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DOC2GP double C2 domain gamma, pseudogene [ Homo sapiens (human) ]

Gene ID: 390213, updated on 13-May-2022

Summary

Official Symbol
DOC2GPprovided by HGNC
Official Full Name
double C2 domain gamma, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:37962
See related
AllianceGenome:HGNC:37962
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
Predicted to act upstream of or within spontaneous neurotransmitter secretion. [provided by Alliance of Genome Resources, Apr 2022]
Expression
Low expression observed in reference dataset See more
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Genomic context

See DOC2GP in Genome Data Viewer
Location:
11q13.2
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (67613524..67615664, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (67608210..67610350, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (67380995..67383135, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene NDUFV1 divergent transcript Neighboring gene NADH:ubiquinone oxidoreductase core subunit V1 Neighboring gene uncharacterized LOC124902696 Neighboring gene nudix hydrolase 8

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Other Names

  • double C2, gamma pseudogene
  • double C2-like domains, gamma, pseudogene

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.

RNA

  1. NR_033791.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AP003385

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_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    67613524..67615664 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    67608210..67610350 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)