Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10591 to 10600 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10591
Polypyrimidine tract binding protein 1
HNRNP-I, HNRNPI, HNRPI, PTB, PTB-1, PTB-T, PTB2, PTB3, PTB4, pPTB
Carcinoma, Glaucoma, Open angle glaucoma, Osteosarcoma

10592
Polypyrimidine tract binding protein 2
PTBLP, brPTB, nPTB
Anal polyp, Anorexia nervosa, Major depressive disorder, Metabolic syndrome, Obesity, Schizophrenia, Diabetes mellitus type 2

10593
Polypyrimidine tract binding protein 3
ROD1
Antiphospholipid syndrome, Cervical cancer, Colorectal cancer, Oligodendroglioma, Panic disorder, Schizophrenia

10594
Pentatricopeptide repeat domain 1
-
Metabolic syndrome, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

10595
Pentatricopeptide repeat domain 2
-
Alzheimer disease, Ankylosing spondylitis, Asthma, Central nervous system cancer, Crohn disease, Eye disease, Glaucoma, Glioblastoma, Glioma, Hypothyroidism, Inflammatory bowel disease, Psoriasis, Respiratory system disease, Sclerosing cholangitis, Ulcerative colitis

10596
Pentatricopeptide repeat domain 3
COXPD51, MRP-S39, mS39
Combined oxidative phosphorylation deficiency, Leigh syndrome

10597
Patched 1
BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH, SLC65B1
Anophthalmia/microphthalmia-esophageal atresia syndrome, Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Basal cell carcinoma, Basal cell nevus syndrome, Brain neoplasms, Breast cancer, Cataract, Central nervous system infection, Obstructive pulmonary disease, Cleft lip, Cleft palate, Complete unilateral cleft lip
View all (34 more)

10598
Patched 2
PTC2, SLC65B2
Basal cell carcinoma, Commissural facial cleft, Duplication of pituitary gland, Gastrointestinal stromal tumor, Gorlin syndrome, Medulloblastoma, Tessier facial cleft

10599
Patched domain containing 1
AUTSX4, CXDELp22.11, DELXP22.11, SLC65C1
Atrial fibrillation, Autism, Autism, x-linked, Cardiac arrhythmia, Developmental disability, Intellectual developmental disorder, Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, X-linked intellectual disability, Depression

10600
Patched domain containing 3 (gene/pseudogene)
PTR, SLC65C3
Asthma, Colorectal cancer, Epilepsy, Inflammatory bowel disease, Rolandic epilepsy, Scoliosis