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Search references for PARD3. Phrases containing PARD3
See searches and references containing PARD3!PARD3
Protein-coding gene in the species Homo sapiens
Partitioning defective 3 homolog is a protein that in humans is encoded by the PARD3 gene. PARD proteins, which were first identified in C. elegans, are essential
PARD3
Mammalian protein found in Homo sapiens
tumor progressiveness. Nectin-3 has been shown to interact with: MLLT4, PARD3, PTPRM. GRCh38: Ensembl release 89: ENSG00000177707 – Ensembl, May 2017
Nectin-3
Protein-coding gene in the species Homo sapiens
with: Centaurin, alpha 1, FRS2, Glyceraldehyde 3-phosphate dehydrogenase, PARD3, Phosphoinositide-dependent kinase-1, SMG1 (gene), Sequestosome 1, KRAS
PRKCI
Protein-coding gene in the species Homo sapiens
associating to cell polarity protein PARD3 (PAR-3), together with JAM3. JAM2 has been shown to interact with PARD3. It also interacts with the integrin
JAM2
Topics referred to by the same term
Partitioning defective 3 homolog, a protein that in humans is encoded by the PARD3 gene 3PAR This disambiguation page lists articles associated with the same
PAR3
Protein family
MAST4 MCSP MLLT4 MPDZ MPP1 MPP2 MPP3 MPP4 MPP5 MPP6 MPP7 MYO18A NHERF1 NOS1 PARD3 PARD6A PARD6B PARD6G PDLIM1 PDLIM2 PDLIM3 PDLIM4 PDLIM5 PDLIM7 PDZD11 PDZD2
PDZ_domain
Cells forming the neural tube wall during embryogenesis
required for the generation of neuroblasts. Another tight junction protein, PARD3, remains at the apical side of the cell co-localizing with N-cadherin and
Neuroepithelial_cell
Protein family
proteins like PAR-3 and ZO-1. JAM-3 has also been shown to interact with PARD3 (partitioning defective 3 homolog).[citation needed] JAMs serve many different
Junctional_adhesion_molecule
Q86WK9 11706 PAQR8 HGNC:15708; Q8TEZ7 11707 PAQR9 HGNC:30131; Q6ZVX9 11708 PARD3 HGNC:16051; Q8TEW0 11709 PARD3B HGNC:14446; Q8TEW8 11710 PARD6A HGNC:15943;
List of human protein-coding genes 6
List_of_human_protein-coding_genes_6
Protein-coding gene in the species Homo sapiens
for another member of this family. JAM3 has been shown to interact with PARD3. Loss-of-function mutations in this gene cause a rare syndrome - autosomal
JAM3
PARD3
PARD3
PARD3
PARD3
Surname or Lastname
English
English : variant spelling of Harcombe, a habitational name from either of two places in Devon and Hampshire so named, probably from Old English hara ‘hare’ + cumb ‘valley’, or from various minor places named with this word, such as Harcomb Bottom in Devon and Gloucestershire, both named with Old English heorot ‘hart’ + cumb.
Girl/Female
Latin
Blackbird.
Girl/Female
Indian, Sanskrit
Story; Narration
Boy/Male
Indian
Islamic thinker, Saint, Beautiful
Girl/Female
Australian, Irish
Sorrowful
Boy/Male
Hindu
Girl/Female
Spanish
Bright; glowing white.
Boy/Male
Hindu, Indian
Attachment
Girl/Female
Indian
Well born
Girl/Female
Hindu
Princess
PARD3
PARD3
PARD3
PARD3
PARD3