DGCR6

Protein DGCR6 is a protein that in humans is encoded by the DGCR6 gene.[3][4]

DGCR6
Identifiers
Aliases	DGCR6, DiGeorge syndrome critical region gene 6
External IDs	OMIM: 601279 HomoloGene: 136000 GeneCards: DGCR6
Gene location (Human) Chr. Chromosome 22 (human)[1] Band 22q11.21|22q11 Start 18,906,028 bp[1] End 18,914,238 bp[1]
RNA expression pattern More reference expression data
Gene ontology Molecular function • molecular function Cellular component • cell nucleus • extracellular matrix Biological process • animal organ morphogenesis • cell adhesion Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	8214	n/a
Ensembl	ENSG00000183628	n/a
UniProt	Q14129 Q6FGH4	n/a
RefSeq (mRNA)	NM_005675	n/a
RefSeq (protein)	NP_001355171	n/a
Location (UCSC)	Chr 22: 18.91 – 18.91 Mb	n/a
PubMed search	[2]	n/a
Wikidata
View/Edit Human

DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. This gene product shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the human laminin gamma-1 chain, which upon polymerization with alpha- and beta-chains forms the laminin molecule. Laminin binds to cells through interaction with a receptor and has functions in cell attachment, migration, and tissue organization during development. This gene could be a candidate for involvement in the DiGeorge syndrome pathology by playing a role in neural crest cell migration into the third and fourth pharyngeal pouches, the structures from which derive the organs affected in DiGeorge syndrome.[4]

References

1. GRCh38: Ensembl release 89: ENSG00000183628 - Ensembl, May 2017
2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
3. Demczuk S, Thomas G, Aurias A (Jun 1997). "Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes". Hum Mol Genet. 5 (5): 633–8. doi:10.1093/hmg/5.5.633. PMID 8733130.
4. "Entrez Gene: DGCR6 DiGeorge syndrome critical region gene 6".

Further reading

• Edelmann L, Stankiewicz P, Spiteri E, et al. (2001). "Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus". Genome Res. 11 (2): 208–17. doi:10.1101/gr.gr-1431r. PMC 311013. PMID 11157784.
• Liu H, Heath SC, Sobin C, et al. (2002). "Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia". Proc. Natl. Acad. Sci. U.S.A. 99 (6): 3717–22. doi:10.1073/pnas.042700699. PMC 122590. PMID 11891283.
• Chakravarti A (2002). "A compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility". Proc. Natl. Acad. Sci. U.S.A. 99 (8): 4755–6. doi:10.1073/pnas.092158299. PMC 122660. PMID 11959925.
• Wistow G, Bernstein SL, Wyatt MK, et al. (2002). "Expressed sequence tag analysis of human retina for the NEIBank Project: retbindin, an abundant, novel retinal cDNA and alternative splicing of other retina-preferred gene transcripts". Mol. Vis. 8: 196–204. PMID 12107411.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Collins JE, Wright CL, Edwards CA, et al. (2005). "A genome annotation-driven approach to cloning the human ORFeome". Genome Biol. 5 (10): R84. doi:10.1186/gb-2004-5-10-r84. PMC 545604. PMID 15461802.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Pfuhl T, Dürr M, Spurk A, et al. (2005). "Biochemical characterisation of the proteins encoded by the DiGeorge critical region 6 (DGCR6) genes". Hum. Genet. 117 (1): 70–80. doi:10.1007/s00439-005-1267-2. PMID 15821931.