Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10251 to 10260 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10251
Peptidylprolyl isomerase like 2
CYC4, CYP60, Cyp-60, UBOX7, hCyP-60
Alzheimer disease, Autism, Dementia, Diabetes mellitus type 1

10252
Peptidylprolyl isomerase like 3
CYPJ
Basal cell carcinoma, Breast cancer, Estrogen-receptor negative breast cancer, Iga nephropathy

10253
Peptidylprolyl isomerase like 4
HDCME13P
Central nervous system cancer, Glioblastoma, Glioma, Rheumatoid arthritis

10254
Peptidylprolyl isomerase like 6
PPIase, RSPH12, bA425D10.6, dJ919F19.1
Alzheimer disease, Astrocytoma, Lung cancer, Squamous cell carcinoma

10255
Diphosphoinositol pentakisphosphate kinase 2
CFAP160, DFNB100, HISPPD1, IP7K2, VIP2
Isolated sensorineural deafness, Deafness, Diabetes mellitus, Diabetic eye disease, Hearing loss, Insomnia, Diabetes mellitus type 2

10256
Periplakin
-
Lung cancer, Prostate cancer, Prostatic neoplasms, Seborrheic keratosis

10257
Protein phosphatase, Mg2+/Mn2+ dependent 1A
PP2C-ALPHA, PP2CA, PP2Calpha
Coronary artery disease, Seasonal allergic rhinitis

10258
Protein phosphatase, Mg2+/Mn2+ dependent 1B
PP2C-beta, PP2C-beta-X, PP2CB, PP2CBETA, PPC2BETAX
Cholecystolithiasis, Myocardial ischemia

10259
Protein phosphatase, Mg2+/Mn2+ dependent 1D
IDDGIP, JDVS, PP2C-DELTA, WIP1
Nonsyndromic intellectual disability, Brain stem neoplasms, Breast cancer, Breast neoplasms, Desbuquois syndrome, Glioma, Gout, Intellectual developmental disorder growth other organ, Neurodevelopmental disorder

10260
Protein phosphatase, Mg2+/Mn2+ dependent 1E
CAMKPN, CaMKP-N, POPX1, PP2CH, caMKN
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Color vision deficiency, Colorectal neoplasms, Mulibrey nanism, Schizophrenia, Diabetes mellitus type 2