Homo sapiens Gene: DGCR6
Summary
InnateDB Gene IDBG-1186.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DGCR6
Gene Name DiGeorge syndrome critical region gene 6
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000183628
Encoded Proteins
DiGeorge syndrome critical region gene 6
DiGeorge syndrome critical region gene 6
DiGeorge syndrome critical region gene 6
DiGeorge syndrome critical region gene 6
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. The product of this gene shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the gamma-1 subunit of human laminin. This gene is a candidate for involvement in DiGeorge syndrome pathology and in schizophrenia. [provided by RefSeq, Nov 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 22:18906028-18914238
Strand Forward strand
Band q11.21
Transcripts
ENST00000331444 ENSP00000331681
ENST00000413981 ENSP00000402409
ENST00000427407 ENSP00000397633
ENST00000436645
ENST00000483718 ENSP00000467483
ENST00000480608 ENSP00000466276
ENST00000477156
ENST00000608842 ENSP00000476388
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 64 experimentally validated interaction(s) in this database.
Experimentally validated
Total 64 [view]
Protein-Protein 61 [view]
Protein-DNA 3 [view]
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:0007155 cell adhesion
GO:0009887 organ morphogenesis
Cellular Component
GO:0005578 proteinaceous extracellular matrix
GO:0005634 nucleus
Orthologs
No orthologs found for this gene
Cross-References
SwissProt Q14129
TrEMBL G5E9J8 K7ELY4 K7EPQ2 Q6FGH4 X5D7D2
UniProt Splice Variant
Entrez Gene 8214
UniGene Hs.474185 Hs.641881
RefSeq NM_005675
HUGO HGNC:2846
OMIM 601279
CCDS CCDS13753
HPRD
IMGT
EMBL AC007326 AF228707 AK315115 BC047039 CH471176 CR456434 CR542133 KJ534820 KJ535003 X96484
GenPept AAH47039 AAK15584 AHW56460 AHW56642 BAG37572 CAA65339 CAG30320 CAG46930 EAX03075 EAX03077
RNA Seq Atlas 102724770 8214