C1QL2
Description
The C1QL2 (complement C1q like 2) is a protein-coding gene located on chromosome 2.
C1QL2 may play a role in regulating the formation of excitatory synapses on hippocampal neurons, but it does not appear to influence inhibitory synapses.
C1QL2 is also known as C1QTNF10, CTRP10.
Associated Diseases
- female infertility due to oocyte meiotic arrest
- premature ovarian failure 19
- oocyte maturation defect 9
- hepatorenocardiac degenerative fibrosis
- congenital hydronephrosis
- nephronophthisis
- focal segmental glomerulosclerosis 7
- nephronophthisis 3
- familial juvenile hyperuricemic nephropathy type 2
- renal dysplasia
- congenital anomalies of kidney and urinary tract 1
