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PPM1D

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Protein-coding gene in the species Homo sapiens
PPM1D
Identifiers
AliasesPPM1D, PP2C-DELTA, WIP1, protein phosphatase, Mg2+/Mn2+ dependent 1D, IDDGIP, JDVS, WIP1 protein, human, PPM1D protein, human
External IDsOMIM: 605100; MGI: 1858214; HomoloGene: 31185; GeneCards: PPM1D; OMA:PPM1D - orthologs
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)
Chromosome 17 (human)Genomic location for PPM1DGenomic location for PPM1D
Band17q23.2Start60,600,193 bp
End60,666,280 bp
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)
Chromosome 11 (mouse)Genomic location for PPM1DGenomic location for PPM1D
Band11 C|11 51.34 cMStart85,202,070 bp
End85,237,892 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • secondary oocyte

  • amniotic fluid

  • ventricular zone

  • gonad

  • placenta

  • ganglionic eminence

  • mucosa of sigmoid colon

  • jejunal mucosa

  • germinal epithelium

  • Achilles tendon
Top expressed in
  • seminiferous tubule

  • spermatid

  • genital tubercle

  • fetal liver hematopoietic progenitor cell

  • tail of embryo

  • spermatocyte

  • zygote

  • lobe of cerebellum

  • medial ganglionic eminence

  • cerebellar vermis
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

8493

53892

Ensembl

ENSG00000170836

ENSMUSG00000020525

UniProt

O15297

Q9QZ67

RefSeq (mRNA)

NM_003620

NM_016910

RefSeq (protein)

NP_003611

NP_058606

Location (UCSC)Chr 17: 60.6 – 60.67 MbChr 11: 85.2 – 85.24 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Protein phosphatase 1D is an enzyme that in humans is encoded by the PPM1D gene.

The protein encoded by this gene is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative regulators of cell stress response pathways. The expression of this gene is induced in a p53-dependent manner in response to various environmental stresses. While being induced by tumor suppressor protein TP53/p53, this phosphatase negatively regulates the activity of p38 MAP kinase (MAPK/p38) through which it reduces the phosphorylation of p53, and in turn suppresses p53-mediated transcription and apoptosis. This phosphatase thus mediates a feedback regulation of p38-p53 signaling that contributes to growth inhibition and the suppression of stress induced apoptosis. This gene is located in a chromosomal region known to be amplified in breast cancer. The amplification of this gene has been detected in both breast cancer cell line and primary breast tumors, which suggests a role of this gene in cancer development. Pathogenic variants in exons 5-6 in the PPM1D gene can cause the neurodevelopmental disorder known as Jansen-de Vries Syndrome (JdVS).

Interactions

PPM1D has been shown to interact with CDC5L.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000170836Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000020525Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Fiscella M, Zhang H, Fan S, Sakaguchi K, Shen S, Mercer WE, Vande Woude GF, O'Connor PM, Appella E (July 1997). "Wip1, a novel human protein phosphatase that is induced in response to ionizing radiation in a p53-dependent manner". Proc Natl Acad Sci U S A. 94 (12): 6048–53. Bibcode:1997PNAS...94.6048F. doi:10.1073/pnas.94.12.6048. PMC 20998. PMID 9177166.
  6. ^ "Entrez Gene: PPM1D protein phosphatase 1D magnesium-dependent, delta isoform".
  7. Wojcik, Monica H; Srivastava, Siddharth; Agrawal, Pankaj B; Balci, Tugce B; Callewaert, Bert; Calvo, Pier Luigi; Carli, Diana; Caudle, Michelle; Colaiacovo, Samantha; Cross, Laura; Demetriou, Kalliope; Drazba, Katy; Dutra-Clarke, Marina; Edwards, Matthew; Genetti, Casie A (July 2023). "Jansen-DeVries Syndrome: Expansion of the PPM1D Clinical and Phenotypic Spectrum in 34 Families". American Journal of Medical Genetics. Part A. 191 (7): 1900–1910. doi:10.1002/ajmg.a.63226. ISSN 1552-4825. PMC 10330231. PMID 37183572.
  8. Ajuh, P; Kuster B; Panov K; Zomerdijk J C; Mann M; Lamond A I (December 2000). "Functional analysis of the human CDC5L complex and identification of its components by mass spectrometry". EMBO J. 19 (23): 6569–81. doi:10.1093/emboj/19.23.6569. ISSN 0261-4189. PMC 305846. PMID 11101529.

Further reading

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