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    ZNF887P zinc finger protein 887, pseudogene [ Homo sapiens (human) ]

    Gene ID: 100419709, updated on 10-Dec-2024

    Summary

    Official Symbol
    ZNF887Pprovided by HGNC
    Official Full Name
    zinc finger protein 887, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:38700
    See related
    AllianceGenome:HGNC:38700
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ZNF887
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    Genomic context

    See ZNF887P in Genome Data Viewer
    Location:
    19p13.2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (11648348..11652160)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (11776523..11780336)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (11759163..11762975)

    Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:11708237-11709235 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10124 Neighboring gene zinc finger protein 627 Neighboring gene MPRA-validated peak3358 silencer Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:11734453-11734953 Neighboring gene vomeronasal 2 receptor 12 pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10125 Neighboring gene heterogeneous nuclear ribonucleoprotein A1 pseudogene 10 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr19:11785131-11785688 Neighboring gene zinc finger protein 833, pseudogene

    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_024217.2 

      Range
      101..3913
      Download
      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_000019.10 Reference GRCh38.p14 Primary Assembly

      Range
      11648348..11652160
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060943.1 Alternate T2T-CHM13v2.0

      Range
      11776523..11780336
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)