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
10931 to 10940 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10931
RNA binding protein, mRNA processing factor
HERMES
Atrial fibrillation, Kidney cancer, Myeloproliferative disorder, Oropharyngeal cancer, Tonsil cancer, Uterine fibroid

10932
RNA binding protein, mRNA processing factor 2
-
Coronary artery disease

10933
Rabenosyn, RAB effector
KAREVS, MFANDO, Rabenosyn-5, ZFYVE20
Congenital neutropenia, Insomnia, Congenital myelofibrosis with anemia, Severe congenital neutropenia

10934
Ring-box 1
BA554C12.1, RNF75, ROC1
Crohn disease, Inflammatory bowel disease, Insomnia, Major depressive disorder, Neurotic disorder, Parkinson disease, Schizophrenia, Seasonal allergic rhinitis, Stevens-johnson syndrome

10935
Ring finger and CCCH-type domains 1
FHL6, IMDSHY, RNF198, ROQUIN
Dyslexia, Hemophagocytic lymphohistiocytosis, Insomnia, Metabolic syndrome, Psychiatric disorders, Willis-ekbom disease, Diabetes mellitus type 2

10936
Ring finger and CCCH-type domains 2
MNAB, RNF164
Insomnia, Osteoarthritis

10937
Regulator of calcineurin 1
ADAPT78, CSP1, DSC1, DSCR1, MCIP1, RCN1
Alzheimer disease, Rheumatoid arthritis, Hepatocellular carcinoma, Congenital heart disease, Craniofacial abnormalities, Down syndrome, Congenital heart defect, Huntington disease, Psoriasis

10938
Regulator of calcineurin 2
CSP2, DSCR1L1, MCIP2, RCN2, ZAKI-4, ZAKI4
Color vision deficiency, Metabolic syndrome, Neurotic disorder, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

10939
RCC1 and BTB domain containing protein 1
CLLD7, CLLL7, GLP, RDEOA
Eczema, Exudative retinopathy, Exudative vitreoretinopathy, Multiple sclerosis, Retinitis pigmentosa, Schizophrenia, Systemic lupus erythematosus

10940
RCC1 like
WBSCR16
Williams syndrome