Homo sapiens Gene: DONSON
Summary
InnateDB Gene IDBG-2423.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DONSON
Gene Name downstream neighbor of SON
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000159147
Encoded Proteins
downstream neighbor of SON
downstream neighbor of SON
downstream neighbor of SON
downstream neighbor of SON
downstream neighbor of SON
downstream neighbor of SON
downstream neighbor of SON
downstream neighbor of SON
downstream neighbor of SON
downstream neighbor of SON
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene lies downstream of the SON gene and spans 10 kb on chromosome 21. The function of this gene is unknown. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 21:33559542-33588708
Strand Reverse strand
Band q22.11
Transcripts
ENST00000303113 ENSP00000304716
ENST00000303071 ENSP00000307143
ENST00000453626 ENSP00000394276
ENST00000457359 ENSP00000415191
ENST00000417871 ENSP00000392014
ENST00000444517 ENSP00000392405
ENST00000442660 ENSP00000408788
ENST00000437395 ENSP00000399535
ENST00000432378 ENSP00000398329
ENST00000440810 ENSP00000401082
ENST00000460557
ENST00000462566
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0007275 multicellular organismal development
GO:0008150 biological_process
Cellular Component
GO:0005575 cellular_component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL C9JSP0
UniProt Splice Variant
Entrez Gene 29980
UniGene Hs.436341
RefSeq NM_017613
HUGO HGNC:2993
OMIM 611428
CCDS CCDS13632
HPRD 09926
IMGT
EMBL AP000303 AP000304
GenPept
RNA Seq Atlas 29980