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    ZNF101P1 zinc finger protein 101 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 100419867, updated on 10-Oct-2023

    Summary

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    Official Symbol
    ZNF101P1provided by HGNC
    Official Full Name
    zinc finger protein 101 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:44940
    See related
    AllianceGenome:HGNC:44940
    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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    Location:
    10p12.1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (28339277..28341065, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (28370341..28372129, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (28628206..28629994, complement)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene MAGUK p55 scaffold protein 7 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2249 Neighboring gene microRNA 8086 Neighboring gene MPP7 divergent transcript Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2250 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3190 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3191 Neighboring gene small nucleolar RNA U3 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3192 Neighboring gene long intergenic non-protein coding RNA 2652 Neighboring gene ribosomal protein SA pseudogene 10

    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_025421.3 

      Range
      101..1889
      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_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      28339277..28341065 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      28370341..28372129 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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    Other Literature Sources
    Molecular Biology Databases