|
161
|
|
|
Ubiquitin specific peptidase 32 |
NY-REN-60, USP10 |
|
|
162
|
|
|
UTP4 small subunit processome component |
CIRH1A, CIRHIN, NAIC, TEX292 |
|
|
163
|
|
|
Ubiquitin associated and SH3 domain containing B |
STS-1, STS1, TULA-2, TULA2, p70 |
|
|
164
|
|
|
Ubiquitin specific peptidase 45 |
LCA19 |
|
|
165
|
|
|
USO1 vesicle transport factor |
P115, TAP, VDP |
|
|
166
|
|
|
Unc-5 netrin receptor C |
UNC5H3 |
|
|
167
|
|
|
URI1 prefoldin like chaperone |
C19orf2, NNX3, PPP1R19, RMP, URI |
|
|
168
|
|
|
Ubiquitin specific peptidase 13 |
ISOT3, IsoT-3 |
|
|
169
|
|
|
Ubiquitin protein ligase E3B |
BPIDS, KOS |
Absent eyebrow, Aortic coarctation, Arachnodactyly, Astigmatism, Atrial septal defect, Blepharophimosis, Brachycephaly, Congenital alveolar dysplasia, Camptodactyly of fingers, Chorioretinal dystrophy, Choroideremia, Developmental dysplasia of the hip, Congenital epicanthus, Congenital malrotation of intestine, Developmental delay, Dwarfism, Dysmorphic features, Hypertrophy of clitoris, Hypocholesterolemia, Hypoplasia of corpus callosum, Mental retardation, Kaufman oculocerebrofacial syndrome, Laryngomalacia, Laryngospasm, Macrostomia, Microcephaly, Microcornea, Microdontia, Micrognathism, Microstomia, Motor delay, Multiple congenital anomalies, Myopia, Nystagmus, Optic atrophy, Polydactyly, Ptosis, Respiratory failure, Specific learning disorder, Strabismus, Ventricular septal defectView all (26 more) |
|
170
|
|
|
Ubiquitin protein ligase E3D |
C6orf157, H10BH, UBE2CBP, YJR141W |
|
