Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11131 to 11140 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11131
Ring finger protein, LIM domain interacting
MRX61, NY-REN-43, RNF12, TOKAS
Global developmental delay, Intellectual developmental disorder, x-linked, Non-specific syndromic intellectual disability, X-linked intellectual disability, Prostatic neoplasms, Tonne-kalscheuer syndrome

11132
Relaxin 1
H1, H1RLX, RLXH1, bA12D24.3.1, bA12D24.3.2
Hypertrophy

11133
Relaxin 2
H2, H2-RLX, RLXH2, bA12D24.1.1, bA12D24.1.2
Clonal hematopoiesis, Prostatic neoplasms, Ulcerative colitis

11134
Relaxin 3
H3, RXN3, ZINS4, insl7
Hyperplasia, Myocardial ischemia, Obesity

11135
Regulator of MON1-CCZ1
C18orf8, HsT2591, MIC1, Mic-1, WDR98
Atrial fibrillation, Metabolic syndrome, Niemann-pick disease, Diabetes mellitus type 2

11136
Regulator of microtubule dynamics 2
BLOCK18, FAM82A, FAM82A1, PRO34163, PYST9371, RMD-2, RMD2, RMD4
Alzheimer disease, Neoplasms, Melanoma, Erectile dysfunction, Esophageal cancer, Gastric cancer, Mouth neoplasms, Prostate cancer, Psychiatric disorders

11137
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

11138
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, Multiple sclerosis, Obesity, Oligoarticular juvenile idiopathic arthritis, Oligodendroglioma
View all (12 more)

11139
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

11140
Required for meiotic nuclear division 5 homolog A
CTLH, GID2, GID2A, RMD5, p44CTLH
Hypertrophic cardiomyopathy, Rheumatoid arthritis, Schizophrenia