Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "R"
161 to 170 of 577 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

161
Regulator of cell cycle
C13orf15, RGC-32, RGC32, bA157L14.2
Myocardial ischemia

162
RAN guanine nucleotide release factor
HSPC165, HSPC236, MOG1, RANGNRF
Atrioventricular block, Brugada syndrome, Bundle branch block, Lung adenocarcinoma, Paroxysmal ventricular tachycardia, Sick sinus syndrome, Supraventricular tachycardia, Trifascicular block, Ventricular fibrillation

163
Rac GTPase activating protein 1
CDAN3B, CYK4, HsCYK-4, ID-GAP, MgcRacGAP, RCGAP1
Liver carcinoma, Sclerocystic ovaries, Polycystic ovary syndrome

164
Retina and anterior neural fold homeobox
MCOP3, MCOPS16, RAX1, RX
Congenital ankyloblepharon, Isolated microphthalmia-anophthalmia-coloboma, Melanoma, Microphthalmia, Microphthalmos, Sclerocornea, Syndromic microphthalmia

165
Rieske Fe-S domain containing
-
Bipolar disorder, Mental depression, Schizophrenia

166
RAB37, member RAS oncogene family
-
Coronary artery disease

167
Replication protein A2 pseudogene 1
RPA2P
Parkinson disease

168
RAB7B, member RAS oncogene family
RAB7
Coronary syndrome, Osteoporosis

169
R-spondin 2
CRISTIN2, HHRRD, TETAMS2
Agenesis of corpus callosum, Alopecia, Alopecia, male pattern, Androgenetic alopecia, Ankyloglossia, Atresia of vagina, Cataract, Congenital coloboma of iris, Congenital diaphragmatic hernia, Short clavicles, Cryptorchidism, Glossoptosis, Humerofemoral hypoplasia with radiotibial ray deficiency, Hydrocephalus, Imperforate anus
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170
RD3 regulator of GUCY2D
C1orf36, LCA12
Cataract, Ciliopathies, Congenital blindness, Congenital cerebral hernia, Developmental delay, Disorder of eye, Hemiplegia/hemiparesis, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Nystagmus