Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "R"
271 to 280 of 577 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

271
RAB5B, member RAS oncogene family
-
Anorexia nervosa, Asthma, Eczema, Autoimmune disease, Basal cell carcinoma, Gastroesophageal reflux disease, Hashimoto disease, Hypothyroidism, Nasal polyp, Peptic ulcer disease, Polycystic ovary syndrome, Psoriasis, Rheumatoid arthritis, Diabetes mellitus, type 1, Diabetes mellitus, type 2
View all (1 more)

272
RAB27A, member RAS oncogene family
GS2, HsT18676, RAB27, RAM
Autoinflammatory syndrome, Central nervous system cancer, Glioma, Griscelli syndrome, Melanoma, Urinary bladder cancer

273
RAB27B, member RAS oncogene family
C25KG
Anxiety disorder, Asthma, Bipolar disorder, Gestational diabetes, Major depressive disorder, Metabolic syndrome, Mood disorder, Neurotic disorder, Obesity, Oligodendroglioma, Schizophrenia, Diabetes mellitus, type 2, Urinary bladder cancer, Uveal melanoma

274
RAB5C, member RAS oncogene family
L1880, RAB5CL, RAB5L, RABL
Autoimmune disease, Autoimmune thyroid disease, Coronary artery disease, Hypothyroidism, Intellectual developmental disorder, Vitiligo

275
Rac family small GTPase 1
MIG5, MRD48, Rac-1, TC-25, p21-Rac1
Alzheimer disease, Basal cell carcinoma, Hepatocellular carcinoma, Cardiomyopathy, Coronary artery disease, Major depressive disorder, Diabetes mellitus, Global developmental delay, Heart failure, Intellectual developmental disorder, Keratinocyte carcinoma, Liver disease, Melanoma, Depression, Metabolic syndrome
View all (4 more)

276
Rac family small GTPase 2
EN-7, Gx, HSPC022, IMD73A, IMD73B, IMD73C, p21-Rac2
Celiac disease, Heart disease, Immunodeficiency, Myeloid leukemia, Liver cirrhosis, Lymphoma, Melanoma

277
Rac family small GTPase 3
-
Basal cell carcinoma, Desbuquois syndrome, Facial dysmorphism syndrome, Intellectual developmental disorder, Myeloid leukemia, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

278
RAD9 checkpoint clamp component A
RAD9
Atrial fibrillation, Osteoarthritis

279
RAD21 cohesin complex component
CDLS4, HR21, HRAD21, MCD1, MGS, NXP1, SCC1, hHR21
Cornelia de lange syndrome, De lange syndrome, Desbuquois syndrome, Myeloid leukemia, Schizoaffective disorder, Trichorhinophalangeal syndrome

280
RAD23 nucleotide excision repair protein A
HHR23A, HR23A
Stomach neoplasms