Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "P"
1001 to 1010 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1001
Peroxiredoxin 4
AOE37-2, AOE372, HEL-S-97n, PRX-4
Allergic contact dermatitis, Hyperglycemia, Diffuse large b-cell lymphoma

1002
Peroxiredoxin 5
ACR1, AOEB166, B166, HEL-S-55, PLP, PMP20, PRDX6, PRXV, SBBI10, prx-V
Attention deficit hyperactivity disorder, Basal cell carcinoma, Crohn disease, Hypothyroidism, Iga nephropathy, Inflammatory bowel disease, Multiple sclerosis, Non-melanoma skin carcinoma, Biliary cholangitis, Psoriasis, Psoriasis vulgaris, Rheumatoid arthritis, Sarcoidosis, Skin cancer, Skin neoplasms
View all (4 more)

1003
Peroxiredoxin 6
1-Cys, AOP2, HEL-S-128m, LPCAT-5, NSGPx, PRX, aiPLA2, p29
Hepatocellular carcinoma, Contact dermatitis, Down syndrome, Lung neoplasms, Myocardial ischemia, Schizophrenia

1004
PRELI domain containing 1
CGI-106, PRELI, PX19, SBBI12
Gout

1005
PRELI domain containing 2
-
Alzheimer disease, Dyshidrosis, Rheumatic fever

1006
PRELI domain containing 3A
C18orf43, HFL-EDDG1, SLMO1
Uveal melanoma

1007
PRELI domain containing 3B
C20orf45, SLMO2, UPS2, dJ543J19.5
Coronary artery disease, Hypertension, Diabetes mellitus type 2

1008
Proline and arginine rich end leucine rich repeat protein
MST161, MSTP161, SLRR2A
Obesity

1009
Prolyl endopeptidase
PE, PEP
Amnesia, Androgenetic alopecia, Asthma, Colorectal cancer, Duchenne muscular dystrophy, Glomerulonephritis, Retrograde amnesia, Stomach neoplasms

1010
Prolyl endopeptidase like
CMS22
Hypotonia-cystinuria syndrome, Congenital myasthenic syndrome, Cystine urolithiasis, Cystinuria, Intellectual developmental disorder, Myasthenic syndrome