Homo sapiens Gene: PURG
Summary
InnateDB Gene IDBG-16066.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PURG
Gene Name purine-rich element binding protein G
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000172733
Encoded Proteins
purine-rich element binding protein G
purine-rich element binding protein G
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The exact function of this gene is not known, however, its encoded product is highly similar to purine-rich element binding protein A. The latter is a DNA-binding protein which binds preferentially to the single strand of the purine-rich element termed PUR, and has been implicated in the control of both DNA replication and transcription. This gene lies in close proximity to the Werner syndrome gene, but on the opposite strand, on chromosome 8p11. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 8:30995802-31033715
Strand Reverse strand
Band p12
Transcripts
ENST00000339382 ENSP00000345168
ENST00000475541 ENSP00000418721
ENST00000523392 ENSP00000466881
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 1 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0044822 poly(A) RNA binding
Biological Process
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
Non-SSD Ortholog
Possible paralog/unusual divergence/ gene prediction error
Not yet available
Non-SSD Ortholog
Possible paralog/unusual divergence/ gene prediction error
Cross-References
SwissProt Q9UJV8
TrEMBL K7ENC1
UniProt Splice Variant
Entrez Gene 29942
UniGene Hs.373778
RefSeq NM_001015508 NM_013357 XM_005273483 XM_005273484
HUGO HGNC:17930
OMIM
CCDS CCDS34878 CCDS6081
HPRD
IMGT
EMBL AC008066 AC084736 AF195513 AY077841 BC106708
GenPept AAF03900 AAI06709 AAL77218
RNA Seq Atlas 29942