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"
31 to 40 of 759 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

31
RAB31, member RAS oncogene family
Rab22B
Alzheimer disease, Bone fracture, Colorectal cancer, Dupuytren contracture, Liver cirrhosis, Lung cancer

32
RAB32, member RAS oncogene family
PARK26
Allergic contact dermatitis, Differentiated thyroid carcinoma, Leprosy, Liver cirrhosis, Parkinson disease

33
RAB33A, member RAS oncogene family
RabS10
Auditory neuropathy, Autism, Beta-hydroxyisobutyryl-coa deacylase deficiency, Charcot-marie-tooth disease, Combined oxidative phosphorylation deficiency, Congenital ear anomaly, Cowchock syndrome, Deafness, x-linked, Leukodystrophy, Peripheral neuropathy, Hearing loss, Spondyloepimetaphyseal dysplasia

34
RAB33B, member RAS oncogene family
SMC2
Desbuquois syndrome, Smith-mccort dysplasia

35
RAB34, member RAS oncogene family
NARR, OFD20, RAB39, RAH
Jeune thoracic dystrophy, Orofaciodigital syndrome

36
RAB35, member RAS oncogene family
H-ray, RAB1C, RAY
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

37
RAB37, member RAS oncogene family
-
Coronary artery disease

38
RAB38, member RAS oncogene family
NY-MEL-1, rrGTPbp
Eye neoplasms, Frontotemporal dementia

39
RAB39A, member RAS oncogene family
K28, RAB39
Uterine fibroid

40
RAB39B, member RAS oncogene family
BGMR, MRX72, WSMN, WSN, XLID72
Autism, Chromosome xq28 duplication syndrome, Craniofacial abnormalities, Developmental disability, Early-onset parkinsonism-intellectual disability syndrome, Epilepsy, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability, Parkinsonism with cognitive impairment, Waisman syndrome