Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "R"

141 to 150 of 759 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
141	51195	RAPGEFL1	Rap guanine nucleotide exchange factor like 1	Link-GEFII	Bronchitis, Cold autoinflammatory syndrome, Osteoarthritis, Respiratory system disease
142	65059	RAPH1	Ras association (RalGDS/AF-6) and pleckstrin homology domains 1	ALS2CR18, ALS2CR9, LPD, PREL-2, PREL2, RMO1, RalGDS/AF-6	Coronary artery disease, Diverticular disease, Major depressive disorder, Myocardial infarction, Osteoarthritis, Systemic lupus erythematosus, Depression
143	5913	RAPSN	Receptor associated protein of the synapse	CMS11, CMS4C, FADS, FADS2, RAPSYN, RNF205	Alzheimer disease, Ankylosing spondylitis, Arthrogryposis multiplex congenita, Autoimmune disease, Congenital myasthenic syndrome, Fetal akinesia deformation sequence, Glaucoma, Global developmental delay, Hydrops fetalis, Major depressive disorder, Mood disorder, Obesity, Myasthenic syndrome, Myopathy, Neuromuscular disease View all (7 more)
144	5914	RARA	Retinoic acid receptor alpha	NR1B1, RAR, RARalpha	Breast neoplasms, Hepatocellular carcinoma, Central nervous system cancer, Dyslipidemias, Glioblastoma, Glioma, Promyelocytic leukemia, Mood disorder, Orofacial cleft, Schizophrenia
145	5915	RARB	Retinoic acid receptor beta	HAP, MCOPS12, NR1B2, RARbeta, RARbeta1, RRB2	Alzheimer disease, Anophthalmia, Asthma, Astrocytoma, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bell's palsy, Biliary cirrhosis, Bipolar disorder, Breast neoplasms, Squamous cell carcinoma, Cataract, Obstructive pulmonary disease, Color vision deficiency View all (29 more)
146	5916	RARG	Retinoic acid receptor gamma	NR1B3, RARC, RARgamma	Cleft palate, Congenital musculoskeletal anomalies, Gout, Heart disease, Schizophrenia
147	5918	RARRES1	Retinoic acid receptor responder 1	LXNL, PERG-1, TIG1	Asthma, Liver cirrhosis, Stomach neoplasms
148	5919	RARRES2	Retinoic acid receptor responder 2	HP10433, TIG2	Preeclampsia
149	5917	RARS1	Arginyl-tRNA synthetase 1	ArgRS, DALRD1, HLD9, RARS	Hypomyelinating leukodystrophy, Leukodystrophy
150	57038	RARS2	Arginyl-tRNA synthetase 2, mitochondrial	ArgRS, DALRD2, PCH6, PRO1992, RARSL	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Neurodevelopmental disorder, Congenital disorder of glycosylation, Mitochondrial disease, Non-specific syndromic intellectual disability, Pontocerebellar hypoplasia

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