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"
641 to 650 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

641
Phospholipase D1
CVDD, CVDP1
Cardiac valvular dysplasia, Cardiomegaly, Cataract, Coronary stenosis, Duodenal ulcer, Major depressive disorder, Tetralogy of fallot

642
Phospholipase D2
PLD1C
Alzheimer disease, Cardiomegaly, Systemic lupus erythematosus

643
Phospholipase D family member 3
AD19, HU-K4, HUK4, SCA46
Alzheimer disease, Charcot-marie-tooth disease, Hereditary motor and sensory neuropathies, Spinocerebellar ataxia

644
Phospholipase D family member 4
C14orf175
Rheumatoid arthritis, Central nervous system cancer, Glioblastoma, Glioma, Systemic lupus erythematosus

645
Phospholipase D family member 5
PLDC
Astrocytoma, Autism, Central nervous system cancer, Color vision deficiency, Dementia, Dental caries, Glioblastoma, Glioma, Myositis, Oligodendroglioma, Squamous cell carcinoma, Hypertension

646
Phospholipase D family member 6
ZUC
Male infertility

647
Plectin
EBS1, EBS5A, EBS5B, EBS5C, EBS5D, EBSMD, EBSND, EBSO, EBSOG, EBSPA, HD1, LGMD2Q, LGMDR17, PCN, PLEC1, PLEC1b, PLTN
Alzheimer disease, Aplasia cutis congenita, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Limb girdle muscular dystrophy, Bipolar disorder, Dilated cardiomyopathy, Cholelithiasis, Congenital myasthenic syndrome, Epidermolysa bullosa simplex and limb girdle muscular dystrophy, Epidermolysis bullosa, Junctional epidermolysis bullosa, Hemorrhoid, Limb-girdle muscular dystrophy, Multiple sclerosis
View all (6 more)

648
Pleckstrin
P47, PLEK1
Rheumatoid arthritis, Celiac disease, Follicular lymphoma, Multiple sclerosis, Obesity, Oligodendroglioma, Osteoporosis, Venous thromboembolism

649
Pleckstrin 2
-
Major depressive disorder, Prostatic neoplasms

650
Pleckstrin homology domain containing A1
TAPP1
Alzheimer disease, Attention deficit hyperactivity disorder, Autoimmune disease, Autoimmune thyroid disease, Color vision deficiency, Diabetes mellitus type 2, Diverticular disease, Glaucoma, Hypothyroidism, Schizophrenia, Stroke, Diabetes mellitus type 1