Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "R"
41 to 50 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

41
RAB3D, member RAS oncogene family
D2-2, GOV, RAB16, RAD3D
Alzheimer disease

42
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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43
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

44
RAB3A interacting protein like 1
GRAB
Migraine, Schizophrenia

45
RAB3A interacting protein
RABIN3, RABIN8
Atrial fibrillation, Color vision deficiency

46
RAB40A like
MRXSMP, RAR2, RLGP
Cognition disorder, Craniofacial abnormalities, Growth disorder, Partington syndrome, X-linked intellectual disability

47
RAB40B, member RAS oncogene family
RAR, SEC4L
Oligodendroglioma, Skin disease, Diabetes mellitus type 2

48
RAB40C, member RAS oncogene family
RARL, RASL8C
Alzheimer disease, Insomnia, Major salivary gland carcinoma

49
RAB42, member RAS oncogene family
-
Autism

50
RAB44, member RAS oncogene family
RASD3, RASL13, dJ431A14.3
Systemic lupus erythematosus, Uterine fibroid