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 "R"
291 to 300 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

291
RALBP1 associated Eps domain containing 2
POB1
Breast neoplasms, Clear cell renal cell carcinoma, Developmental and epileptic encephalopathy, Kidney cancer

292
Retention in endoplasmic reticulum sorting receptor 1
-
Peroxisome biogenesis disorder

293
Arginine-glutamic acid dipeptide repeats
ARG, ARP, ATN1L, DNB1, NEDBEH
1p36 deletion syndrome, Alzheimer disease, Androgenetic alopecia, Anorexia nervosa, Juvenile arthritis, Asthma, Eczema, Attention deficit hyperactivity disorder, Autism, Autoimmune thyroid disease, Bipolar disorder, Cardiovascular disease, Charge syndrome, Chromosome 1p36 deletion syndrome, Obstructive pulmonary disease
View all (25 more)

294
RAS like estrogen regulated growth inhibitor
-
Alzheimer disease, Kidney disease, Obstructive pulmonary disease, Endometriosis, Gastroesophageal reflux disease, Gout, Raynaud disease

295
RERG like
-
Alzheimer disease, Kidney disease, Head and neck neoplasm, Insomnia, Lung cancer, Major depressive disorder, Oropharyngeal cancer, Scoliosis, Upper aerodigestive tract neoplasm

296
Retroelement silencing factor 1
C12orf35, GET, KIAA1551, UTA2-1
Alzheimer disease, Breast cancer, Dementia, Obesity, Ocular sarcoidosis, Testicular carcinoma, Testicular germ cell tumor

297
Regulated endocrine specific protein 18
-
Metabolic syndrome, Diabetes mellitus type 2

298
RE1 silencing transcription factor
DFNA27, GINGF5, HGF5, NRSF, WT6, XBR
Atrial fibrillation, Attention deficit hyperactivity disorder, Nonsyndromic hearing loss, Coronary artery disease, Deafness, Glaucoma, Major depressive disorder, Migraine, Myocardial infarction, Osteoarthritis, Schizophrenia, Seizures, Substance abuse, Wilms tumor

299
Ret proto-oncogene
CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1, PTC, RET-ELE1
Alzheimer disease, Amyloidosis, Appendicitis, Renal agenesis, Burkitt lymphoma, Congenital anomalies of the kidney and urinary tract, Medullary carcinoma, Haddad syndrome, Colorectal neoplasms, Congenital central hypoventilation syndrome, Congenital digestive system anomaly, Congenital hypoplasia of kidney, Differentiated thyroid carcinoma, Hirschsprung disease, Hypothyroidism
View all (8 more)

300
Resistin
ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1
Autism, Congestive heart failure, Diabetes mellitus type 2, Heart failure, Hypertension, Hypertrophic cardiomyopathy, Kidney failure, Promyelocytic leukemia, Metabolic syndrome, Obesity