Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9571 to 9580 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9571
Protocadherin gamma subfamily C, 4
NEDGS, PCDH-GAMMA-C4
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

9572
PC-esterase domain containing 1B
FAM113B
Alzheimer disease, Color vision deficiency, Colorectal cancer, Lung cancer, Prostate cancer, Skin disease, Squamous cell carcinoma, Diabetes mellitus type 2

9573
PCF11 cleavage and polyadenylation factor subunit
-
Obesity

9574
Polycomb group ring finger 2
MEL-18, RNF110, TPFS, ZNF144
Global developmental delay, Intellectual developmental disorder, Turnpenny-fry syndrome, Wolfram syndrome

9575
Polycomb group ring finger 3
DONG1, RNF3, RNF3A
Astrocytoma, Attention deficit hyperactivity disorder, Autism, Parkinson disease, Schizophrenia, Diabetes mellitus type 2

9576
Polycomb group ring finger 6
MBLR, RNF134
Anorexia nervosa, Attention deficit hyperactivity disorder, Dyslexia, Insomnia, Schizophrenia, Substance abuse, Uterine fibroid

9577
PCI domain containing 2
F10
Atrial fibrillation, Thrombocytopenia

9578
Phosphorylated CTD interacting factor 1
C20orf67, CAPAM, MT-A70, PPP1R121, hCAPAM, hPCIF1
Metabolic syndrome, Diabetes mellitus type 2

9579
Phosphoenolpyruvate carboxykinase 1
PCKDC, PEPCK-C, PEPCK1, PEPCKC
Alzheimer disease, Hepatocellular carcinoma, Celiac disease, Color vision deficiency, Congestive heart failure, Experimental diabetes, Diabetes mellitus type 2, Heart failure, Liver cirrhosis, Metabolic syndrome, Obesity, Schizophrenia

9580
Phosphoenolpyruvate carboxykinase 2, mitochondrial
PEPCK, PEPCK-M, PEPCK2, mtPCK2
Hypoxia, Liver cirrhosis, Retinitis pigmentosa