Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10631 to 10640 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10631
Peptidyl-tRNA hydrolase domain containing 1
C2orf79, NEDPBA
Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Parkinson disease

10632
6-pyruvoyltetrahydropterin synthase
PTPS
Hyperphenylalaninemia, Bipolar disorder, Metabolic syndrome

10633
PTTG1 regulator of sister chromatid separation, securin
EAP1, ECRAR, HPTTG, PTTG, TUTR1
Hepatocellular carcinoma, Psoriasis, Scoliosis, Sjogren syndrome

10634
PTTG1 interacting protein
C21orf1, C21orf3, PBF, PTTG1IP1
Ankylosing spondylitis, Cholecystolithiasis, Gallstones

10635
PTTG1IP family member 2
-
Retinopathy of prematurity

10636
Pentraxin 3
TNFAIP5, TSG-14
Cystic fibrosis, Depression, Dermatologic disorder, Major depressive disorder, Pulmonary fibrosis, Skin disease

10637
Pentraxin 4
C16orf38
Hemolytic anemia, Otosclerosis, Rheumatoid arthritis

10638
Pseudouridine 5'-phosphatase
DXF68S1E, FAM16AX, GS1, HDHD1, HDHD1A
Scoliosis

10639
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

10640
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