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
10421 to 10430 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10421
Prolactin receptor
HPRL, MFAB, RI-PRLR, hPRLrI
Autism, Breast cancer, Carcinoma, Chiari-frommel syndrome, Endometriosis, Hyperprolactinemia, Hyperproinsulinemia, Hyperthyroidism, Hypothyroidism, Liver cirrhosis, Premature ovarian failure, Schizophrenia

10422
Protamine 1
CT94.1, P1
Obesity

10423
Protein arginine methyltransferase 2
HRMT1L1
Diverticular disease, Scoliosis

10424
Protein arginine methyltransferase 3
HRMT1L3
Pancreatic cancer, Hypertension

10425
Protein arginine methyltransferase 5
HRMT1L5, HSL7, IBP72, JBP1, SKB1, SKB1Hs
Diffuse large b-cell lymphoma, Medulloblastoma, Multiple myeloma, Breast neoplasms

10426
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
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10427
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

10428
Protein arginine methyltransferase 8
HRMT1L3, HRMT1L4
Pelvic organ prolapse, Willis-ekbom disease

10429
Protein arginine methyltransferase 9
PRMT10
Intellectual developmental disorder dysmorphic behavioral, Neurodevelopmental disorder, Obesity

10430
Prion like protein doppel
DOPPEL, DPL, PrPLP, dJ1068H6.4
Creutzfeldt-jakob disease