FCRL2
Description
The FCRL2 (Fc receptor like 2) is a protein-coding gene located on chromosome 1.
Fc receptor-like protein 2 is a protein that in humans is encoded by the FCRL2 gene.
FCRL2 may play a regulatory role in both normal and cancerous B cell development.
FCRL2 is also known as CD307b, FCRH2, IFGP4, IRTA4, SPAP1, SPAP1A, SPAP1B, SPAP1C.
Associated Diseases
- multiple sclerosis
- lysosomal storage disease
- Alzheimer disease
- Parkinson disease
- systemic lupus erythematosus
- isolated asymptomatic elevation of creatine phosphokinase
- plasma fibronectin deficiency
- pentosuria
- hypoparathyroidism, familial isolated, 2
- myopathy due to calsequestrin and SERCA1 protein overload
- pseudohypoparathyroidism type 2
- metabolic myopathy due to lactate transporter defect
