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
10981 to 10990 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10981
RNA binding protein, mRNA processing factor
HERMES
Atrial fibrillation, Kidney cancer, Myeloproliferative disorder, Oropharyngeal cancer, Tonsil cancer, Uterine fibroid

10982
RNA binding protein, mRNA processing factor 2
-
Coronary artery disease

10983
Rabenosyn, RAB effector
KAREVS, MFANDO, Rabenosyn-5, ZFYVE20
Congenital neutropenia, Insomnia, Congenital myelofibrosis with anemia, Severe congenital neutropenia

10984
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

10985
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

10986
Ring finger and CCCH-type domains 2
MNAB, RNF164
Insomnia, Osteoarthritis

10987
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

10988
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

10989
RCC1 and BTB domain containing protein 1
CLLD7, CLLL7, GLP, RDEOA
Eczema, Exudative retinopathy, Exudative vitreoretinopathy, Multiple sclerosis, Retinitis pigmentosa, Schizophrenia, Systemic lupus erythematosus

10990
RCC1 like
WBSCR16
Williams syndrome