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
10711 to 10720 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10711
RAB17, member RAS oncogene family
-
Atrial fibrillation, Obesity, Scoliosis

10712
RAB18, member RAS oncogene family
RAB18LI1, WARBM3
Apert syndrome, Asthma, Congenital malformation syndromes predominantly affecting facial appearance, Cryptophthalmos syndrome, Cyclocephaly, Epilepsy, Goldenhar syndrome, Mobius syndrome, Orofaciodigital syndrome, Rolandic epilepsy, Scoliosis, Warburg micro syndrome

10713
RAB19, member RAS oncogene family
RAB19B
Attention deficit hyperactivity disorder, Color vision deficiency, Substance abuse

10714
RAB1A, member RAS oncogene family
RAB1, YPT1
Alzheimer disease, Atrial fibrillation, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Diabetes mellitus type 2

10715
RAB1B, member RAS oncogene family
-
Insomnia, Myocardial ischemia

10716
RAB20, member RAS oncogene family
-
Biliary atresia, Hypothyroidism, Oligodendroglioma

10717
RAB21, member RAS oncogene family
-
Alzheimer disease, Obesity

10718
RAB22A, member RAS oncogene family
-
Cervical cancer

10719
RAB23, member RAS oncogene family
HSPC137
Alzheimer disease, Bladder exstrophy and epispadias complex, Carpenter syndrome, Coronary artery disease, Desbuquois syndrome, Gastrointestinal stromal tumor, Myocardial infarction, Myocardial ischemia, Systemic lupus erythematosus

10720
RAB25, member RAS oncogene family
CATX-8, RAB11C
Atrial fibrillation, Parkinson disease