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
10781 to 10790 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10781
RAB37, member RAS oncogene family
-
Coronary artery disease

10782
RAB38, member RAS oncogene family
NY-MEL-1, rrGTPbp
Eye neoplasms, Frontotemporal dementia

10783
RAB39A, member RAS oncogene family
K28, RAB39
Uterine fibroid

10784
RAB39B, member RAS oncogene family
BGMR, MRX72, WSMN, WSN, XLID72
Autism, Chromosome xq28 duplication syndrome, Craniofacial abnormalities, Developmental disability, Early-onset parkinsonism-intellectual disability syndrome, Epilepsy, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability, Parkinsonism with cognitive impairment, Waisman syndrome

10785
RAB3C, member RAS oncogene family
-
Breast cancer, Central nervous system infection, Major depressive disorder, Diabetes mellitus type 2

10786
RAB3D, member RAS oncogene family
D2-2, GOV, RAB16, RAD3D
Alzheimer disease

10787
RAB3 GTPase activating protein catalytic subunit 1
MARTS2, P130, RAB3GAP, RAB3GAP130, WARBM1
Apert syndrome, Bilateral microphthalmos, Cataract-intellectual disability-hypogonadism syndrome, Congenital cataract, Congenital malformation syndromes predominantly affecting facial appearance, Congenital ptosis, Cryptophthalmos syndrome, Cryptorchidism, Cyclocephaly, Goldenhar syndrome, Hypertrichosis, Martsolf syndrome, Mobius syndrome, Movement disorder, Orofaciodigital syndrome
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10788
RAB3 GTPase activating non-catalytic protein subunit 2
MARTS1, RAB3-GAP150, RAB3GAP150, SPG69, WARBM2, p150
Apert syndrome, Attention deficit hyperactivity disorder, Spastic paraplegia, Cataract-intellectual disability-hypogonadism syndrome, Congenital cataract, Congenital malformation syndromes predominantly affecting facial appearance, Cryptophthalmos syndrome, Cyclocephaly, Goldenhar syndrome, Martsolf syndrome, Microphthalmos, Mobius syndrome, Orofaciodigital syndrome, Substance abuse, Warburg micro syndrome

10789
RAB3A interacting protein like 1
GRAB
Migraine, Schizophrenia

10790
RAB3A interacting protein
RABIN3, RABIN8
Atrial fibrillation, Color vision deficiency