Symbol Name ID |
Pogz
pogo transposable element with ZNF domain MGI:2442117 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Hypoglycemic seizures |
Optic nerve hypoplasia |
Abnormality of visual evoked potentials |
Delayed CNS myelination |
Thin corpus callosum |
Hypoplasia of the corpus callosum |
Cerebral atrophy |
Delayed speech and language development |
Irritability |
Anxiety |
Overfriendliness |
Autistic behavior |
Aggressive behavior |
Tics |
Hyperactivity |
Motor stereotypy |
Self-injurious behavior |
Intellectual disability |
Sleep abnormality |
Obstructive sleep apnea |
Waddling gait |
Global developmental delay |
Motor delay |
Focal impaired awareness seizure |
Disease(s) Associated with POGZ | |||||||||||||||||||||||||
White-Sutton syndrome |
Mouse Phenotypes | decreased brain weight |
decreased forebrain size |
decreased brain size |
abnormal somatosensory cortex morphology |
increased dendritic spine density |
increased excitatory postsynaptic current frequency |
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Availability | Mouse Genotype | ||||||
Pogzem1Tnkw/Pogz+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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