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"
321 to 330 of 759 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
-
Dry eye syndrome, Prostate cancer

322
Ret finger protein like 2
RNF79
Oligodendroglioma, Polycystic ovary syndrome, Diabetes mellitus type 2

323
Ret finger protein like 4A
RFPL4, RNF210
Major depressive disorder

324
Ret finger protein like 4B
RNF211
Oligodendroglioma

325
RFT1 glycolipid translocator homolog
CDG1N, SLC76A1
Attention deficit hyperactivity disorder, Autism, Congenital disorder of glycosylation, Coronary artery disease, Crohn disease, Gout, Inflammatory bowel disease, Metabolic syndrome, Multiple sclerosis, Schizophrenia, Diabetes mellitus type 2

326
Raftlin, lipid raft linker 1
MIG2, PIB10, PIG9, RAFTLIN
Female infertility, Obesity, Thoracic aortic aneurysm

327
Raftlin family member 2
C2orf11, Raftlin-2
Asthma, Bipolar disorder, Crohn disease, Dilated cardiomyopathy, Dyslexia, Inflammatory bowel disease, Insomnia, Major depressive disorder, Pancreatic cancer, Psoriasis, Schizophrenia, Skin cancer, Stroke, Systemic lupus erythematosus

328
Ring finger and WD repeat domain 3
FANCW, RNF201
Fanconi anemia, Tourette syndrome, Multiple myeloma, Testicular carcinoma, Testicular germ cell tumor

329
Regulatory factor X2
-
Alzheimer disease, Bipolar disorder, Cerebral palsy, Major depressive disorder, Schizophrenia, Tooth agenesis

330
Regulatory factor X3
-
Attention deficit hyperactivity disorder, Atypical femoral fracture, Autism, Neurodevelopmental disorder, Dementia, Dermatologic disorder, Developmental disability, Insomnia, Non-specific syndromic intellectual disability, Oligodendroglioma, Prostate cancer, Schizophrenia, Scoliosis, Skin disease, Diabetes mellitus type 2