Associated Papers
Mutations within the predicted fragment-binding region of FAM83G/SACK1G abolish its interaction with the Ser/Thr kinase CK1α.
Utgés JS et al.
Open Biology, 2026
The contribution of native protein complexes to targeted protein degradation.
Glennie L et al.
Biorxiv : the Preprint Server for Biology, 2025
Expanding phenotypic insights of palmoplantar keratodermas based on novel FAM83G variants.
van Gisbergen MW et al.
The British Journal of Dermatology, 2025
Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G.
Mora-Gómez M et al.
Frontiers in Medicine, 2025
A novel FAM83G variant from palmoplantar keratoderma patient disrupts WNT signalling via loss of FAM83G-CK1α interaction.
Glennie L et al.
Open Biology, 2024
FAM83G/Fam83g genetic variants affect canine and murine hair formation.
Balmer P et al.
Experimental Dermatology, 2019
Pathogenic FAM83G palmoplantar keratoderma mutations inhibit the PAWS1:CK1α association and attenuate Wnt signalling.
Wu KZL et al.
Wellcome Open Research, 2019
The FAM83 family of proteins: from pseudo-PLDs to anchors for CK1 isoforms.
Bozatzi P et al.
Biochemical Society Transactions, 2018
Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair.
Maruthappu T et al.
The Journal of Investigative Dermatology, 2018
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