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
10321 to 10330 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10321
Protein phosphatase 4 regulatory subunit 3B
FLFL2, PP4R3B, PSY2, SMEK2, smk1
Metabolic syndrome, Diabetes mellitus type 2, Vitiligo

10322
Protein phosphatase 4 regulatory subunit 3C
FLFL3P, PPP4R3CP, SMEK3P, smk1
Hepatocellular carcinoma

10323
Protein phosphatase 4 regulatory subunit 4
CFAP14, KIAA1622, PP4R4
Obstructive pulmonary disease, Oligodendroglioma

10324
Protein phosphatase 5 catalytic subunit
PP5, PPP5, PPT
Ankylosing spondylitis, Atrial fibrillation, Crohn disease, Inflammatory bowel disease, Neurotic disorder, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

10325
Protein phosphatase 6 catalytic subunit
PP6, PP6C
Cannabis abuse, Basal cell carcinoma, Melanoma, Substance abuse

10326
Protein phosphatase 6 regulatory subunit 1
KIAA1115, PP6R1, SAP190, SAPS1
Cutaneous leishmaniasis

10327
Protein phosphatase 6 regulatory subunit 2
KIAA0685, PP6R2, SAP190, SAPS2
Alzheimer disease, Charcot-marie-tooth disease, Color vision deficiency, Parkinson disease

10328
Protein phosphatase 6 regulatory subunit 3
C11orf23, PP6R3, SAP190, SAPL, SAPLa, SAPS3
Bone disease, Osteoporosis

10329
PPARG related coactivator 1
PRC
Breast cancer, Willis-ekbom disease

10330
Palmitoyl-protein thioesterase 1
CLN1, INCL, PPT
Neuronal ceroid lipofuscinosis, Congenital neurologic anomalies, Intellectual developmental disorder, Neurodevelopmental disorder, Retinitis pigmentosa, Spastic ataxia, Visual disorder