Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "P"
1051 to 1060 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1051
Prolactin
GHA1
Amenorrhea, Anemia, Autism, Basal ganglia disease, Bradycardia, Carotid artery disease, Catalepsy, Chiari-frommel syndrome, Congestive heart failure, Disruptive impulse-control and conduct disorder, Endometriosis, Erectile dysfunction, Growth hormone-secreting pituitary adenoma, Heart failure, Hyperproinsulinemia
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1052
Prolactin releasing hormone receptor
GPR10, GR3, PrRPR
Hypertension, Uterine fibroid

1053
Prolactin receptor
HPRL, MFAB, RI-PRLR, hPRLrI
Autism, Breast cancer, Carcinoma, Chiari-frommel syndrome, Endometriosis, Hyperprolactinemia, Hyperproinsulinemia, Hyperthyroidism, Hypothyroidism, Premature ovarian failure, Schizophrenia

1054
Protamine 1
CT94.1, P1
Obesity

1055
Protein arginine methyltransferase 2
HRMT1L1
Diverticular disease, Scoliosis

1056
Protein arginine methyltransferase 3
HRMT1L3
Pancreatic cancer, Hypertension

1057
Protein arginine methyltransferase 5
HRMT1L5, HSL7, IBP72, JBP1, SKB1, SKB1Hs
Diffuse large b-cell lymphoma, Medulloblastoma, Multiple myeloma, Breast neoplasms

1058
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, Lung cancer, Metabolic syndrome, Non-hodgkins lymphoma, Ovarian cancer
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1059
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

1060
Protein arginine methyltransferase 8
HRMT1L3, HRMT1L4
Pelvic organ prolapse, Willis-ekbom disease