|
21
|
|
|
B3GALT1 antisense RNA 1 |
- |
|
|
22
|
|
|
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 |
3-Gn-T1, 3-Gn-T2, B3GN-T2, B3GNT, B3GNT-2, B3GNT1, BETA3GNT, BGNT2, BGnT-2, beta-1, beta3Gn-T1, beta3Gn-T2 |
|
|
23
|
|
|
BUB1B-PAK6 readthrough |
PAK-5, PAK-6, PAK5, PAK6 |
|
|
24
|
|
|
Bromodomain containing 8 |
SMAP, SMAP2, p120 |
|
|
25
|
|
|
BTG anti-proliferation factor 3 |
ANA, ANA/BTG3, APRO4, TOB5, TOB55, TOFA |
|
|
26
|
|
|
Beta-1,4-glucuronyltransferase 1 |
B3GN-T1, B3GNT1, B3GNT6, BETA3GNTI, MDDGA13, iGAT, iGNT |
Absence of septum pellucidum, Agenesis of corpus callosum, Alpha-dystroglycanopathy, Anencephaly, Breast cancer, Mammary neoplasms, Breast carcinoma, Cataract, Cerebellar hypoplasia, Cobblestone lissencephaly, Congenital coloboma of iris, Congenital hypoplasia of penis, Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, Cortical dysplasia, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Fukuyama type congenital muscular dystrophy, Glaucoma, Hydrocephalus, Hydronephrosis, Limb-girdle muscular dystrophy, Macrocephaly, Marfan syndrome, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Muscle eye brain disease, Muscular dystrophy, Muscular dystrophy-dystroglycanopathy, Neuronal heterotopia, Occipital encephalocele, Optic atrophy, Pachygyria, Penis agenesis, Polymicrogyria, Posteriorly rotated ear, Retinal detachment, Retinal dysplasia, Retinal dystrophy, Specific learning disorder, Submucosal cleft palate, Syndromic microphthalmia, Walker-warburg congenital muscular dystrophy, Walker-warburg syndromeView all (31 more) |
|
27
|
|
|
Butyrophilin subfamily 3 member A2 |
BT3.2, BTF4, BTN3.2, CD277 |
|
|
28
|
|
|
Butyrophilin subfamily 3 member A1 |
BT3.1, BTF5, BTN3.1, CD277 |
|
|
29
|
|
|
Butyrophilin subfamily 2 member A1 |
BK14H9.1, BT2.1, BTF1, BTN2.1, DJ3E1.1 |
|
|
30
|
|
|
Bromodomain adjacent to zinc finger domain 2A |
TIP5, WALp3 |
|
