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    Hells helicase, lymphoid specific [ Mus musculus (house mouse) ]

    Gene ID: 15201, updated on 11-Apr-2024

    Summary

    Official Symbol
    Hellsprovided by MGI
    Official Full Name
    helicase, lymphoid specificprovided by MGI
    Primary source
    MGI:MGI:106209
    See related
    Ensembl:ENSMUSG00000025001 AllianceGenome:MGI:106209
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Mus musculus
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
    Also known as
    LSH; Lysh; PASG; YFK8; E130115I21Rik
    Summary
    Enables chromatin binding activity. Involved in DNA methylation-dependent heterochromatin assembly; maintenance of DNA methylation; and pericentric heterochromatin assembly. Acts upstream of or within several processes, including DNA methylation; cellular response to leukemia inhibitory factor; and negative regulation of intrinsic apoptotic signaling pathway. Located in nucleus and pericentric heterochromatin. Is expressed in several structures, including central nervous system; gut; neural retina; reproductive system; and thymus. Human ortholog(s) of this gene implicated in immunodeficiency-centromeric instability-facial anomalies syndrome 4. Orthologous to human HELLS (helicase, lymphoid specific). [provided by Alliance of Genome Resources, Apr 2022]
    Expression
    Biased expression in CNS E11.5 (RPKM 12.2), liver E14 (RPKM 8.5) and 10 other tissues See more
    Orthologs
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    Genomic context

    Location:
    19 C3; 19 33.57 cM
    Exon count:
    23
    Annotation release Status Assembly Chr Location
    RS_2024_02 current GRCm39 (GCF_000001635.27) 19 NC_000085.7 (38913282..38958914)
    108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) 19 NC_000085.6 (38930262..38970470)

    Chromosome 19 - NC_000085.7Genomic Context describing neighboring genes Neighboring gene NOC3 like DNA replication regulator Neighboring gene TBC1D12: TBC1 domain family, member 12 Neighboring gene STARR-seq mESC enhancer starr_46100 Neighboring gene STARR-seq mESC enhancer starr_46102 Neighboring gene cytochrome P450, family 2, subfamily c, polypeptide 52, pseudogene Neighboring gene STARR-seq mESC enhancer starr_46105 Neighboring gene STARR-seq mESC enhancer starr_46106 Neighboring gene cytochrome P450, family 2, subfamily c, polypeptide 55

    Genomic regions, transcripts, and products

    Expression

    • Project title: Mouse ENCODE transcriptome data
    • Description: RNA profiling data sets generated by the Mouse ENCODE project.
    • BioProject: PRJNA66167
    • Publication: PMID 25409824
    • Analysis date: n/a

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Variation

    Alleles

    Alleles of this type are documented at Mouse Genome Informatics  (MGI)
    • Gene trapped (1) 
    • Targeted (6)  1 citation
    • Endonuclease-mediated (1) 

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by MGI

    Function Evidence Code Pubs
    enables ATP binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables ATP-dependent chromatin remodeler activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables chromatin binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables chromatin binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables helicase activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables hydrolase activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables nucleotide binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in DNA methylation-dependent heterochromatin formation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in DNA methylation-dependent heterochromatin formation IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    acts_upstream_of apoptotic process IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    acts_upstream_of_or_within cell cycle IEA
    Inferred from Electronic Annotation
    more info
     
    acts_upstream_of_or_within cell division IEA
    Inferred from Electronic Annotation
    more info
     
    acts_upstream_of_or_within cellular response to leukemia inhibitory factor IEP
    Inferred from Expression Pattern
    more info
    PubMed 
    acts_upstream_of_or_within chromatin remodeling IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    acts_upstream_of_or_within chromosomal DNA methylation maintenance following DNA replication IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    acts_upstream_of_or_within heterochromatin formation IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in kidney development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    acts_upstream_of_or_within lymphocyte differentiation TAS
    Traceable Author Statement
    more info
    PubMed 
    involved_in lymphocyte proliferation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in lymphocyte proliferation IEP
    Inferred from Expression Pattern
    more info
    PubMed 
    acts_upstream_of_or_within multicellular organism development IEA
    Inferred from Electronic Annotation
    more info
     
    acts_upstream_of_or_within negative regulation of apoptotic process IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in negative regulation of gene expression via chromosomal CpG island methylation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in negative regulation of gene expression via chromosomal CpG island methylation IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    acts_upstream_of_or_within negative regulation of intrinsic apoptotic signaling pathway IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in pericentric heterochromatin formation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in pericentric heterochromatin formation IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    acts_upstream_of_or_within urogenital system development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in chromosome, centromeric region IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    PubMed 
    part_of pericentric heterochromatin IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    part_of pericentric heterochromatin IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    lymphocyte-specific helicase
    Names
    proliferation-associated SNF2-like protein

    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_008234.3NP_032260.2  lymphocyte-specific helicase

      See identical proteins and their annotated locations for NP_032260.2

      Status: VALIDATED

      Source sequence(s)
      AF155210
      Consensus CDS
      CCDS29789.1
      UniProtKB/Swiss-Prot
      Q497T3, Q60848, Q8VDZ1, Q9CYV7
      Related
      ENSMUSP00000025965.6, ENSMUST00000025965.12
      Conserved Domains (2) summary
      PLN03142
      Location:204781
      PLN03142; Probable chromatin-remodeling complex ATPase chain; Provisional
      cd18009
      Location:203436
      DEXHc_HELLS_SMARCA6; DEXH-box helicase domain of HELLS

    RefSeqs of Annotated Genomes: GCF_000001635.27-RS_2024_02

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCm39 C57BL/6J

    Genomic

    1. NC_000085.7 Reference GRCm39 C57BL/6J

      Range
      38913282..38958914
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_006526699.5XP_006526762.1  lymphocyte-specific helicase isoform X1

      See identical proteins and their annotated locations for XP_006526762.1

      UniProtKB/Swiss-Prot
      Q497T3, Q60848, Q8VDZ1, Q9CYV7
      Conserved Domains (2) summary
      PLN03142
      Location:204781
      PLN03142; Probable chromatin-remodeling complex ATPase chain; Provisional
      cd18009
      Location:203436
      DEXHc_HELLS_SMARCA6; DEXH-box helicase domain of HELLS
    2. XM_006526700.4XP_006526763.1  lymphocyte-specific helicase isoform X2

      Conserved Domains (1) summary
      PLN03142
      Location:4437
      PLN03142; Probable chromatin-remodeling complex ATPase chain; Provisional