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
11071 to 11080 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11071
RHEB like 1
RHEBL1c
Attention deficit hyperactivity disorder, Bipolar disorder

11072
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)

11073
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)

11074
Ras homolog family member B
ARH6, ARHB, MST081, MSTP081, RHOH6
Scleroderma, Systemic sclerosis, Venous thromboembolism

11075
Rho related BTB domain containing 1
-
Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

11076
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

11077
Rho related BTB domain containing 3
-
Obstructive pulmonary disease, Scoliosis

11078
Ras homolog family member C
ARH9, ARHC, H9, RHOH9
Hypertension, Myocardial ischemia

11079
Ras homolog family member D
ARHD, RHOHP1, RHOM, Rho
Insomnia

11080
Ras homolog family member F, filopodia associated
ARHF, RIF
Coronary artery disease