11
|
|
|
WD repeat domain 17 |
- |
|
12
|
|
|
WASP homolog associated with actin, golgi membranes and microtubules |
WHAMM1, WHDC1 |
|
13
|
|
|
WD repeat domain 81 |
CAMRQ2, CHMRQ, HYC3, PPP1R166, SORF-2 |
Brain atrophy, Cataract, Cerebellar ataxia, mental retardation, and dysequilibrium syndrome, Cerebellar atrophy, Cerebellar hypoplasia, Cerebral atrophy, Cerebral palsy, Congenital anomaly of neck, Congenital hydrocephalus, Congenital hydrocephalus, with brain anomalies, Dandy-walker syndrome, Developmental delay, Dwarfism, Dysarthria, Dysequilibrium syndrome, Holoprosencephaly, Hydranencephaly, Hydrocephalus, Hypoplasia of corpus callosum, Mental retardation, Macrocephaly, StrabismusView all (7 more) |
14
|
|
|
WD repeat domain 88 |
PQWD |
|
15
|
|
|
WD repeat domain 36 |
GLC1G, TA-WDRP, TAWDRP, UTP21 |
|
16
|
|
|
WW domain binding protein 2 pseudogene 1 |
- |
|
17
|
|
|
WD repeat domain 49 |
CFAP337 |
|
18
|
|
|
WD repeat domain 37 |
NOCGUS |
Anterior segment dysgenesis, Cardiovascular abnormalities, Cerebellar hypoplasia, Congenital ocular coloboma, Developmental delay, Dysmorphism, Epilepsy, Kidney disease, Kidney failure, Mental retardation, Microcornea, Urogenital abnormalities |
19
|
|
|
WD repeat and FYVE domain containing 3 |
ALFY, BCHS, MCPH18, ZFYVE25 |
|
20
|
|
|
WAPL cohesin release factor |
FOE, KIAA0261, WAPAL |
|