|
91
|
|
|
KAT8 regulatory NSL complex subunit 1 |
C17DELq21.31, CENP-36, DEL17Q21.31, KDVS, KIAA1267, MSL1v1, NSL1, hMSL1v1 |
17 deletion, 17q21.31 deletion syndrome, Adenocarcinoma, Alopecia, male pattern, Androgenetic alopecia, Anxiety disorder, Arachnodactyly, Atrial septal defect, Bicuspid aortic valve, Blepharophimosis, Breast carcinoma, Congenital epicanthus, Contiguous gene syndrome, Cryptorchidism, Development disorder, Developmental delay, Dysmorphic features, Dysphagia, Eczema, High palate, Hydronephrosis, Hyperopia, Hypoplasia of corpus callosum, Mental retardation, Koolen-de vries syndrome, Laryngomalacia, Leukemia, megakaryoblastic, of down syndrome, Lung diseases, Macrotia, Mental depression, Mood disorder, Multicystic renal dysplasia, Multiple congenital anomalies, Hypotonia, Neuronal heterotopia, Ovarian neoplasm, Ovarian cancer, Parkinson disease, Patent ductus arteriosus, Biliary cirrhosis, Ptosis, Pulmonary stenosis, Scoliosis, Strabismus, Ventricular septal defect, Vesicoureteral refluxView all (31 more) |
|
92
|
|
|
Keratin 18 pseudogene 55 |
- |
|
|
93
|
|
|
Potassium channel tetramerization domain containing 1 |
C18orf5 |
Anodontia, Aplasia cutis congenita, Breast carcinoma, Cataract, Breast aplasia, Diabetes mellitus, Double ureter, Hypertension, Hypohidrosis, Microtia, Nail diseases, Nail dysplasia, Pyelonephritis, Scalp-ear-nipple syndrome, Syndactyly of fingers, Syndactyly of the toesView all (1 more) |
|
94
|
|
|
KIF9 antisense RNA 1 |
- |
|
|
95
|
|
|
KIAA0825 |
C5orf36, PAPA10 |
|
|
96
|
|
|
Keratin 6C |
K6E, KRT6E, PPKNEFD |
|
|
97
|
|
|
KLF transcription factor 15 |
KKLF |
|
|
98
|
|
|
Potassium voltage-gated channel interacting protein 3 |
CSEN, DREAM, KCHIP3 |
|
|
99
|
|
|
Potassium voltage-gated channel interacting protein 1 |
KCHIP1, VABP |
|
|
100
|
|
|
Kelch like family member 10 |
SPGF11 |
|
