|
51
|
|
|
WD repeat domain 35 |
CED2, CFAP118, FAP118, IFT121, IFTA1, SRTD7 |
Acrocephaly, Agenesis of corpus callosum, Ambiguous genitalia, Anodontia, Asphyxiating thoracic dystrophy, Biliary cirrhosis, Blepharophimosis, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Cerebellar hypoplasia, Cholangitis, Cholestasis, Ciliopathies, Clinodactyly, Brain malformation, Congenital duplication of uterus, Congenital epicanthus, Congenital hepatic fibrosis, Pulmonary hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Congenital pectus excavatum, Cranioectodermal dysplasia, Craniosynostosis, Cryptorchidism, Cutis laxa, Dandy-walker syndrome, Dolichocephaly, Dwarfism, Ectodermal dysplasia, Ectopic anus, Esophageal atresia, Frontal bossing, High palate, Hydronephrosis, Hydrops fetalis, Hyperbilirubinemia, Hypertension, Hypodontia, Hypospadias, Imperforate anus, Jeune thoracic dystrophy, Left ventricular hypertrophy, Liver fibrosis, Cystic hygroma, Macrocephaly, Majewski syndrome, Mesomelia, Metopic synostosis, Microdontia, Micrognathism, Micromelia, Myopia, Nail diseases, Nail dysplasia, Nystagmus, Osteoporosis, Patent ductus arteriosus, Patent foramen ovale, Plagiocephaly, Polycystic kidney disease, Polydactyly, Polysplenia, Renal cyst, Renal hypoplasia, Renal insufficiency, Rhizomelia, Scaphocephaly, Short rib-polydactyly syndrome, Short-rib thoracic dysplasia without polydactyly, Syndactyly, Syndactyly of fingers, Synostotic anterior plagiocephaly, Synostotic posterior plagiocephaly, Taurodontism, Thoracic dysplasia, Trigonocephaly, Postaxial hand polydactylyView all (65 more) |
|
52
|
|
|
WD repeat domain 48 |
Bun62, P80, SPG60, UAF1 |
|
|
53
|
|
|
WDFY family member 4 |
C10orf64 |
|
|
54
|
|
|
WD repeat domain 19 |
ATD5, CED4, CFAP66, DYF-2, FAP66, IFT144, NPHP13, ORF26, Oseg6, PWDMP, SPGF72, SRTD5 |
Anetoderma, Brachydactyly, Camptodactyly of fingers, Caroli disease, Cataract, Ciliopathies, Congenital epicanthus, Congenital hepatic fibrosis, Congenital pectus excavatum, Cranioectodermal dysplasia, Craniosynostosis, Cutis laxa, Developmental delay, Diastrophic dysplasia, Dolichocephaly, Dwarfism, Ectodermal dysplasia, Foot polydactyly, Frontal bossing, Glomerulonephritis, Hyperopia, Hypertension, Hypodontia, Interstitial nephritis, Jeune syndrome, Jeune thoracic dystrophy, Keratosis follicularis, Kidney disease, Liver cyst, Microdontia, Micromelia, Myopia, Nephronophthisis, Nystagmus, Osteochondrodysplasia, Osteoporosis, Pancreatic cyst, Premature menopause, Renal dysplasia and retinal aplasia, Renal hypoplasia, Renal insufficiency, Retinal dystrophy, Rhizomelia, Rod-cone dystrophy, Senior-loken syndrome, Short rib-polydactyly syndrome, Skeletal dysplasia, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Taurodontism, Thoracic dysplasia, Thoracic hypoplasia, Postaxial hand polydactylyView all (39 more) |
|
55
|
|
|
WAP four-disulfide core domain 1 |
PS20 |
|
|
56
|
|
|
WNK lysine deficient protein kinase 1 |
HSAN2, HSN2, KDP, PPP1R167, PRKWNK1, PSK, p65 |
Acrosteolysis, Anhidrosis, Breast cancer, Colorectal cancer, Dysautonomia, Gastroesophageal reflux disease, Hereditary sensory and autonomic neuropathy, Hyperchloremia, Hyperpotassemia and hypertension, Hypertension, Kidney disease, Lung carcinoma, Lung adenocarcinoma, Nervous system diseases, Neuropathy, Paronychia inflammation, PseudohypoaldosteronismView all (2 more) |
|
57
|
|
|
WNK lysine deficient protein kinase 4 |
PHA2B, PRKWNK4 |
Hyperchloremia, Hyperpotassemia and hypertension, Hypertension, Metastatic melanoma, Ovarian adenocarcinoma, Pseudohypoaldosteronism, Sex reversal, female, with dysgenesis of kidneys, adrenals, and lungs |
|
58
|
|
|
WNK lysine deficient protein kinase 3 |
MRXS2, PRKWNK3, PRS |
|
|
59
|
|
|
WNK lysine deficient protein kinase 2 |
NY-CO-43, P/OKcl.13, PRKWNK2, SDCCAG43 |
|
|
60
|
|
|
Tryptophanyl-tRNA synthetase 1 |
GAMMA-2, HMN9, HMND9, IFI53, IFP53, NEDMSBA, WARS |
|
