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Desmoglein-4 is a protein that in humans is encoded by the DSG4 gene. List of conditions caused by problems with junctional proteins GRCh38: Ensembl release...
Click to read more »Type OMIM Gene Locus LAH1 607903 DSG4 18q12 LAH2 604379 LIPH 3q27 LAH3 611452 P2RY5 13q14.12-q14.2...
Click to read more »family of desmosomal cadherins consisting of proteins DSG1, DSG2, DSG3, and DSG4. They play a role in the formation of desmosomes that join cells to one another...
Click to read more »(2006-06-01). "An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis". Journal...
Click to read more »HGNC:3048; Q02413 4560 DSG2 HGNC:3049; Q14126 4561 DSG3 HGNC:3050; P32926 4562 DSG4 HGNC:21307; Q86SJ6 4563 DSN1 HGNC:16165; Q9H410 4564 DSP HGNC:3052; P15924...
Click to read more »(placental): P-cadherins are found in the placenta. Desmoglein (DSG1, DSG2, DSG3, DSG4) Desmocollin (DSC1, DSC2, DSC3) Protocadherins are the largest mammalian...
Click to read more »(2006). "An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis". Journal...
Click to read more »3; 611452; P2RY5 Hypotrichosis, localized, autosomal recessive; 607903; DSG4 Hypotrichosis-lymphedema-telangiectasia syndrome; 607823; SOX18 Hypouricemia...
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