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
10801 to 10810 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10801
RAB6A, member RAS oncogene family
RAB6
Alzheimer disease, Insomnia, Obesity

10802
RAB7A, member RAS oncogene family
CMT2B, PRO2706, RAB7
Alzheimer disease, Attention deficit hyperactivity disorder, Charcot-marie-tooth disease, Hereditary motor and sensory neuropathies, Myocardial ischemia, Substance abuse

10803
RAB7B, member RAS oncogene family
RAB7
Cystic fibrosis, Diabetes mellitus, Lewy body disease, Osteoporosis, Diabetes mellitus type 2

10804
RAB8A, member RAS oncogene family
MEL, RAB8
Rheumatoid arthritis

10805
RAB8B, member RAS oncogene family
-
Dental caries, Liver cirrhosis, Schizophrenia

10806
RAB9B, member RAS oncogene family
RAB9L, Rab-9L
Auditory neuropathy, Intellectual developmental disorder, Pelizaeus-merzbacher disease, Spastic paraplegia, x-linked, Hereditary spastic paraplegia

10807
Rabaptin, RAB GTPase binding effector protein 1
RAB5EP, RABPT5
Alzheimer disease, Metabolic syndrome, Rheumatoid arthritis, Diabetes mellitus type 2

10808
Rabaptin, RAB GTPase binding effector protein 2
FRA
Brody myopathy, Glomerulonephritis, Obesity, Parkinson disease, Diabetes mellitus type 2

10809
Rab9 effector protein with kelch motifs
RAB9P40, bA65N13.1, p40
Anxiety disorder, Cannabis abuse, Myopia

10810
RAB GTPase activating protein 1
GAPCENA, TBC1D11
Astrocytoma, Central nervous system cancer, Kidney disease, Neurodevelopmental disorder, Glioma, Insomnia, Kidney failure, Non-specific syndromic intellectual disability, Osteoarthritis, Diabetes mellitus type 2