Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10841 to 10850 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10841
Retinoic acid early transcript 1E
LETAL, N2DL-4, NKG2DL4, RAET1E2, RL-4, ULBP4, bA350J20.7
Autism

10842
Retinoic acid early transcript 1L
RAET1H, ULBP6
Basal cell carcinoma, Keratinocyte carcinoma

10843
Raf-1 proto-oncogene, serine/threonine kinase
CMD1NN, CRAF, NS5, Raf-1, c-Raf
Asthma, Breast neoplasms, Non-small-cell lung carcinoma, Epithelial ovarian carcinoma, Cardiac arrhythmia, Cardiofaciocutaneous syndrome, Dilated cardiomyopathy, Cardiomyopathy, Cardiovascular disease, Obstructive pulmonary disease, Costello syndrome, Desbuquois syndrome, Glioma, Hyperalgesia, Hypertrophic cardiomyopathy
View all (13 more)

10844
Recombination activating 1
RAG-1, RNF74
Brain infarction, Congenital cataract, Cerebral amyloid angiopathy, Ciliary dyskinesia, Combined cellular and humoral immune defects with granulomas, Combined immunodeficiency disease, Combined immunodeficiency with granulomatosis, Combined immunodeficiency with skin granulomas, Lewy body disease, Omenn syndrome, Prostatic neoplasms, Severe combined immunodeficiency

10845
Recombination activating 2
RAG-2
Experimental arthritis, Combined cellular and humoral immune defects with granulomas, Combined immunodeficiency with granulomatosis, Combined immunodeficiency with skin granulomas, Common variable immunodeficiency, Eosinophilia, Immunodeficiency, Nonalcoholic fatty liver disease, Omenn syndrome, Salla disease, Severe combined immunodeficiency

10846
Retinoic acid induced 1
SMCR, SMS
17p11.2 microduplication syndrome, Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Basal cell carcinoma, Coronary artery disease, Craniofacial abnormalities, Deafness, Developmental disability, Glioma, Growth disorder, Intellectual developmental disorder, Melanoma, Myocardial infarction, Neurodevelopmental disorder
View all (8 more)

10847
Retinoic acid induced 14
NORPEG, RAI13
Gout

10848
Retinoic acid induced 2
-
Congenital heart disease, Dextrocardia

10849
RAS like proto-oncogene A
HINCONS, RAL
Neurodevelopmental disorder, Desbuquois syndrome, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Diabetes mellitus type 1, Diabetes mellitus type 2

10850
RAS like proto-oncogene B
-
Autism, Breast cancer, Estrogen-receptor negative breast cancer, Prostate cancer