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    ZNF71-SMIM17 ZNF71-SMIM17 readthrough (NMD candidate) [ Homo sapiens (human) ]

    Gene ID: 114818278, updated on 3-Mar-2026
    Gene symbol
    ZNF71-SMIM17
    Gene description
    ZNF71-SMIM17 readthrough (NMD candidate)
    See related
    Ensembl:ENSG00000293626
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Summary
    This gene represents a read-through transcript composed of ZNF71 and SMIM17 sequence. The transcripts are thought to be non-coding because they would be subject to nonsense-mediated mRNA decay (NMD). [provided by RefSeq, May 2019]
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    See ZNF71-SMIM17 in Genome Data Viewer
    Location:
    19q13.43
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2025_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (56595302..56657247)
    RS_2025_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (59689707..59751380)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (57106670..57168615)

    Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904777 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11070 Neighboring gene sialic acid binding Ig like lectin 31, pseudogene Neighboring gene zinc finger protein 71 Neighboring gene ReSE screen-validated silencer GRCh37_chr19:57128366-57128584 Neighboring gene Sharpr-MPRA regulatory region 15209 Neighboring gene small integral membrane protein 17 Neighboring gene uncharacterized LOC105372473 Neighboring gene zinc finger protein 835 Neighboring gene uncharacterized LOC105372472

    Go to nucleotide: Graphics FASTA GenBank

    GeneRIFs: Gene References Into Functions

    Review eQTL and phenotype association data in this region using PheGenI

    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

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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_163262.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC007228
      Related
      ENST00000716550.1

    2. NR_163263.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC007228

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2025_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
      56595302..56657247
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060943.1 Alternate T2T-CHM13v2.0

      Range
      59689707..59751380
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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