Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "P"
771 to 780 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

771
Podocalyxin like
Gp200, PC, PCLP, PCLP-1, PDX, PODXL1, gp135
Juvenile parkinsonism, Carotid artery disease, Hemorrhage, Hypertension, Nephrotic syndrome, Parkinson disease, Hereditary parkinson disease, Prostatic neoplasms, Thrombosis

772
POF1B actin binding protein
POF, POF2B
Dyslexia, Premature ovarian failure

773
Protein O-fucosyltransferase 1
DDD2, FUT12, O-FUT, O-Fuc-T, O-FucT-1, OFUCT1
Ankylosing spondylitis, Asthma, Obstructive pulmonary disease, Neurodevelopmental disorder, Congenital disorder of glycosylation, Crohn disease, Dowling degos disease, Inflammatory bowel disease, Insomnia, Non-specific syndromic intellectual disability, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

774
Pogo transposable element derived with KRAB domain
BASS2, KRBOX2, LST003
Insomnia, Osteoarthritis, Post-traumatic stress disorder

775
Protein O-glucosyltransferase 1
C3orf9, CLP46, KDELCL1, KTELC1, LGMD2Z, LGMDR21, MDS010, MDSRP, Rumi, hCLP46
Limb girdle muscular dystrophy, Biliary cirrhosis, Dowling degos disease, Limb-girdle muscular dystrophy, Biliary cholangitis

776
Protein O-glucosyltransferase 3
KDELC2
Breast cancer, Clonal hematopoiesis, Estrogen-receptor negative breast cancer, Melanoma, Prostate cancer, Triple negative breast cancer, Uterine fibroid

777
Pogo transposable element derived with ZNF domain
MRD37, WHSUS, ZNF280E, ZNF635, ZNF635m
Apraxia, Autism, Brachycephaly, Byzanthine arch palate, Global developmental delay, Hearing impairment, Hypothyroidism, Intellectual developmental disorder, Intellectual developmental disorder microcephaly strabismus behaviora, Myopia, Neurodevelopmental disorder, Obesity, Hearing loss, Strabismus, White sutton syndrome

778
DNA polymerase alpha 1, catalytic subunit
NSX, PDR, POLA, VEODS, p180
Insomnia, Post-traumatic stress disorder, Aplastic anemia, , X-linked intellectual disability, X-linked reticulate pigmentary disorder

779
DNA polymerase alpha 2, accessory subunit
-
Colorectal cancer, Hyperuricemia, Pancreatic cancer, Telomere syndrome

780
DNA polymerase beta
-
Colonic neoplasms, Lymphocytic b-cell leukemia, Urinary bladder neoplasms