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
10751 to 10760 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10751
RAB11A, member RAS oncogene family
YL8
Astrocytoma, Nonsyndromic intellectual disability, Chloracne, Congenital microcephaly, Intellectual disability, Neurodevelopmental disorder

10752
RAB11B, member RAS oncogene family
H-YPT3, NDAGSCW
Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus type 2

10753
RAB11 family interacting protein 2
Rab11-FIP2, nRip11
Asthma, Basal cell carcinoma, Celiac disease, Choroidal melanoma, Colorectal cancer, Melanoma, Diverticulitis, Gout, Retinopathy, Squamous cell carcinoma, Diabetes mellitus type 2

10754
RAB11 family interacting protein 4
FIP4-Rab11, RAB11-FIP4
Keratoconus, Metabolic syndrome, Prostate cancer, Diabetes mellitus type 2

10755
RAB11 family interacting protein 5
GAF1, RIP11, gaf-1, pp75, rab11-FIP5
Autism, Schizophrenia

10756
RAB12, member RAS oncogene family
-
Eczema, Colorectal cancer, Inflammatory skin disease, Myocardial ischemia, Oligodendroglioma, Psoriasis, Scoliosis, Hypertension

10757
RAB13, member RAS oncogene family
GIG4
Prostate cancer

10758
RAB14, member RAS oncogene family
FBP, RAB-14
Neurodevelopmental disorder

10759
RAB17, member RAS oncogene family
-
Atrial fibrillation, Obesity, Scoliosis

10760
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