ZCCHC17

• SHARE NOW |
• Tweet Opens in a new window.
• Pin it Opens in a new window.
• Share Opens in a new window.
• Share Opens in a new window.
• Email Opens in a new window.

---

Description

The ZCCHC17 (zinc finger CCHC-type containing 17) is a protein-coding gene located on chromosome 1.

Nucleolar protein of 40 kDa is a protein that in humans is encoded by the ZCCHC17 gene.

ZCCHC17 is also known as HSPC251, PS1D, pNO40.

Associated Diseases

• beta-thalassemia-X-linked thrombocytopenia syndrome
• thrombocytopenia 4
• dominant beta-thalassemia
• macrothrombocytopenia, isolated, 2, autosomal dominant
• hemoglobin C-beta-thalassemia syndrome
• hemoglobin H disease
• platelet-type bleeding disorder 15
• erythroleukemia, familial, susceptibility to
• hemoglobin D disease
• bleeding disorder, platelet-type, 24
• thrombocytopenia 2
• hemolytic anemia due to diphosphoglycerate mutase deficiency
• platelet-type bleeding disorder 10
• autosomal dominant macrothrombocytopenia
• thrombocytopenia, anemia, and myelofibrosis