Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
1321 to 1330 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1321
PTTG1IP family member 2
-
Retinopathy of prematurity

1322
Pentraxin 3
TNFAIP5, TSG-14
Cystic fibrosis, Depression, Dermatologic disorder, Major depressive disorder, Pulmonary fibrosis, Skin disease

1323
Pentraxin 4
C16orf38
Hemolytic anemia, Otosclerosis, Rheumatoid arthritis

1324
Pseudouridine 5'-phosphatase
DXF68S1E, FAM16AX, GS1, HDHD1, HDHD1A
Scoliosis

1325
Poly(U) binding splicing factor 60
FIR, RoBPI, SIAHBP1, VRJS
8q24.3 microdeletion syndrome, Charge syndrome, Desbuquois syndrome, Intellectual developmental disorder dysmorphic cardiac short stature, Mesothelioma, Necrosis, Neurodevelopmental disorder, Verheij syndrome

1326
Pumilio RNA binding family member 1
HSPUM, NEDMSF, PUMH, PUMH1, PUML1, SCA47
Colorectal cancer, Gout, Intellectual developmental disorder, Metabolic syndrome, Neurodevelopmental disorder, Spastic ataxia, Spinocerebellar ataxia, Hypertension, Diabetes mellitus, type 2

1327
Pumilio RNA binding family member 2
PUMH2, PUML2
Autism, Iron metabolism disorder, Metabolic syndrome, Osteoarthritis

1328
Pumilio RNA binding family member 3
HA-8, HLA-HA8, KIAA0020, PEN, PUF-A, PUF6, XTP5
Alzheimer disease, Obesity

1329
Purine rich element binding protein A
MRD31, NEDRIHF, PUR-ALPHA, PUR1, PURALPHA
Neurodevelopmental disorder, Congenital neurologic anomalies, Epilepsy, Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability

1330
Purine rich element binding protein B
PURBETA
Bipolar disorder, Clonal hematopoiesis, Major depressive disorder, Schizoaffective disorder, Squamous cell carcinoma