ANKRD13C

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Description

The ANKRD13C (ankyrin repeat domain 13C) is a protein-coding gene located on chromosome 1.

ANKRD13C, short for Ankyrin repeat domain-containing protein 13C, is a protein produced in humans by the ANKRD13C gene. It is predicted to interact with TMEM255A (Transmembrane Protein Domain 255A). You can find more information about ANKRD13C and its location on the human genome through the UCSC Genome Browser.

ANKRD13C acts as a molecular chaperone for G protein-coupled receptors, regulating their production and movement from the endoplasmic reticulum.

ANKRD13C is also known as dJ677H15.3.

Associated Diseases

• colorectal cancer
• hemoglobin D disease
• hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
• dominant beta-thalassemia
• hemoglobin H disease
• hemoglobin E disease
• retinitis pigmentosa and erythrocytic microcytosis
• hemoglobin C-beta-thalassemia syndrome
• delta-beta-thalassemia
• alpha-thalassemia-myelodysplastic syndrome
• hemoglobin E-beta-thalassemia syndrome
• dehydrated hereditary stomatocytosis
• X-linked retinoschisis
• cyanosis, transient neonatal
• beta-thalassemia-X-linked thrombocytopenia syndrome
• hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
• X-linked retinal dysplasia