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    ZSWIM6 zinc finger SWIM-type containing 6 [ Homo sapiens (human) ]

    Gene ID: 57688, updated on 10-Dec-2024

    Summary

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    Official Symbol
    ZSWIM6provided by HGNC
    Official Full Name
    zinc finger SWIM-type containing 6provided by HGNC
    Primary source
    HGNC:HGNC:29316
    See related
    Ensembl:ENSG00000130449 MIM:615951; AllianceGenome:HGNC:29316
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    AFND; NEDMAGA
    Summary
    The protein encoded by this gene contains a zinc finger SWI2/SNF2 and MuDR (SWIM) domain. Proteins with SWIM domains have been found in a diverse number of species and are predicted to interact with DNA or proteins. Mutations in this gene result in acromelic frontonasal dysostosis. [provided by RefSeq, Apr 2017]
    Expression
    Ubiquitous expression in gall bladder (RPKM 6.8), brain (RPKM 6.4) and 25 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See ZSWIM6 in Genome Data Viewer
    Location:
    5q12.1
    Exon count:
    16
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (61332258..61546172)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (62151402..62365278)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (60628085..60841999)

    Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105378993 Neighboring gene uncharacterized LOC105378994 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr5:60626175-60626745 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16045 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16046 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16047 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16048 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16049 Neighboring gene DEAD-box helicase 25 pseudogene Neighboring gene family with sequence similarity 133 member B pseudogene Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr5:60703838-60705037 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:60711419-60712045 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr5:60712046-60712673 Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:60712674-60713300 Neighboring gene ribosomal protein L3 pseudogene 6 Neighboring gene basic proline-rich protein Neighboring gene long intergenic non-protein coding RNA 3122 Neighboring gene uncharacterized LOC101928651 Neighboring gene heat shock protein family D (Hsp60) member 1 pseudogene 22

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

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    Related articles in PubMed

    1. A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations. Palmer EE, et al. Am J Hum Genet, 2017 Dec 7. PMID 29198722, Free PMC Article
    2. Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism. Twigg SR, et al. Clin Genet, 2016 Sep. PMID 26706854, Free PMC Article
    3. Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Cha MY, et al. Sci Rep, 2022 Aug 15. PMID 35970861, Free PMC Article
    4. Altered gene expression in the subdivisions of the amygdala of Fyn-deficient mice as revealed by laser capture microdissection and mKIAA cDNA array analysis. Kai N, et al. Brain Res, 2006 Feb 16. PMID 16427614
    5. Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis. Smith JD, et al. Am J Hum Genet, 2014 Aug 7. PMID 25105228, Free PMC Article

    See all (21) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations.
      Title: Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations.
    2. This study builds support for a key role for ZSWIM6 in neuronal development and function, in addition to its putative roles in limb and craniofacial development, and provides a striking example of different variants in the same gene leading to distinct phenotypes.
      Title: A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations.
    3. A single recurrent heterozygous missense substitution in ZSWIM6, encoding a protein of unknown function, was previously shown to underlie this disorder in four unrelated cases. Here we describe four additional individuals from three families, comprising two sporadic subjects (one of whom had no limb malformation) and a mildly affected female with a severely affected son
      Title: Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism.
    4. Exome sequencing of one trio and two unrelated probands revealed the same heterozygous variant (c.3487C>T [p. Arg1163Trp])associated with acromelic frontonasal dysostosis in a highly conserved protein domain of ZSWIM6; this variant has not been seen in the 1000 Genomes data, dbSNP, or the Exome Sequencing Project
      Title: Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.
    Submit: New GeneRIF Correction

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    Associated conditions

    Description Tests
    Acromelic frontonasal dysostosis
    MedGen: C1863616 OMIM: 603671 GeneReviews: Not available
    		Compare labs
    Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features
    MedGen: C4693405 OMIM: 617865 GeneReviews: Not available
    		Compare labs

    EBI GWAS Catalog

    Description
    Biological insights from 108 schizophrenia-associated genetic loci.
    EBI GWAS Catalog
    Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
    EBI GWAS Catalog
    Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
    EBI GWAS Catalog

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • KIAA1577, DKFZp779P0344

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables zinc ion binding IEA
    Inferred from Electronic Annotation
    more info
    		  
    Process Evidence Code Pubs
    involved_in striatal medium spiny neuron differentiation ISS
    Inferred from Sequence or Structural Similarity
    more info
    		  
    Component Evidence Code Pubs
    part_of Cul2-RING ubiquitin ligase complex IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  

    General protein information

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    Preferred Names
    zinc finger SWIM domain-containing protein 6
    Names
    zinc finger, SWIM domain containing 6

    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_053150.1 RefSeqGene

      Range
      4986..218900
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_020928.2 → NP_065979.1  zinc finger SWIM domain-containing protein 6

      See identical proteins and their annotated locations for NP_065979.1

      Status: REVIEWED

      Source sequence(s)
      AA740254, AB046797, AC008836, AC122718, AW136453, BF750632, BF751445
      Consensus CDS
      CCDS47215.1
      UniProtKB/Swiss-Prot
      Q9HCJ5
      Related
      ENSP00000252744.5, ENST00000252744.6

    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_000005.10 Reference GRCh38.p14 Primary Assembly

      Range
      61332258..61546172
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047417453.1 → XP_047273409.1  zinc finger SWIM domain-containing protein 6 isoform X3

    2. XM_024446139.2 → XP_024301907.1  zinc finger SWIM domain-containing protein 6 isoform X1

    3. XM_017009677.2 → XP_016865166.1  zinc finger SWIM domain-containing protein 6 isoform X2

    4. XM_047417454.1 → XP_047273410.1  zinc finger SWIM domain-containing protein 6 isoform X4

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060929.1 Alternate T2T-CHM13v2.0

      Range
      62151402..62365278
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054353016.1 → XP_054208991.1  zinc finger SWIM domain-containing protein 6 isoform X1

    2. XM_054353018.1 → XP_054208993.1  zinc finger SWIM domain-containing protein 6 isoform X3

    3. XM_054353017.1 → XP_054208992.1  zinc finger SWIM domain-containing protein 6 isoform X2

    4. XM_054353019.1 → XP_054208994.1  zinc finger SWIM domain-containing protein 6 isoform X4

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q9HCJ5.2 GenPept UniProtKB/Swiss-Prot:Q9HCJ5

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

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