Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
1231 to 1240 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1231
Polypyrimidine tract binding protein 3
ROD1
Antiphospholipid syndrome, Cervical cancer, Colorectal cancer, Oligodendroglioma, Panic disorder, Schizophrenia

1232
Pentatricopeptide repeat domain 1
-
Metabolic syndrome, Nonalcoholic fatty liver disease, Diabetes mellitus, type 2

1233
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

1234
Pentatricopeptide repeat domain 3
COXPD51, MRP-S39, mS39
Combined oxidative phosphorylation deficiency, Leigh syndrome

1235
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)

1236
Patched 2
PTC2, SLC65B2
Basal cell carcinoma, Commissural facial cleft, Duplication of pituitary gland, Gastrointestinal stromal tumor, Gorlin syndrome, Medulloblastoma, Tessier facial cleft

1237
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

1238
Patched domain containing 3 (gene/pseudogene)
PTR, SLC65C3
Asthma, Colorectal cancer, Epilepsy, Inflammatory bowel disease, Rolandic epilepsy, Scoliosis

1239
Patched domain containing 4
C6orf138, PTCH53, SLC65C2, dJ402H5.2
Alzheimer disease, Colorectal cancer, Gastroesophageal reflux disease, Ovarian serous carcinoma

1240
Pre T cell antigen receptor alpha
IMD126, PT-ALPHA, PTA
Coronary artery disease, Immunodeficiency, Ocular sarcoidosis, Polycystic ovary syndrome