CEACAM7

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Description

The CEACAM7 (CEA cell adhesion molecule 7) is a protein-coding gene located on chromosome 19.

Carcinoembryonic antigen-related cell adhesion molecule 7 is a protein that in humans is encoded by the CEACAM7 gene. References: External links: Human CEACAM7 genome location and CEACAM7 gene details page in the UCSC Genome Browser.

CEACAM7 is also known as CGM2.

Associated Diseases

• ringed hair disease
• Griscelli syndrome type 3
• uncombable hair syndrome
• hyperinsulinism due to INSR deficiency
• hypertriglyceridemia 2
• Gorham-Stout disease
• cholesterol-ester transfer protein deficiency
• hyperinsulinism due to glucokinase deficiency
• microcephaly-albinism-digital anomalies syndrome
• hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
• pili bifurcati
• beta-thalassemia-X-linked thrombocytopenia syndrome
• alpha-thalassemia-myelodysplastic syndrome
• exercise-induced hyperinsulinism
• alpha thalassemia-intellectual disability syndrome type 1