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ACTG1P23 actin gamma 1 pseudogene 23 [ Homo sapiens (human) ]

Gene ID: 442097, updated on 10-Oct-2023

Summary

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Official Symbol
ACTG1P23provided by HGNC
Official Full Name
actin gamma 1 pseudogene 23provided by HGNC
Primary source
HGNC:HGNC:51503
See related
Ensembl:ENSG00000230362 AllianceGenome:HGNC:51503
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See ACTG1P23 in Genome Data Viewer
Location:
3q26.31
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (175977486..175978575, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (178772459..178773548, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (175695274..175696363, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene N-acetylated alpha-linked acidic dipeptidase like 2 Neighboring gene NAALADL2 antisense RNA 1 Neighboring gene uncharacterized LOC124909459 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr3:175540382-175540932 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:175552923-175553428 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:175623336-175623892 Neighboring gene NANOG hESC enhancer GRCh37_chr3:175703537-175704064 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:175733597-175734192 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:175734193-175734788 Neighboring gene NANOG hESC enhancer GRCh37_chr3:175778986-175779524 Neighboring gene EI24 pseudogene 1 Neighboring gene EI24 pseudogene 6

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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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.

Genomic

  1. NG_022227.2 

    Range
    101..1190
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    175977486..175978575 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    178772459..178773548 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases