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
10791 to 10800 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10791
RAB40A like
MRXSMP, RAR2, RLGP
Cognition disorder, Craniofacial abnormalities, Growth disorder, Partington syndrome, X-linked intellectual disability

10792
RAB40B, member RAS oncogene family
RAR, SEC4L
Liver cirrhosis, Oligodendroglioma, Skin disease, Diabetes mellitus type 2

10793
RAB40C, member RAS oncogene family
RARL, RASL8C
Alzheimer disease, Insomnia, Major salivary gland carcinoma

10794
RAB42, member RAS oncogene family
-
Autism

10795
RAB44, member RAS oncogene family
RASD3, RASL13, dJ431A14.3
Systemic lupus erythematosus, Uterine fibroid

10796
RAB4B, member RAS oncogene family
-
Obstructive pulmonary disease, Prostatic neoplasms

10797
RAB5A, member RAS oncogene family
RAB5
Myocardial ischemia, Schizophrenia

10798
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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10799
RAB5C, member RAS oncogene family
L1880, RAB5CL, RAB5L, RABL
Autoimmune disease, Autoimmune thyroid disease, Coronary artery disease, Hypothyroidism, Intellectual developmental disorder, Vitiligo

10800
RAB5 interacting factor
C20orf24, CFSMR2, OPTI, PNAS-11, RCAF1, RIP5
Breast cancer, Cancer, Cleft palate and bilateral cleft lip, Colorectal cancer, Congenital fusion of ribs, Craniofacial dysmorphism skeletal anomalies intellectual disability syndrome, Estrogen-receptor negative breast cancer, Intellectual developmental disorder, Lung cancer, Melanoma, Micrognathism, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Scoliosis
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