Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10741 to 10750 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10741
RAB3A interacting protein
RABIN3, RABIN8
Atrial fibrillation, Color vision deficiency

10742
RAB40A like
MRXSMP, RAR2, RLGP
Cognition disorder, Craniofacial abnormalities, Growth disorder, Partington syndrome, X-linked intellectual disability

10743
RAB40B, member RAS oncogene family
RAR, SEC4L
Oligodendroglioma, Skin disease, Diabetes mellitus type 2

10744
RAB40C, member RAS oncogene family
RARL, RASL8C
Alzheimer disease, Insomnia, Major salivary gland carcinoma

10745
RAB42, member RAS oncogene family
-
Autism

10746
RAB44, member RAS oncogene family
RASD3, RASL13, dJ431A14.3
Systemic lupus erythematosus, Uterine fibroid

10747
RAB4B, member RAS oncogene family
-
Obstructive pulmonary disease, Prostatic neoplasms

10748
RAB5A, member RAS oncogene family
RAB5
Myocardial ischemia, Schizophrenia

10749
RAB5B, member RAS oncogene family
-
Anorexia nervosa, Asthma, Eczema, Autoimmune disease, Basal cell carcinoma, Gastroesophageal reflux disease, Hashimoto disease, Hypothyroidism, Nasal polyp, Peptic ulcer disease, Polycystic ovary syndrome, Psoriasis, Rheumatoid arthritis, Diabetes mellitus type 1, Diabetes mellitus type 2
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10750
RAB5C, member RAS oncogene family
L1880, RAB5CL, RAB5L, RABL
Autoimmune disease, Autoimmune thyroid disease, Coronary artery disease, Hypothyroidism, Intellectual developmental disorder, Vitiligo