731
|
|
|
Rubicon autophagy regulator |
KIAA0226, RUBICON, SCAR15 |
|
732
|
|
|
Rubicon like autophagy enhancer |
C13orf18, KIAA0226L, PACER |
|
733
|
|
|
RUN and FYVE domain containing 1 |
RABIP4, ZFYVE12 |
|
734
|
|
|
RUN and FYVE domain containing 2 |
RABIP4R, ZFYVE13 |
|
735
|
|
|
RUN and FYVE domain containing 3 |
RIPX, SINGAR1, ZFYVE30 |
|
736
|
|
|
RUN and FYVE domain containing 4 |
ZFYVE31 |
|
737
|
|
|
RUN domain containing 3B |
RPIB9, RPIP9 |
|
738
|
|
|
RUNX family transcription factor 1 |
AML1, AML1-EVI-1, AMLCR1, CBF2alpha, CBFA2, EVI-1, PEBP2aB, PEBP2alpha |
Myeloid leukemia, Androgenetic alopecia, Angioedema, Rheumatoid arthritis, Asthma, Atrial fibrillation, Platelet disorder, Burkitt lymphoma, Celiac disease, Clonal cytopenia of undetermined significance, Clonal hematopoiesis, Dementia, Endometriosis, Esophageal cancer, Esophageal squamous cell carcinoma, Glaucoma, Glioblastoma, Lung cancer, Migraine, Myelodysplastic syndrome, Myeloproliferative disorder, Myocardial infarction, Obesity, Oligoarticular juvenile idiopathic arthritis, Open angle glaucoma, Pancytopenia, Polyarticular juvenile idiopathic arthritis, Preeclampsia, Prostatic neoplasms, Psoriasis, Respiratory system disease, Stroke, Juvenile idiopathic arthritis, Thrombocytopenia, Transient myeloproliferative disorder, Hypertension, Uterine fibroidView all (22 more) |
739
|
|
|
RUNX1 partner transcriptional co-repressor 1 |
AML1-MTG8, AML1T1, CBFA2T1, CDR, ETO, MTG8, ZMYND2 |
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cannabis abuse, Basal cell carcinoma, Obstructive pulmonary disease, Color vision deficiency, Erectile dysfunction, Gout, Insomnia, Myeloid leukemia, Malunion fracture, Metabolic syndrome, Neurodevelopmental disorder, Oligodendroglioma, Osteoarthritis, Peptic ulcer disease, Schizophrenia, Scoliosis, Small cell lung carcinoma, Substance abuse, Tourette syndrome, Hypertension, Diabetes mellitus type 2View all (9 more) |
740
|
|
|
RUNX family transcription factor 2 |
AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD, OSF-2, OSF2, PEA2aA, PEBP2aA |
Alzheimer disease, Androgenetic alopecia, Psoriatic arthritis, Rheumatoid arthritis, Breast neoplasms, Obstructive pulmonary disease, Cleidocranial dysplasia, Color vision deficiency, Colorectal cancer, Coronary artery disease, Craniofacial abnormalities, Craniosynostosis, Dementia, Desbuquois syndrome, Gout, Hodgkin lymphoma, Metaphyseal dysplasia, Nephrotic syndrome, Open angle glaucoma, Orofacial cleft, Osteoarthritis, Osteosarcoma, Pancreatic cancer, Periodontitis, Progressive supranuclear palsy, Substance abuse, Tooth abnormalities, UremiaView all (13 more) |
