Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "R"
101 to 110 of 759 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

101
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

102
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
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103
Retinoic acid induced 14
NORPEG, RAI13
Gout

104
Retinoic acid induced 2
-
Congenital heart disease, Dextrocardia

105
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

106
RAS like proto-oncogene B
-
Autism, Breast cancer, Estrogen-receptor negative breast cancer, Prostate cancer

107
RalA binding protein 1
RIP1, RLIP1, RLIP76
Hypertension, Myocardial ischemia, Prostate cancer, Prostatic neoplasms

108
Ral GTPase activating protein catalytic subunit alpha 1
GARNL1, GRIPE, NEDHRIT, RalGAPalpha1, TULIP1, p240
Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Schizophrenia

109
Ral GTPase activating protein catalytic subunit alpha 2
AS250, C20orf74, bA287B20.1, dJ1049G11, dJ1049G11.4, p220
Small vessel stroke

110
Ral GTPase activating protein non-catalytic subunit beta
KIAA1219, RalGAPbeta
Neurodevelopmental disorder, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Scoliosis, Septo-optic dysplasia, Myopia