|
Symbol Name ID |
Ctcf
CCCTC-binding factor MGI:109447 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spastic gait |
Ventriculomegaly |
Thin corpus callosum |
Periventricular leukomalacia |
Cerebral atrophy |
Cerebellar atrophy |
Arachnoid cyst |
Ataxia |
Depression |
Aggressive behavior |
Attention deficit hyperactivity disorder |
Delayed speech and language development |
Anxiety |
Autistic behavior |
Compulsive behaviors |
Motor stereotypy |
Intellectual disability |
Sleep abnormality |
Dystonia |
Global developmental delay |
Delayed ability to walk |
Bilateral tonic-clonic seizure with generalized onset |
Generalized tonic seizure |
| Disease(s) Associated with CTCF | ||||||||||||||||||||||||
| autosomal dominant intellectual developmental disorder 21 |
| Mouse Phenotypes | abnormal neurite morphology |
abnormal nervous system electrophysiology |
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| Availability | Mouse Genotype | ||
| Ctcfem1Hyao/Ctcfem1Hyao | |||
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 03/25/2025 MGI 6.24 |
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