Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10321 to 10330 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10321
PRELI domain containing 2
-
Alzheimer disease, Dyshidrosis

10322
PRELI domain containing 3A
C18orf43, HFL-EDDG1, SLMO1
Uveal melanoma

10323
PRELI domain containing 3B
C20orf45, SLMO2, UPS2, dJ543J19.5
Coronary artery disease, Hypertension, Diabetes mellitus type 2

10324
Proline and arginine rich end leucine rich repeat protein
MST161, MSTP161, SLRR2A
Obesity

10325
Prolyl endopeptidase
PE, PEP
Amnesia, Androgenetic alopecia, Asthma, Colorectal cancer, Duchenne muscular dystrophy, Glomerulonephritis, Retrograde amnesia, Stomach neoplasms

10326
Prolyl endopeptidase like
CMS22
Hypotonia-cystinuria syndrome, Congenital myasthenic syndrome, Cystine urolithiasis, Cystinuria, Intellectual developmental disorder, Myasthenic syndrome

10327
Phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 1
P-REX1
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Breast cancer, Cancer, Cardiovascular disease, Central serous retinopathy, Colorectal cancer, Colonic neoplasms, Colorectal adenoma, Coronary artery disease, Estrogen-receptor negative breast cancer, Hypertension, Hypothyroidism, Lung cancer
View all (16 more)

10328
Phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2
DEP.2, DEPDC2, P-REX2, PPP1R129
Cerebral arteriovenous malformations, Bladder exstrophy, Dry eye syndrome, Pancreatic cancer

10329
Perforin 1
HPLH2, P1, PFP
Aplastic anemia, Autism, Autoinflammatory syndrome, Crohn disease, Hemophagocytic lymphohistiocytosis, Hereditary hemophagocytic lymphohistiocytosis, Multiple sclerosis, Nonalcoholic fatty liver disease

10330
Proteoglycan 2, pro eosinophil major basic protein
BMPG, MBP, MBP1, proMBP
Alzheimer disease, Autism