|
1801
|
|
|
Calcium activated nucleotidase 1 |
DBQD, DBQD1, EDM7, SCAN-1, SCAN1, SHAPY |
Arthritis, Brachydactyly, Camptodactyly of fingers, Congenital clubfoot, Congenital genu recurvatum, Desbuquois dysplasia, Desbuquois syndrome, Dwarfism, Epiphyseal dysplasia, Glaucoma, Glaucoma, congenital, Hypotrichosis, Mental retardation, Microstomia, Motor delay, Multiple congenital anomalies, Myopia, Obesity, Osteoporosis, Proptosis, Radioulnar synostosis, Scoliosis, Ventricular septal defectView all (8 more) |
|
1802
|
|
|
USH1 protein network component sans |
ANKS4A, SANS |
Anxiety disorder, Cataract, Cerebral cortical atrophy, Ciliopathies, Congenital sensorineural hearing loss, Developmental delay, Disorder of eye, Hallucinations, Hearing loss, Hemianopsia, Hereditary retinal dystrophy, Mental depression, Mental retardation, Nonsyndromic deafness, Nyctalopia, Rod-cone dystrophy, Schizophrenia, Subcortical cerebral atrophy, Usher syndromeView all (4 more) |
|
1803
|
|
|
Zona pellucida binding protein 2 |
ZPBPL |
Allergic rhinitis, Ankylosing spondylitis, Asthma, Atrial fibrillation, Cholangitis, Crohn disease, Paroxysmal atrial fibrillation, Biliary cirrhosis, Psoriasis, Rheumatoid arthritis, Ulcerative colitis |
|
1804
|
|
|
OVCA2 serine hydrolase domain containing |
- |
|
|
1805
|
|
|
Spermatogenesis associated 32 |
AEP2, C17orf46, TEX34, VAD1.2 |
|
|
1806
|
|
|
Cyclin N-terminal domain containing 1 |
CNTD, COSA1 |
|
|
1807
|
|
|
Transmembrane protein 132E |
DFNB99 |
|
|
1808
|
|
|
Beta-1,4-N-acetyl-galactosaminyltransferase 2 (SID blood group) |
B4GALT, GALGT2 |
|
|
1809
|
|
|
Seizure related 6 homolog |
BSRPC |
|
|
1810
|
|
|
Ankyrin repeat domain 13B |
- |
|
