  1. ^ 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. 
  2. ^ 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. PMID 7929244. 
  3. ^ a b "Entrez Gene: DRG2 developmentally regulated GTP binding protein 2". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1819. 

Further reading




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  • Potocki-Lupski syndrome — (PTLS), also known as dup(17)p11.2p11.2 syndrome, trisomy 17p11.2 or duplication 17p11.2 syndrome, is a contiguous gene syndrome involving the microduplication of band 11.2 on the short arm of human chromosome 17 (17p11.2).[1] The duplication was …   Wikipedia

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