CAB39L

---

Description

The CAB39L (calcium binding protein 39 like) is a protein-coding gene located on chromosome 13.

Calcium-binding protein 39-like is a protein encoded by the CAB39L gene in humans. Information about its location and gene details can be found on the UCSC Genome Browser.

CAB39L is part of a complex that binds and activates STK11/LKB1. Within this complex, CAB39L is crucial for stabilizing the interaction between CAB39/MO25 (either CAB39/MO25alpha or CAB39L/MO25beta) and STK11/LKB1.

CAB39L is also known as MLAA-34, MO25-BETA, MO2L, bA103J18.3.

Associated Diseases

• Parkinson disease
• endometrial cancer
• dominant beta-thalassemia
• hemoglobin D disease
• hemoglobin C-beta-thalassemia syndrome
• alpha thalassemia-intellectual disability syndrome type 1
• hemoglobin H disease
• Heinz body anemia
• hemolytic anemia due to diphosphoglycerate mutase deficiency
• delta-beta-thalassemia