Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10331 to 10340 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10331
Proteoglycan 3, pro eosinophil major basic protein 2
MBP2, MBPH
Hypertrophic cardiomyopathy

10332
Proteoglycan 4
CACP, HAPO, JCAP, MSF, SZP
Arthrogryposis multiplex congenita, Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, Contracture, Hyperplasia, Pena-shokeir syndrome , Pericarditis, Secondary malignant neoplasm

10333
Prickle planar cell polarity protein 1
EPM1B, RILP
Alzheimer disease, Arthrogryposis multiplex congenita, Autoimmune thyroid disease, Epilepsy, Progressive myoclonic epilepsy, Rolandic epilepsy, Graves disease, Hashimoto disease, Intellectual developmental disorder, Multiple sclerosis, Pena-shokeir syndrome , Unverricht-lundborg syndrome

10334
Prickle planar cell polarity protein 2
EPM5
Alzheimer disease, Asthma, Nonsyndromic intellectual disability, Endocrine neoplasms, Breast cancer, Colorectal cancer, Neurodevelopmental disorder, Dementia, Digestive system disease, Rolandic epilepsy, Generalized anxiety disorder, Glaucoma, Hyperopia, Liver neoplasms, Myoclonic epilepsy
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10335
Prickle planar cell polarity protein 3
LMO6, LOAM, LOAS, Pk3
Leber hereditary optic neuropathy

10336
Prickle planar cell polarity protein 4
C6orf49, OBTP, OEBT, TOMM6
Insomnia

10337
DNA primase subunit 1
PDIL, p49
Breast cancer, Obstructive sleep apnea syndrome, Premature ovarian failure, Seckel syndrome, Diabetes mellitus type 2, Uterine fibroid, Uterine polyp

10338
DNA primase subunit 2
PRIM2A, p58
Alzheimer disease, Coronary artery disease, Myocardial infarction, Myocardial ischemia, Scoliosis, Systemic lupus erythematosus

10339
Proline rich membrane anchor 1
PRIMA
Obstructive pulmonary disease, Epilepsy, Gestational diabetes, Insomnia, Major depressive disorder, Muscular dystrophy, Oligodendroglioma, Depression

10340
Primase and DNA directed polymerase
CCDC111, MYP22, Primpol1
Myopia, Retinitis pigmentosa