Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10051 to 10060 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10051
Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1
EDS6, EDSKCL1, LH, LH1, LLH, PLOD
Alzheimer disease, Byzanthine arch palate, Congenital contractural arachnodactyly, Congenital omphalocele, Deep vein thrombosis, Desbuquois syndrome, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Hydrocephalus, Keratoconus, Mitral valve prolapse, Moyamoya disease, Myopathy, Osteoarthritis, Psoriasis
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10052
Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2
BRKS2, LH2, TLH
Juvenile arthritis, Bone fragility with contractures, arterial rupture, and deafness, Bone neoplasms, Bowed long bones, Bruck syndrome, Buruli ulcer, Cleft palate, Congenital camptodactyly, Congenital clubfoot, Congenital hypoplasia of femur, Desbuquois syndrome, Juvenile idiopathic arthritis, Liver cirrhosis, Obesity, Osteoarthritis
View all (4 more)

10053
Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
BCARD, LH3
Bone fragility with contractures, arterial rupture, and deafness, Cerebral amyloid angiopathy, Connective tissue disease, Larsen syndrome, Marshall syndrome, Osteoporosis-pseudoglioma syndrome

10054
Proteolipid protein 1
GPM6C, HLD1, MMPL, PLP, PLP/DM20, PMD, SPG2
Auditory neuropathy, Intellectual developmental disorder, Pelizaeus-merzbacher disease, Schizophrenia, Spastic paraplegia, x-linked, Spastic paraplegia, Hereditary spastic paraplegia

10055
Pyridoxal phosphate binding protein
EPEO1, EPVB6D, PROSC
Early onset vitamin b6 dependent epilepsy, Pyridoxine dependent epilepsy, Pyridoxine-dependent epilepsy

10056
Phospholipid phosphatase 1
LLP1a, LPP1, PAP-2a, PAP2, PPAP2A
Stomach neoplasms, Diabetes mellitus type 1

10057
Phospholipid phosphatase 2
LPP2, PAP-2c, PAP2-g, PPAP2C
Liver cirrhosis, Peripheral arterial disease

10058
Phospholipid phosphatase 3
Dri42, LPP3, PAP2B, PPAP2B, VCIP
Atrial fibrillation, Cardiomegaly, Cardiovascular disease, Ischemic heart disease, Coronary artery disease, Crohn disease, Eosinophilia, Gout, Heart disease, Heart failure, Inflammatory bowel disease, Large artery stroke, Metabolic syndrome, Colorectal adenoma, Myocardial infarction
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10059
Phospholipid phosphatase 4
DPPL2, PPAPDC1, PPAPDC1A
Alzheimer disease, Bipolar disorder, Color vision deficiency, Major depressive disorder, Parkinson disease, Schizophrenia

10060
Phospholipid phosphatase 7 (inactive)
C9orf67, NET39, PPAPDC3
Alzheimer disease, Central nervous system cancer, Glioblastoma, Glioma, Gout