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    ANAPC1P2 ANAPC1 pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 285074, updated on 17-Sep-2024

    Summary

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    Official Symbol
    ANAPC1P2provided by HGNC
    Official Full Name
    ANAPC1 pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:54708
    See related
    Ensembl:ENSG00000285793 AllianceGenome:HGNC:54708
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Ubiquitous expression in bone marrow (RPKM 19.3), spleen (RPKM 9.0) and 25 other tissues See more
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    Genomic context

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    See ANAPC1P2 in Genome Data Viewer
    Location:
    2p11.2
    Exon count:
    11
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (87030675..87076413, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (87035895..87081642, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (87257798..87303536, complement)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene RANBP2 like and GRIP domain containing 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:87169373-87170136 Neighboring gene NADH:ubiquinone oxidoreductase subunit B4 pseudogene 5 Neighboring gene plasminogen like B1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11722 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11723 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11724 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11725 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:87303801-87304306 Neighboring gene tRNA-Pro (anticodon AGG) 4-1 Neighboring gene ANAPC1 pseudogene 3

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: HPA RNA-seq normal tissues 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

    Bibliography

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    Related articles in PubMed

    1. Lineage-specific gene duplication and loss in human and great ape evolution. Fortna A, et al. PLoS Biol, 2004 Jul. PMID 15252450, Free PMC Article
    2. Complete sequencing and characterization of 21,243 full-length human cDNAs. Ota T, et al. Nat Genet, 2004 Jan. PMID 14702039
    3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

    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)

    Genotypes

    General gene information

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    Markers

    Other Names

    • anaphase promoting complex subunit 1 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_026846.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC125232, BC069048, BM454994, BX353812
      Related
      ENST00000648819.1

    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_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      87030675..87076413 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      87035895..87081642 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001012626.1: Suppressed sequence

      Description
      NM_001012626.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
    Nucleotide Protein
    Heading Accession and Version

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