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PSMC1P8 proteasome 26S subunit, ATPase 1 pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 390297, updated on 10-Oct-2023

Summary

Official Symbol
PSMC1P8provided by HGNC
Official Full Name
proteasome 26S subunit, ATPase 1 pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:39783
See related
Ensembl:ENSG00000256896 AllianceGenome:HGNC:39783
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

Location:
12p12.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (17383113..17384645, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (17259348..17260880, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (17536047..17537579, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 837, pseudogene Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 12:17286714 Neighboring gene ribosomal protein L7 pseudogene 40 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 12:17310310 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 12:17311674 Neighboring gene VISTA enhancer hs993 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 12:17327941 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:17485772-17486971 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_26385 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:17535474-17536673 Neighboring gene translocase of inner mitochondrial membrane 17B pseudogene 1 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_26433 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_26470 Neighboring gene VISTA enhancer hs605 Neighboring gene long intergenic non-protein coding RNA 2378

Genomic regions, transcripts, and products

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_021683.3 

    Range
    101..1633
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    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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    17383113..17384645 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    17259348..17260880 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)