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ACTG1P21 actin gamma 1 pseudogene 21 [ Homo sapiens (human) ]

Gene ID: 100131291, updated on 17-Sep-2024

Summary

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Official Symbol
ACTG1P21provided by HGNC
Official Full Name
actin gamma 1 pseudogene 21provided by HGNC
Primary source
HGNC:HGNC:51501
See related
Ensembl:ENSG00000232672 AllianceGenome:HGNC:51501
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 ACTG1P21 in Genome Data Viewer
Location:
1p31.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (77773868..77774879, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (77612677..77613688, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (78239553..78240564, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene zinc finger ZZ-type containing 3 Neighboring gene RNA, 7SL, cytoplasmic 370, pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:78127789-78128288 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1216 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1002 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:78149296-78150069 Neighboring gene ubiquitin specific peptidase 33 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1218 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1004 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1219 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1220 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:78241322-78241846 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1221 Neighboring gene RNA, 5S ribosomal pseudogene 21 Neighboring gene mitoguardin 1 Neighboring gene axin interactor, dorsalization associated pseudogene

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_022723.1 

    Range
    101..1112
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    77773868..77774879 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    77612677..77613688 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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