U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

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

Gene ID: 25786, updated on 13-May-2022

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
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See DGCR11 in Genome Data Viewer
Location:
22q11.21
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (19046162..19048375, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (19421486..19423698, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (19033675..19035888, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene DiGeorge syndrome critical region gene 5 Neighboring gene family with sequence similarity 246 member C (gene/pseudogene) Neighboring gene CA15 pseudogene 1 Neighboring gene DiGeorge syndrome critical region gene 2 Neighboring gene ribosomal protein L28 pseudogene Neighboring gene uncharacterized LOC124905078

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

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

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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.

RNA

  1. NR_024157.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AK098432
    Related
    ENST00000609958.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    19046162..19048375 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    19421486..19423698 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)