Homo sapiens crystallin gamma C variant (CRYGC) mRNA, complete cds

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The Y46D Mutation Destabilizes Dense Packing of the Second Greek Key Pair of Human γC-Crystallin Causing Congenital Nuclear Cataracts. [Biochemistry. 2023]
The Y46D Mutation Destabilizes Dense Packing of the Second Greek Key Pair of Human γC-Crystallin Causing Congenital Nuclear Cataracts.
Vendra VPR, Ostrowski C, Clark R, Dyba M, Tarasov SG, Hejtmancik JF. Biochemistry. 2023 Jun 20; 62(12):1864-1877. Epub 2023 May 15.
Case Report: A de novo Variant of CRYGC Gene Associated With Congenital Cataract and Microphthalmia. [Front Genet. 2022]
Case Report: A de novo Variant of CRYGC Gene Associated With Congenital Cataract and Microphthalmia.
Peng Y, Zheng Y, Deng Z, Zhang S, Tan Y, Hu Z, Tao L, Luo Y. Front Genet. 2022; 13:866246. Epub 2022 May 27.
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.

Homo sapiens
Homo sapiens
Genomic characterization of ovarian cancer spheroids

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Nucleotide