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
10761 to 10770 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10761
RAB19, member RAS oncogene family
RAB19B
Attention deficit hyperactivity disorder, Color vision deficiency, Substance abuse

10762
RAB1A, member RAS oncogene family
RAB1, YPT1
Alzheimer disease, Atrial fibrillation, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Diabetes mellitus type 2

10763
RAB1B, member RAS oncogene family
-
Insomnia, Myocardial ischemia

10764
RAB20, member RAS oncogene family
-
Biliary atresia, Hypothyroidism, Oligodendroglioma

10765
RAB21, member RAS oncogene family
-
Alzheimer disease, Obesity

10766
RAB22A, member RAS oncogene family
-
Cervical cancer

10767
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

10768
RAB25, member RAS oncogene family
CATX-8, RAB11C
Atrial fibrillation, Parkinson disease

10769
RAB27A, member RAS oncogene family
GS2, HsT18676, RAB27, RAM
Autoinflammatory syndrome, Central nervous system cancer, Glioma, Griscelli syndrome, Melanoma, Urinary bladder neoplasms

10770
RAB27B, member RAS oncogene family
C25KG
Anxiety disorder, Asthma, Bipolar disorder, Gestational diabetes, Major depressive disorder, Metabolic syndrome, Mood disorder, Neurotic disorder, Obesity, Oligodendroglioma, Schizophrenia, Diabetes mellitus type 2, Urinary bladder neoplasms, Uveal melanoma