|
291
|
|
|
Peptidyl arginine deiminase 6 |
OZEMA16, PREMBL2, hPADVI |
|
|
292
|
|
|
Pancreatic and duodenal homeobox 1 |
GSF, IDX-1, IPF1, IUF1, MODY4, PAGEN1, PDX-1, STF-1 |
Apraxia, Arthrogryposis multiplex congenita, Clinodactyly, Congenital heart defects, Hyperinsulinemic hypoglycemia, Pancreatic hypoplasia, Developmental delay, Diabetes mellitus, Exocrine pancreatic insufficiency, Hepatocellular adenoma, Hyperglycemia, Hypoinsulinemia, Mental retardation, Ketonuria, Ketosis, Kidney disease, Mason type diabetes, Monogenic diabetes, Motor delay, Myoclonic seizures, Hypoglycemia, Nervous system diseases, Obesity, Congenital pancreatic agenesis, Pancreatic neoplasm, Pancreatic cancer, Peripheral axonal neuropathy, Ptosis, Renal cyst, Renal tubular disorder, Retinal diseases, SeizureView all (17 more) |
|
293
|
|
|
Protein tyrosine phosphatase receptor type Q |
DFNA73, DFNB84, DFNB84A, PTPGMC1, R-PTP-Q |
|
|
294
|
|
|
Patatin like domain 7, lysophospholipase |
C9orf111, NTE-R1, NTEL1 |
|
|
295
|
|
|
PSMA3 antisense RNA 1 |
- |
|
|
296
|
|
|
Photoreceptor cilium actin regulator |
C2orf71, RP54 |
Cataract, Ciliopathies, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Macular dystrophy, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (4 more) |
|
297
|
|
|
Proteasome assembly chaperone 4 |
C6orf86, PAC4, Pba4, bA506K6.2 |
|
|
298
|
|
|
Peptidyl-tRNA hydrolase domain containing 1 |
C2orf79, NEDPBA |
|
|
299
|
|
|
Pecanex 3 |
PCNXL3 |
|
|
300
|
|
|
Pleckstrin homology and coiled-coil domain containing D1 |
UPF0639 |
|
