Homo sapiens Gene: NSUN5P2
Summary
InnateDB Gene IDBG-19311.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NSUN5P2
Gene Name NOP2/Sun domain family, member 5 pseudogene 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000106133
Encoded Proteins
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Feb 2010] This gene shares high sequence similarity with the genes WBSCR20A and WBSCR20C; these three genes are the products of gene duplication during evolution. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Feb 2010]
Gene Information
Type transcribed_unprocessed_pseudogene
Genomic Location Chromosome 7:72947581-72954790
Strand Reverse strand
Band q11.23
Transcripts
ENST00000388955
ENST00000444583
ENST00000457352
ENST00000485741
ENST00000602348
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Orthologs
No orthologs found for this gene
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene
RefSeq
HUGO
OMIM
CCDS
HPRD 15657
IMGT
EMBL
GenPept
RNA Seq Atlas