Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
10511 to 10520 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10511
Serine protease 55
CT153, T-SP1, TSP1, UNQ9391
Barrett esophagus, Esophageal adenocarcinoma, Neurotic disorder, Obesity, Psychiatric disorders

10512
Serine protease 56
MCOP6
Angle closure glaucoma, Congenital cystic eyeball, Eye disease, Glaucoma, Hyperopia, Microphthalmia, Microphthalmos, Myopia, Nanophthalmos

10513
Serine protease 8
CAP1, PROSTASIN
Cardiovascular disease, Dermatologic disorder, Disorder of pregnancy, Neural tube defect, Neural tube defects, x-linked, Prostatic neoplasms, Skin disease

10514
Phosphoribosyl transferase domain containing 1
HHGP
Asthma, Squamous cell carcinoma, Corneal edema, Coronary artery disease, Duodenal ulcer, Hypertension, Insomnia, Liver cirrhosis, Mouth neoplasms, Obesity, Open angle glaucoma, Ovarian neoplasms, Post-traumatic stress disorder

10515
Protogenin
IGDCC5
Cataract, Liver cirrhosis, Prostate cancer, Testicular carcinoma, Testicular germ cell tumor

10516
Proteinase 3
ACPA, AGP7, C-ANCA, CANCA, MBN, MBT, NP-4, NP4, P29, PR-3, PR3
Anti-neutrophil antibody associated vasculitis, Granulomatosis with polyangiitis, Iga nephropathy

10517
Prune exopolyphosphatase 1
DRES-17, DRES17, H-PRUNE, HTCD37, NMIHBA, PRUNE
Gestational diabetes, Neurodevelopmental disorder, Diabetes mellitus type 2

10518
Prune homolog 2 with BCH domain
BMCC1, BNIPXL, C9orf65, KIAA0367
Central nervous system cancer, Cervical cancer, Dental caries, Glioblastoma, Glioma, Liver cirrhosis, Skin disease, Upper aerodigestive tract neoplasm

10519
Periaxin
CMT4F
Charcot-marie-tooth disease, Congenital cataract, Dejerine-sottas disease, Distal spinal muscular atrophy, Gaucher disease, Hereditary motor and sensory neuropathies, Hereditary sensory and motor neuropathy, Hypertrophic neuropathy, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Spinocerebellar ataxia

10520
Peroxiredoxin like 2A
Adrx, C10orf58, FAM213A, PAMM
Atrial fibrillation, Cataract, Gout, Heart failure, Hypertension, Peptic ulcer disease, Sarcoidosis