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
11121 to 11130 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11121
Ras homolog, mTORC1 binding
RHEB2
Non-small-cell lung carcinoma, Central nervous system cancer, Neurodevelopmental disorder, Focal cortical dysplasia, Glioblastoma, Glioma, Hemimegalencephaly, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Oligodendroglioma

11122
RHEB like 1
RHEBL1c
Attention deficit hyperactivity disorder, Bipolar disorder

11123
Rhodopsin
CSNBAD1, OPN2, RP4
Retinitis pigmentosa, Blindness, Cataract, Cone dystrophy, Cone-rod dystrophy, Congenital stationary night blindness, Exudative retinopathy, Microcephaly, Neuropathy, congenital hypomyelinating, Night blindness, congenital stationary, Nystagmus, Oguchi disease, Optic atrophy, Retinal degeneration, Retinal detachment
View all (3 more)

11124
Ras homolog family member A
ARH12, ARHA, EDFAOB, RHO12, RHOH12
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Carcinoma, Congenital hemihypertrophy, Coronary artery disease, Craniofacial abnormalities, Ectodermal dysplasia, Gout, Inflammatory bowel disease, Myocardial infarction, Proteinuria, Stomach neoplasms, Substance abuse, Tooth disease
View all (1 more)

11125
Ras homolog family member B
ARH6, ARHB, MST081, MSTP081, RHOH6
Scleroderma, Systemic sclerosis, Venous thromboembolism

11126
Rho related BTB domain containing 1
-
Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

11127
Rho related BTB domain containing 2
DBC2, DEE64, EIEE64, p83
Basal cell carcinoma, Chorea, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Non-neoplastic peripheral nervous system disease, Non-specific syndromic intellectual disability, Peripheral nervous system disease, Peripheral neuropathy, Rett syndrome

11128
Rho related BTB domain containing 3
-
Obstructive pulmonary disease, Scoliosis

11129
Ras homolog family member C
ARH9, ARHC, H9, RHOH9
Hypertension, Myocardial ischemia

11130
Ras homolog family member D
ARHD, RHOHP1, RHOM, Rho
Insomnia