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DGCR6

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Protein-coding gene in the species Homo sapiens
DGCR6
Identifiers
AliasesDGCR6, DiGeorge syndrome critical region gene 6
External IDsOMIM: 601279; HomoloGene: 136000; GeneCards: DGCR6; OMA:DGCR6 - orthologs
Gene location (Human)
Chromosome 22 (human)
Chr.Chromosome 22 (human)
Chromosome 22 (human)Genomic location for DGCR6Genomic location for DGCR6
Band22q11.21|22q11Start18,906,028 bp
End18,914,238 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • skeletal muscle tissue

  • muscle of thigh

  • gastrocnemius muscle

  • right hemisphere of cerebellum

  • right frontal lobe

  • Hypothalamus

  • anterior cingulate cortex

  • Amygdala

  • hippocampus proper

  • nucleus accumbens
    n/a
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
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 Mbn/a
PubMed searchn/a
Wikidata
View/Edit Human

Protein DGCR6 is a protein that in humans is encoded by the DGCR6 gene.

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.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000183628Ensembl, 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


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