Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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

10441 to 10450 of 15448 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
10441	128674	PROKR2	Prokineticin receptor 2	GPR73L1, GPR73b, GPRg2, HH3, KAL3, PKR2, dJ680N4.3	Amphetamine or sympathomimetic abuse, Bipolar disorder, Desbuquois syndrome, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Male infertility single gene azoospermia, Male infertility spermatogenesis disorder, Mood disorder, Neurodevelopmental disorder, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Pituitary stalk interruption syndrome View all (2 more)
10442	8842	PROM1	Prominin 1	AC133, CD133, CORD12, MCDR2, MSTP061, PROML1, RP41, STGD4	Leber congenital amaurosis, Retinitis pigmentosa, Brain aneurysm, Transitional cell carcinoma, Kidney disease, Colonic neoplasms, Color vision deficiency, Colorectal neoplasms, Cone-rod dystrophy, Dental caries, Diabetic neuropathy, Dilated cardiomyopathy, Glioblastoma, Heart failure, Hypertrophic cardiomyopathy View all (9 more)
10443	5626	PROP1	PROP paired-like homeobox 1	CPHD2, PROP-1	Combined pituitary hormone deficiency, Desbuquois syndrome, Genetic panhypopituitarism, Hypogonadism, Hypopituitarism, Hypothyroidism, Panhypopituitarism, Pituitary dwarfism, Pituitary hormone deficiency
10444	9692	PRORP	Protein only RNase P catalytic subunit	COXPD54, KIAA0391, MRPP3	Eczema, Biliary cirrhosis, Breast cancer, Childhood-onset sensorineural hearing impairment, Combined oxidative phosphorylation deficiency, Crohn disease, Global developmental delay, Inflammatory bowel disease, Mitochondrial disease, Perrault syndrome, Biliary cholangitis, Psoriasis, Schizophrenia, Xx gonadal dysgenesis syndrome
10445	5627	PROS1	Protein S	PROS, PS21, PS22, PS23, PS24, PS25, PSA, THPH5, THPH6	Juvenile arthritis, Ischemic stroke, Clear cell renal cell carcinoma, Deep vein thrombosis, Heart disease, Juvenile idiopathic arthritis, Kidney cancer, Optic atrophy, Oligoarticular juvenile idiopathic arthritis, Cerebral venous sinus thrombosis, Stevens-johnson syndrome, Thrombocytopenia, Thromboembolism, Thrombophilia, Thrombosis, Venous thromboembolism View all (1 more)
10446	80209	PROSER1	Proline and serine rich 1	C13orf23	Neurodevelopmental disorder
10447	254427	PROSER2	Proline and serine rich 2	C10orf47	Bone fracture, Breast cancer, Estrogen-receptor negative breast cancer
10448	148137	PROSER3	Proline and serine rich 3	C19orf55	Breast cancer, Cataract, Prostate cancer
10449	5629	PROX1	Prospero homeobox 1	-	Congenital heart disease, Diabetes mellitus, Diabetes mellitus type 2, Diabetic neuropathy, Diabetic retinopathy, Female infertility, Polycystic ovary syndrome, Psoriasis
10450	283571	PROX2	Prospero homeobox 2	PROX-2	Obstructive pulmonary disease, Neurotic disorder

«««...1043 104410451046 1047...»»»