Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9991 to 10000 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9991
Pleckstrin homology and RUN domain containing M1
AP162, B2, OPTA3, OPTB6
Alzheimer disease, Androgenetic alopecia, Osteopetrosis, Breast cancer, Desbuquois syndrome, Ovarian epithelial cancer, Neurotic disorder, Ovarian cancer, Ovarian serous carcinoma, Parkinson disease, Post-traumatic stress disorder, Systemic lupus erythematosus

9992
Pleckstrin homology and RUN domain containing M2
SKIP
Dilated cardiomyopathy, Coronary artery disease, Insomnia, Left ventricular disease, Diabetes mellitus type 2

9993
Pleckstrin homology domain containing M3
DAPR, PLEKHM1L
Endometriosis, Diabetes mellitus type 2, Uterine fibroid

9994
Pleckstrin homology domain containing O1
CKIP-1, CKIP1, JBP, OC120
Bipolar disorder, Bipolar depression, Schizophrenia

9995
Pleckstrin homology domain containing O2
PLEKHQ1, PP1628, pp9099
Internal carotid artery stenosis

9996
Pleckstrin homology domain containing S1
C10orf81, HEL185
Colorectal cancer, Obesity, Open angle glaucoma, Upper aerodigestive tract neoplasm

9997
Plasminogen
HAE4
Angioedema, Hemolytic uremic syndrome, Cardiovascular disease, Central nervous system cancer, Kidney disease, Conjunctivitis, Coronary artery disease, Cystic fibrosis, Deep vein thrombosis, Dementia, Diabetic neuropathy, Glioblastoma, Glioma, Heart disease, Hypertension
View all (20 more)

9998
Plasminogen receptor with a C-terminal lysine
AD025, C9orf46, MDS030, PLG-RKT, Plg-R(KT)
Autoimmune thyroid disease, Hypothyroidism, Obesity, Polycystic ovary syndrome, Rheumatoid arthritis, Diabetes mellitus type 1

9999
Perilipin 1
FPLD4, PERI, PLIN
Color vision deficiency, Partial lipodystrophy, Lipodystrophy, Obesity

10000
Perilipin 2
ADFP, ADRP
Fatty liver, Fatty liver, alcoholic, Stomach neoplasms