41
|
|
|
RAB3C, member RAS oncogene family |
- |
|
42
|
|
|
RAB3D, member RAS oncogene family |
D2-2, GOV, RAB16, RAD3D |
|
43
|
|
|
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, Intellectual disability, Uranostaphyloschisis, Warburg micro syndromeView all (3 more) |
44
|
|
|
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 |
45
|
|
|
RAB3A interacting protein like 1 |
GRAB |
|
46
|
|
|
RAB3A interacting protein |
RABIN3, RABIN8 |
|
47
|
|
|
RAB40A like |
MRXSMP, RAR2, RLGP |
|
48
|
|
|
RAB40B, member RAS oncogene family |
RAR, SEC4L |
|
49
|
|
|
RAB40C, member RAS oncogene family |
RARL, RASL8C |
|
50
|
|
|
RAB42, member RAS oncogene family |
- |
|