PARD3

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PARD3
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)
RefSeq (protein)
Location (UCSC)Chr 10: 34.11 – 34.82 MbChr 8: 127.79 – 128.34 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Partitioning defective 3 homolog is a protein that in humans is encoded by the PARD3 gene.[5][6]

Function

PARD proteins, which were first identified in C. elegans, are essential for asymmetric cell division and polarized growth, whereas CDC42 (MIM 116952) mediates the establishment of cell polarity. The CDC42 GTPase, which is controlled by nucleotide exchange factors (GEFs; see MIM 606057) and GTPase-activating proteins (GAPs; see MIM 604980), interacts with a large set of effector proteins that typically contain a CDC42/RAC (MIM 602048)-interactive binding (CRIB) domain.[supplied by OMIM][6]

Interactions

PARD3 has been shown to

interact
with:

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000148498Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025812Ensembl, 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. S2CID 27139234
    .
  6. ^ a b "Entrez Gene: PARD3 par-3 partitioning defective 3 homolog (C. elegans)".
  7. ^
    PMID 12953056
    .
  8. .
  9. .

Further reading


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