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    FAM153DP family with sequence similarity 153 member D, pseudogene [ Homo sapiens (human) ]

    Gene ID: 102724062, updated on 10-Oct-2023

    Summary

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    Official Symbol
    FAM153DPprovided by HGNC
    Official Full Name
    family with sequence similarity 153 member D, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:55022
    See related
    AllianceGenome:HGNC:55022
    Gene type
    pseudo
    RefSeq status
    MODEL
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Low expression observed in reference dataset See more
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    Genomic context

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    Location:
    16p11.2
    Exon count:
    15
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (32600346..32626108)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (33014797..33040542)

    Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene poly(A) binding protein cytoplasmic 1 pseudogene 13 Neighboring gene ATP binding cassette subfamily D member 1 pseudogene 3 Neighboring gene uncharacterized LOC107984013 Neighboring gene TP53 target 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
    • 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. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560, 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 (GRCh38)

    Genotypes

    NCBI Reference Sequences (RefSeq)

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    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_000016.10 Reference GRCh38.p14 Primary Assembly

      Range
      32600346..32626108
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_004837542.2 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060940.1 Alternate T2T-CHM13v2.0

      Range
      33014797..33040542
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_007087058.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version

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