Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10001 to 10010 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10001
Phosphatidylinositol specific phospholipase C X domain containing 2
PLCXD-2
Atrial fibrillation, Atrial flutter, Crohn disease, Hemorrhoid, Ileocolitis, Oligodendroglioma

10002
Phosphatidylinositol specific phospholipase C X domain containing 3
-
Alzheimer disease, Bipolar disorder, Breast cancer

10003
Phospholipase C zeta 1
Czeta, NYD-SP27, PLC-zeta-1, PLCzeta, SPGF17
Spermatogenic failure

10004
Phospholipase D1
CVDD, CVDP1
Cardiac valvular dysplasia, Cardiomegaly, Cataract, Coronary stenosis, Duodenal ulcer, Major depressive disorder, Tetralogy of fallot

10005
Phospholipase D2
PLD1C
Alzheimer disease, Cardiomegaly, Systemic lupus erythematosus

10006
Phospholipase D family member 3
AD19, HU-K4, HUK4, SCA46
Alzheimer disease, Charcot-marie-tooth disease, Hereditary motor and sensory neuropathies, Spinocerebellar ataxia

10007
Phospholipase D family member 4
C14orf175
Rheumatoid arthritis, Central nervous system cancer, Glioblastoma, Glioma, Liver cirrhosis, Systemic lupus erythematosus

10008
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

10009
Phospholipase D family member 6
ZUC
Male infertility

10010
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
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