DGCR11 DiGeorge syndrome critical region gene 11 [Homo sapiens (human)] - Gene

Summary

Official Symbol: DGCR11provided by HGNC
Official Full Name: DiGeorge syndrome critical region gene 11provided by HGNC
Primary source: HGNC:HGNC:17226
See related: Ensembl:ENSG00000273311 AllianceGenome:HGNC:17226
Gene type: ncRNA
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: DGS-D
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Genomic context

Location:: 22q11.21

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	22	NC_000022.11 (19046162..19048375, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	22	NC_060946.1 (19421486..19423698, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	22	NC_000022.10 (19033675..19035888, complement)

Chromosome 22 - NC_000022.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

General gene information

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Markers

D8S2279 (e-PCR)
- UniSTS:473907

D13S116 (e-PCR)
- UniSTS:147007

SHGC-35943 (e-PCR)
- UniSTS:72260

D22S1633 (e-PCR)
- UniSTS:473980

SHGC-132562 (e-PCR)
- UniSTS:173949

D11S3114 (e-PCR)
- UniSTS:152207

D22S1661 (e-PCR)
- UniSTS:474032

RH78708 (e-PCR)
- UniSTS:79047

Other Names

DiGeorge syndrome critical region gene 11 (non-protein coding)
DiGeorge syndrome gene D

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.