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
10241 to 10250 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

10241
Periphilin 1
CR, HSPC206, HSPC232
Central nervous system cancer, Colorectal cancer, Coronary artery disease, Glioblastoma, Glioma, Gout

10242
Peptidylprolyl isomerase A
CYPA, CYPH, HEL-S-69p
Non-small-cell lung carcinoma, Squamous cell carcinoma, Clonal hematopoiesis, Mouth neoplasms, Schizophrenia, Stomach neoplasms

10243
Peptidylprolyl isomerase A like 4F
-
Alzheimer disease

10244
Peptidylprolyl isomerase A pseudogene 59
-
Alzheimer disease, Atrophic gastritis, Obesity

10245
Peptidylprolyl isomerase B
CYP-S1, CYPB, HEL-S-39, OI9, SCYLP
Bone fragility with contractures, arterial rupture, and deafness, Desbuquois syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

10246
Peptidylprolyl isomerase C
CYPC
Stomach neoplasms

10247
Peptidylprolyl isomerase D
CYP-40, CYPD
Alzheimer disease, Bipolar disorder, Insomnia, Schizophrenia

10248
Peptidylprolyl isomerase F
CYP3, CyP-M, Cyp-D, CypD
Intestinal disease, Selective iga deficiency disease, Diabetes mellitus type 2

10249
Peptidylprolyl isomerase G
CARS-Cyp, CYP, SCAF10, SRCyp
Alzheimer disease

10250
Peptidylprolyl isomerase like 1
CGI-124, CYPL1, PCH14, PPIase, hCyPX
Congenital pontocerebellar hypoplasia, Major depressive disorder, Neurodevelopmental disorder, Pontocerebellar hypoplasia, Scoliosis