unknown [Homo sapiens]

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[Partial research progress of GGCX pathogenic variation associated phenotypes]. [Zhonghua Yi Xue Yi Chuan Xue Z...]
[Partial research progress of GGCX pathogenic variation associated phenotypes].
Shen G, Liu H, Shen Y, Xi S. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jun 10; 39(6):646-650.
GGCX variants leading to biallelic deficiency to γ-carboxylate GRP cause skin laxity in VKCFD1 patients. [Hum Mutat. 2022]
GGCX variants leading to biallelic deficiency to γ-carboxylate GRP cause skin laxity in VKCFD1 patients.
Ghosh S, Kraus K, Biswas A, Müller J, Forin F, Singer H, Höning K, Hornung V, Watzka M, Oldenburg J, et al. Hum Mutat. 2022 Jan; 43(1):42-55. Epub 2021 Dec 2.
γ-Glutamyl carboxylase mutations differentially affect the biological function of vitamin K-dependent proteins. [Blood. 2021]
γ-Glutamyl carboxylase mutations differentially affect the biological function of vitamin K-dependent proteins.
Hao Z, Jin DY, Chen X, Schurgers LJ, Stafford DW, Tie JK. Blood. 2021 Jan 28; 137(4):533-543.

RefSeq genomic sequence
See the genomic reference sequence for the GGCX gene (NG_011811.2).
RefSeq protein isoforms
See 11 reference sequence protein isoforms for the GGCX gene.

Nucleotide
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BioSystems
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein