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
10771 to 10780 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10771
RAB28, member RAS oncogene family
CORD18
Basal cell carcinoma, Cone dystrophy, Cone-rod dystrophy, Optic atrophy, Retinitis pigmentosa

10772
RAB29, member RAS oncogene family
RAB7L, RAB7L1
Atrial fibrillation, Essential tremor, Hearing loss, Metabolic syndrome, Nephrolithiasis, Parkinson disease, Prostate cancer, Diabetes mellitus type 2

10773
RAB2A, member RAS oncogene family
LHX, RAB2
Autoimmune thyroid disease, Hypothyroidism, Major depressive disorder, Polycystic ovary syndrome, Systemic sclerosis

10774
RAB30, member RAS oncogene family
-
Liver cirrhosis

10775
RAB31, member RAS oncogene family
Rab22B
Alzheimer disease, Bone fracture, Colorectal cancer, Dupuytren contracture, Liver cirrhosis, Lung cancer

10776
RAB32, member RAS oncogene family
PARK26
Allergic contact dermatitis, Differentiated thyroid carcinoma, Leprosy, Liver cirrhosis, Parkinson disease

10777
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

10778
RAB33B, member RAS oncogene family
SMC2
Desbuquois syndrome, Smith-mccort dysplasia

10779
RAB34, member RAS oncogene family
NARR, OFD20, RAB39, RAH
Jeune thoracic dystrophy, Orofaciodigital syndrome

10780
RAB35, member RAS oncogene family
H-ray, RAB1C, RAY
Neurodevelopmental disorder, Non-specific syndromic intellectual disability