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    ZNF559-ZNF177 ZNF559-ZNF177 readthrough [ Homo sapiens (human) ]

    Gene ID: 100529215, updated on 2-Nov-2024

    Summary

    Official Symbol
    ZNF559-ZNF177provided by HGNC
    Official Full Name
    ZNF559-ZNF177 readthroughprovided by HGNC
    Primary source
    HGNC:HGNC:42964
    See related
    Ensembl:ENSG00000270011 AllianceGenome:HGNC:42964
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Summary
    This locus represents naturally occurring read-through transcription between the neighboring zinc finger protein 559 (ZNF559) and zinc finger protein 177 (ZNF177) genes on chromosome 19. Alternative splicing results in multiple transcript variants, which encode the ZNF177 protein due to either leaky scanning by ribosomes, or absence of the ZNF559 start codon. [provided by RefSeq, Jan 2011]
    Expression
    Broad expression in testis (RPKM 5.0), ovary (RPKM 3.1) and 22 other tissues See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See ZNF559-ZNF177 in Genome Data Viewer
    Location:
    19p13.2
    Exon count:
    16
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (9324179..9382617)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (9450390..9508854)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (9434855..9493293)

    Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 7 subfamily H member 1 pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr19:9406829-9407424 Neighboring gene zinc finger protein 699 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10037 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 13927 Neighboring gene Sharpr-MPRA regulatory region 15409 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 13928 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 10038 Neighboring gene zinc finger protein 559 Neighboring gene UBXN2A pseudogene 1 Neighboring gene zinc finger protein 177 Neighboring gene uncharacterized LOC112268250 Neighboring gene zinc finger protein 266 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 13929

    Genomic regions, transcripts, and products

    Expression

    • 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

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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.

    mRNA and Protein(s)

    1. NM_001172650.3NP_001166121.1  zinc finger protein 177 isoform b

      See identical proteins and their annotated locations for NP_001166121.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) contains alternate exon structure in the 5' UTR, uses an alternate splice site that causes a frameshift in the 3' coding region, and lacks a segment of the 3' UTR, compared to variant 4. The resulting isoform (b) has a distinct and longer C-terminus, compared to isoform c. A non-read-through variant of the downstream ZNF177 gene, as represented by GeneID:7730, also encodes isoform b.
      Source sequence(s)
      AC011451, BC034489
      UniProtKB/Swiss-Prot
      Q13360
      Related
      ENSP00000445323.1, ENST00000541595.6
      Conserved Domains (4) summary
      smart00349
      Location:1470
      KRAB; krueppel associated box
      COG5048
      Location:87282
      COG5048; FOG: Zn-finger [General function prediction only]
      sd00017
      Location:126146
      ZF_C2H2; C2H2 Zn finger [structural motif]
      pfam13465
      Location:279303
      zf-H2C2_2; Zinc-finger double domain
    2. NM_001202425.1NP_001189354.1  zinc finger protein 177 isoform c

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) represents the longer transcript but encodes the shorter isoform (c).
      Source sequence(s)
      AC011451, BC034489, U37251
      UniProtKB/TrEMBL
      V9H066
      Related
      ENSP00000413568.2, ENST00000446085.8
      Conserved Domains (2) summary
      smart00349
      Location:1470
      KRAB; krueppel associated box
      pfam01352
      Location:1453
      KRAB; KRAB box
    3. NM_001384659.1NP_001371588.1  zinc finger protein 177 isoform a

      Status: VALIDATED

      Source sequence(s)
      AC011451
      UniProtKB/Swiss-Prot
      B4DY57, E9PDG0, I3L0I4, Q13360, Q96ER2
      Conserved Domains (4) summary
      smart00349
      Location:1470
      KRAB; krueppel associated box
      COG5048
      Location:212442
      COG5048; FOG: Zn-finger [General function prediction only]
      sd00017
      Location:286306
      ZF_C2H2; C2H2 Zn finger [structural motif]
      pfam13465
      Location:439463
      zf-H2C2_2; Zinc-finger double domain

    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
      9324179..9382617
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060943.1 Alternate T2T-CHM13v2.0

      Range
      9450390..9508854
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)