Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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
Showing genes starting with "R"
441 to 450 of 759 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

441
Relaxin 2
H2, H2-RLX, RLXH2, bA12D24.1.1, bA12D24.1.2
Clonal hematopoiesis, Prostatic neoplasms, Ulcerative colitis

442
Relaxin 3
H3, RXN3, ZINS4, insl7
Hyperplasia, Myocardial ischemia, Obesity

443
Regulator of MON1-CCZ1
C18orf8, HsT2591, MIC1, Mic-1, WDR98
Atrial fibrillation, Metabolic syndrome, Niemann-pick disease, Diabetes mellitus type 2

444
Regulator of microtubule dynamics 2
BLOCK18, FAM82A, FAM82A1, PRO34163, PYST9371, RMD-2, RMD2, RMD4
Alzheimer disease, Neoplasms, Melanoma, Erectile dysfunction, Esophageal cancer, Gastric cancer, Liver cirrhosis, Mouth neoplasms, Prostate cancer, Psychiatric disorders

445
RecQ mediated genome instability 1
BLAP75, C9orf76, FAAP75
Attention deficit hyperactivity disorder, Cannabis abuse, Color vision deficiency, Migraine, Multiple system atrophy, Schizophrenia, Substance abuse, Diabetes mellitus type 2

446
RecQ mediated genome instability 2
BLAP18, C16orf75
Ankylosing spondylitis, Asthma, Autoimmune disease, Bulimia, Celiac disease, Cholecystolithiasis, Colorectal cancer, Crohn disease, Dementia, Gallstones, Inflammatory bowel disease, Leprosy, Multiple sclerosis, Obesity, Oligoarticular juvenile idiopathic arthritis
View all (13 more)

447
Required for meiotic nuclear division 1 homolog
C6orf96, COXPD11, RMD1, bA351K16, bA351K16.3
Breast neoplasms, Combined oxidative phosphorylation deficiency, Congenital neurologic anomalies, Mitochondrial disease, Nephronophthisis, Perrault syndrome, Uterine fibroid, Xx gonadal dysgenesis syndrome

448
Required for meiotic nuclear division 5 homolog A
CTLH, GID2, GID2A, RMD5, p44CTLH
Hypertrophic cardiomyopathy, Rheumatoid arthritis, Schizophrenia

449
Required for meiotic nuclear division 5 homolog B
GID2, GID2B
Dyskeratosis congenita, Liver cirrhosis

450
Ribonuclease MRP subunit p64
ANXD3, C3orf17, NEPRO, NET17
Anauxetic dysplasia