|
291
|
|
|
Zinc finger FYVE-type containing 16 |
PPP1R69 |
|
|
292
|
|
|
Zinc finger protein 623 |
- |
|
|
293
|
|
|
Zinc finger E-box binding homeobox 2 |
HSPC082, SIP-1, SIP1, SMADIP1, ZFHX1B |
Accessory nipple, Nonmedullary thyroid carcinoma, Atrial septal defect, Bilateral arterial duct, Breast cancer, Mammary neoplasms, Breast carcinoma, Cataract, Cerebellar diseases, Colorectal cancer, Congenital anomaly of eye, Asplenia, Congenital coloboma of iris, Congenital heart defects, Congenital pectus carinatum, Congenital pectus excavatum, Coronary artery disease, Dysmorphic features, Esotropia, Fundus coloboma, Hirschsprung disease, Hydronephrosis, Hypoplasia of corpus callosum, Mental retardation, Interrupted inferior vena cava with azygous continuation, Marden-walker syndrome, Marfan syndrome, Microcephaly, Microcornea, Microphthalmos, Motor delay, Motor disorders, Mowat-wilson syndrome, Muckle-wells syndrome, Multiple congenital anomalies, Myopia, Papillary thyroid carcinoma, Patent ductus arteriosus, Ptosis, Pulmonary stenosis, Renal carcinoma, Retinal coloboma, Schizophrenia, Strabismus, Subaortic stenosis, Submucosal cleft palate, Thyroid cancer, Ventricular septal defectView all (33 more) |
|
294
|
|
|
Zinc finger and BTB domain containing 24 |
BIF1, ICF2, PATZ2, ZNF450 |
Anemia, Communicating hydrocephalus, Congenital epicanthus, Congenital exomphalos, Developmental delay, Dwarfism, Bronchitis, High palate, Immunodeficiency-centromeric instability-facial anomalies syndrome, Immunologic deficiency syndromes, Lymphopenia, Macrocephaly, Macroglossia, Malabsorption syndrome, Mental retardation, Micrognathism, Motor delayView all (2 more) |
|
295
|
|
|
Zinc finger CCCH-type containing 11A |
ZC3HDC11A |
|
|
296
|
|
|
Zinc finger and BTB domain containing 39 |
ZNF922 |
|
|
297
|
|
|
Zinc finger BED-type containing 4 |
- |
|
|
298
|
|
|
Zinc finger and BTB domain containing 40 |
ZNF923 |
|
