Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10681 to 10690 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10681
PTTG1 regulator of sister chromatid separation, securin
EAP1, ECRAR, HPTTG, PTTG, TUTR1
Hepatocellular carcinoma, Psoriasis, Scoliosis, Sjogren syndrome

10682
PTTG1 interacting protein
C21orf1, C21orf3, PBF, PTTG1IP1
Ankylosing spondylitis, Cholecystolithiasis, Gallstones

10683
PTTG1IP family member 2
-
Retinopathy of prematurity

10684
Pentraxin 3
TNFAIP5, TSG-14
Cystic fibrosis, Depression, Dermatologic disorder, Major depressive disorder, Pulmonary fibrosis, Skin disease

10685
Pentraxin 4
C16orf38
Hemolytic anemia, Otosclerosis, Rheumatoid arthritis

10686
Pseudouridine 5'-phosphatase
DXF68S1E, FAM16AX, GS1, HDHD1, HDHD1A
Scoliosis

10687
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

10688
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

10689
Pumilio RNA binding family member 2
PUMH2, PUML2
Autism, Iron metabolism disorder, Metabolic syndrome, Osteoarthritis

10690
Pumilio RNA binding family member 3
HA-8, HLA-HA8, KIAA0020, PEN, PUF-A, PUF6, XTP5
Alzheimer disease, Obesity