11
|
|
|
ZNF816-ZNF321P readthrough |
ZNF816-ZNF321 |
|
12
|
|
|
ZNF433 and ZNF878 antisense RNA 1 |
- |
|
13
|
|
|
Zinc metallopeptidase STE24 |
FACE-1, FACE1, HGPS, PRO1, RSDM1, STE24, Ste24p |
Acanthosis nigricans, Acquired kyphoscoliosis, Acrosteolysis, Adrenal hypoplasia, x-linked, Alopecia, Arthritis, Arthrogryposis multiplex congenita, Atrial septal defect, Blepharophimosis, Carotid artery stenosis, Choanal atresia, Clinodactyly, Congenital anomaly of neck, Short clavicles, Pulmonary hypoplasia, Congenital kyphoscoliosis, Congenital microcephaly, Defect of skull ossification, Dextrocardia, Double ureter, Dwarfism, Entropion, Fatty liver, Glomerular hyalinosis, Glomerulosclerosis, Hearing loss, High palate, Hutchinson-gilford syndrome, Hydropic placenta, Hyperglycemia, Hyperinsulinism, Hyperlipidemia, Hyperopia, Hyperphosphatemia, Hypertension, Hypodontia, Hypogonadotropic hypogonadism, Hypohidrosis, Hypoplasia of nipple, Hypoplasia of teeth, Hypospadias, Hypotrichosis, Insulin-resistant diabetes mellitus, Keratoconjunctivitis sicca, Left ventricular hypertrophy, Lethal tight skin contracture syndrome, Lipoatrophy, Lipodystrophy, Macrocephaly, Macrotia, Mandibular diseases, Mandibuloacral dysplasia with lipodystrophy, Maternal hypertension, Microcolon, Micrognathism, Microstomia, Microtia, Nail diseases, Nail dysplasia, Nail dystrophy, Neck webbing, Hypoglycemia, Osteopenia, Osteoporosis, Patent ductus arteriosus, Progeria, Proptosis, Restrictive dermopathy, Sinus tachycardia, Skin erosion, Submucosal cleft palate, Temporomandibular ankylosis, Thrombocytosis, Transient ischemic attack, Transposition of great vessels, Vertical talusView all (61 more) |
14
|
|
|
ZFPM2 antisense RNA 1 |
SCAT3 |
|
15
|
|
|
Zinc finger protein 267 |
HZF2 |
|
16
|
|
|
Zinc finger HIT-type containing 1 |
CG1I, ZNFN4A1, p18(Hamlet) |
|
17
|
|
|
Zinc finger and BTB domain containing 18 |
C1DELq42q44, C1DELq43q44, C2H2-171, DEL1Q42Q44, DEL1Q43Q44, MRD22, RP58, TAZ-1, ZNF238 |
Agenesis of corpus callosum, Congenital epicanthus, Developmental delay, Distal monosomy 1q, Dwarfism, Dysmorphic features, Mental retardation, Microcephaly, Micrognathism, Movement disorders, Multiple congenital anomalies |
18
|
|
|
Zinc finger MYND-type containing 11 |
BRAM1, BS69, MRD30 |
|
19
|
|
|
Zinc finger protein 268 |
HZF3 |
|
20
|
|
|
ZW10 interacting kinetochore protein |
HZwint-1, KNTC2AP, SIP30, ZWINT1 |
|