Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
10131 to 10140 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10131
POC5 centriolar protein
C5orf37
Anorexia nervosa, Atrial fibrillation, Attention deficit hyperactivity disorder, Cancer, Coronary artery disease, Diabetes mellitus, Heart failure, Metabolic syndrome, Migraine, Obesity, Optic atrophy, Retinitis pigmentosa, Scoliosis, Stroke, Diabetes mellitus type 2

10132
Podocan like 1
SLRR5B
Lung cancer, Squamous cell carcinoma

10133
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

10134
POF1B actin binding protein
POF, POF2B
Dyslexia, Premature ovarian failure

10135
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

10136
Pogo transposable element derived with KRAB domain
BASS2, KRBOX2, LST003
Insomnia, Osteoarthritis, Post-traumatic stress disorder

10137
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

10138
Protein O-glucosyltransferase 3
KDELC2
Breast cancer, Clonal hematopoiesis, Estrogen-receptor negative breast cancer, Melanoma, Prostate cancer, Triple negative breast cancer, Uterine fibroid

10139
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

10140
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