| Name |
|---|
PKP4P1 Geneplakophilin 4 pseudogene 1 |
PKP2P1 Geneplakophilin 2 pseudogene 1 |
PKP4 Geneplakophilin 4 Armadillo-like proteins are characterized by a series of armadillo repeats, first defined in the Drosophila 'armadillo' gene product, that are typically 42 to 45 amino acids in length. These proteins can be divided into subfamilies based on their number of repeats, their overall sequence similarity, and the dispersion of the repeats throughout their sequences. Members of the p120(ctn)/plakophilin subfamily of Armadillo-like proteins, including CTNND1, CTNND2, PKP1, PKP2, PKP4, and ARVCF. PKP4 may be a component of desmosomal plaque and other adhesion plaques and is thought to be involved in regulating junctional plaque organization and cadherin function. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2015] |
PKP3 Geneplakophilin 3 This gene encodes a member of the arm-repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This protein may act in cellular desmosome-dependent adhesion and signaling pathways. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014] |
PKP2 Geneplakophilin 2 This gene encodes a member of the arm-repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This gene may regulate the signaling activity of beta-catenin and is required to maintain transcription of genes that control intracellular calcium cycling including ryanodine receptor 2, ankyrin-B, triadin, and calcium channel, voltage-dependent, L type, alpha 1C. Mutations in this gene are associated with different inherited cardiac conditions including Arrythmogenic Cardiomyopathy, Brugada Syndrome, and Idiopathic Ventricular Fibrillation. A processed pseudogene with high similarity to this gene has been mapped to chromosome 12p13. [provided by RefSeq, May 2022] |
PKP1 Geneplakophilin 1 This gene encodes a member of the arm-repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This protein may be involved in molecular recruitment and stabilization during desmosome formation. Mutations in this gene have been associated with the ectodermal dysplasia/skin fragility syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010] |
plakophilin Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term plakophilin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Plakophilin-4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Plakophilin-4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Plakophilin-3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Plakophilin-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Plakophilin-1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Plakophilin-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Plakophilin/Delta catenin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Plakophilin/Delta catenin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Epidermolysis bullosa simplex due to plakophilin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Epidermolysis bullosa simplex due to plakophilin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |