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"
71 to 80 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

71
Rac family small GTPase 2
EN-7, Gx, HSPC022, IMD73A, IMD73B, IMD73C, p21-Rac2
Celiac disease, Heart disease, Immunodeficiency, Myeloid leukemia, Lymphoma, Melanoma

72
Rac family small GTPase 3
-
Basal cell carcinoma, Desbuquois syndrome, Facial dysmorphism syndrome, Intellectual developmental disorder, Myeloid leukemia, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

73
Rac GTPase activating protein 1
CDAN3B, CYK4, HsCYK-4, ID-GAP, MgcRacGAP, RCGAP1
Congenital dyserythropoietic anemia, Hepatocellular carcinoma, Polycystic ovary syndrome

74
Receptor for activated C kinase 1
GNB2L1, Gnb2-rs1, H12.3, HLC-7, PIG21
Alzheimer disease, Bipolar disorder, Squamous cell carcinoma, Tourette syndrome, Mouth neoplasms, Neurodevelopmental disorder

75
RAD17 checkpoint clamp loader component
CCYC, HRAD17, R24L, RAD17SP, RAD24
Multiple sclerosis

76
RAD18 E3 ubiquitin protein ligase
RNF73
Color vision deficiency, Uterine fibroid

77
RAD21 cohesin complex component
CDLS4, HR21, HRAD21, MCD1, MGS, NXP1, SCC1, hHR21
Cornelia de lange syndrome, De lange syndrome, Desbuquois syndrome, Myeloid leukemia, Schizoaffective disorder, Trichorhinophalangeal syndrome

78
RAD21 cohesin complex component like 1
RAD21L, dJ545L17.2
Autoimmune thrombocytopenic purpura, Color vision deficiency, Multiple sclerosis, Oligodendroglioma, Testicular azoospermia

79
RAD23 nucleotide excision repair protein A
HHR23A, HR23A
Stomach neoplasms

80
RAD23 nucleotide excision repair protein B
HHR23B, HR23B, P58
Atrial fibrillation, Obstructive pulmonary disease, Craniofacial abnormalities, Male infertility, Alzheimer disease, Prostate cancer, Prostatic neoplasms