GGCX Chromosome 2

Gamma-glutamyl carboxylase
60 variants 60 Health Risk

Upload your DNA to see your personal genotypes for variants in GGCX.

What This Gene Does
This gene encodes an integral membrane protein of the rough endoplasmic reticulum that carboxylates glutamate residues of vitamin K-dependent proteins to gamma carboxyl glutamate, a modification that is required for their activity. The vitamin K-dependent protein substrates have a propeptide that binds the enzyme, with carbon dioxide, dioxide, and reduced vitamin K acting as co-substrates. Vitamin K-dependent proteins affect a number of physiologic processes including blood coagulation, prevention of vascular calcification, and inflammation. Allelic variants of this gene have been associated with pseudoxanthoma elasticum-like disorder with associated multiple coagulation factor deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015]
Associated Conditions (14)
Inborn genetic diseases
Vitamin K-dependent clotting factors
combined deficiency of
type 1
GGCX-related disorder
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Uterine corpus endometrial carcinoma
Sarcoma
Cervical cancer
Thymoma
Nonpapillary renal cell carcinoma
Ovarian serous cystadenocarcinoma
Malignant tumor of esophagus
GGCX - Related Disorders
Key Variants
RS113962887
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1262224787
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS1284965933
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS141040739
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS145056129
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS146085955
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS146930374
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS147427088
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS149039591
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS149603998
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS1691972995
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
RS371622780
Conflicting classifications of pathogenicity
Vitamin K-dependent clotting factors, combined deficiency of, type 1
Health Risk
All Variants (60)
RSID Category Clinical Significance Conditions
RS564812596 Health Risk Pathogenic GGCX-related disorder, GGCX-related disorder
RS575528363 Health Risk Pathogenic Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency, Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
RS750767043 Health Risk Pathogenic GGCX - Related Disorders, GGCX - Related Disorders
RS755908721 Health Risk Pathogenic
RS786205096 Health Risk Pathogenic Vitamin K-dependent clotting factors, combined deficiency of, type 1
RS121909683 Health Risk Pathogenic/Likely pathogenic Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency, Vitamin K-dependent clotting factors, combined deficiency of
RS1558806955 Health Risk Pathogenic/Likely pathogenic GGCX-related disorder, GGCX-related disorder
RS748892794 Health Risk Pathogenic/Likely pathogenic GGCX-related disorder, GGCX-related disorder
RS753122975 Health Risk Pathogenic/Likely pathogenic Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency, Vitamin K-dependent clotting factors, combined deficiency of
RS779018917 Health Risk Pathogenic/Likely pathogenic Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency, Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
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