Homo sapiens KIAA1785 mRNA for KIAA1785 protein

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A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia. [Hum Mol Genet. 2023]
A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia.
Dubey AA, Krygier M, Szulc NA, Rutkowska K, Kosińska J, Pollak A, Rydzanicz M, Kmieć T, Mazurkiewicz-Bełdzińska M, Pokrzywa W, et al. Hum Mol Genet. 2023 Mar 20; 32(7):1152-1161.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
Molecular basis for ubiquitin ligase CRL2(FEM1C)-mediated recognition of C-degron. [Nat Chem Biol. 2021]
Molecular basis for ubiquitin ligase CRL2(FEM1C)-mediated recognition of C-degron.
Yan X, Wang X, Li Y, Zhou M, Li Y, Song L, Mi W, Min J, Dong C. Nat Chem Biol. 2021 Mar; 17(3):263-271. Epub 2021 Jan 4.

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Nucleotide