Gene

xnp-1

Species
Caenorhabditis elegans
Symbol
xnp-1
Name
human XNP gene related 1
Synonyms
  • B0041.7
  • CELE_B0041.7
Biotype
protein coding gene
Automated Description
Predicted to enable ATP-dependent chromatin remodeler activity and transcription coregulator activity. Involved in several processes, including embryo development; gonad development; and vulval development. Predicted to be active in nucleus. Is expressed in body wall musculature; germ line; hermaphrodite gonad; nervous system; and vulval precursor cell. Used to study intellectual disability. Human ortholog(s) of this gene implicated in X-linked mental retardation-hypotonic facies syndrome-1; alpha thalassemia-X-linked intellectual disability syndrome; alpha-thalassemia myelodysplasia syndrome; high grade glioma; and lung small cell carcinoma. Orthologous to human ATRX (ATRX chromatin remodeler).
WB Description
xnp-1 encodes an ATP-dependent DNA helicase of the SNF2 family that is orthologous to human XNP/ATR-X, which is associated with a number of X-linked mental retardation syndromes; in C. elegans, xnp-1 activity is required at high temperatures for embryogenesis, somatic gonad development, fertility, and vulval morphogenesis; in addition, animals doubly mutant for xnp-1 and lin-35/Rb, hpl-2/HP1, or nucleosome remodelling and histone deacetylase (NuRD) complex members such as lin-53 and let-418, display larval arrest with growth cessation but continued cell proliferation; xnp-1 is also required, with lin-35/Rb and hpl-2/HP1, for proper regulation of transgene expression; xnp-1 mRNA, detectable in embryos and the germline by in situ hybridization, is expressed at highest levels in embryos with decreasing levels seen in successive larval stages; xnp-1 transcriptional reporter fusions exhibit strong expression beginning at mid-embryogenesis but fading by embryonic morphogenesis; at hatching, expression is observed in all dividing cells including the P lineage, and at later larval stages expression is observed in the vulval precursor cells.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR45797
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Paralogy

Function - GO Annotations

Pathways

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Phenotypes

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    Disease Associations

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    Alleles and Variants

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      Transgenic Alleles

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      (carrying the transgene)
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          WBcel235
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          Sequence Details

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          Expression

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          Molecular Interactions

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            Genetic Interactions

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