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. Author manuscript; available in PMC: 2021 Sep 1.
Published in final edited form as: Biochim Biophys Acta Biomembr. 2020 May 3;1862(9):183329. doi: 10.1016/j.bbamem.2020.183329

Table 1:

Mouse genetic studies reveal important roles for desmosomal proteins in development and homeostasis.

Gene Expression Lethality Observed Defects References
Dsg1 Knockout Perinatal Lethal epidermal water loss, severe blistering [124]
Dsg2 Knockout Embryonic Lethal Pre-implantation lethality, potentially non-desmosomal role [125]
Suprabasal Epidermal Misexpression Not Lethal Hyperproliferation, abnormal differentiation, barrier defects [28]
Dsg3 Knockout Not Lethal Separated keratinocytes, weakened desmosomal adhesion in oral mucosa [126]
Suprabasal Epidermal Misexpression Not Lethal Hyperproliferation, abnormal differentiation, barrier defects [127]
Dsc1 Knockout Not Lethal Epidermal hyperproliferation, loss of cell-cell adhesion [128]
Dsc3 Knockout Embryonic Lethal Post-implantation lethality, potentially non-desmosomal role [129]
Epidermal Conditional Not Lethal Epidermal fragility, hair loss [130]
Suprabasal Epidermal Misexpression Not Lethal Hyperproliferation, abnormal differentiation, barrier defects [123]
PG Knockout Embryonic Lethal Heart defects, skin fragility [131]
Pkp1 Knockout Postnatal Lethality Epidermal fragility, tight junction defects, growth defects [132]
DP Knockout Embryonic Lethal Die at E6.5 [133]
Epidermal Conditional Perinatal Lethal Severe skin fragility, disrupted barrier function [134]