Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
1061 to 1070 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1061
Protein arginine methyltransferase 2
HRMT1L1
Diverticular disease, Scoliosis

1062
Protein arginine methyltransferase 3
HRMT1L3
Pancreatic cancer, Hypertension

1063
Protein arginine methyltransferase 5
HRMT1L5, HSL7, IBP72, JBP1, SKB1, SKB1Hs
Diffuse large b-cell lymphoma, Medulloblastoma, Multiple myeloma, Triple negative breast cancer

1064
Protein arginine methyltransferase 6
HRMT1L6
Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Gestational diabetes, Hepatocellular carcinoma, Leprosy, Lung cancer, Metabolic syndrome, Non-hodgkins lymphoma
View all (7 more)

1065
Protein arginine methyltransferase 7
SBIDDS
Brachydactyly, Congenital hypoplasia of kidney, Progressive myoclonic epilepsy, Developmental and epileptic encephalopathy, Hepatocellular carcinoma, Hyperlipidemia, Obesity, Schizophrenia, Intellectual disability, Skeletal dysplasia

1066
Protein arginine methyltransferase 8
HRMT1L3, HRMT1L4
Pelvic organ prolapse, Willis-ekbom disease

1067
Protein arginine methyltransferase 9
PRMT10
Intellectual developmental disorder dysmorphic behavioral, Neurodevelopmental disorder, Obesity

1068
Prion like protein doppel
DOPPEL, DPL, PrPLP, dJ1068H6.4
Creutzfeldt-jakob disease

1069
Prion protein (Kanno blood group)
ASCR, AltPrP, CD230, CJD, GSS, KURU, PRIP, PrP, PrP27-30, PrP33-35C, PrPc, p27-30
Alzheimer disease, Autism, Cerebral amyloid angiopathy, Depression, Creutzfeldt-jakob disease, , Vascular dementia, Major depressive disorder, Hepatolenticular degeneration, Huntington disease, Insomnia, Liver cirrhosis, Mood disorder, Multiple sclerosis, Necrosis
View all (3 more)

1070
Proline rich basic protein 1
C5orf65
Hypertrophic cardiomyopathy, Keratoconus