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Symbol
Name
ID
Bcor
BCL6 interacting corepressor
MGI:1918708
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Anterior pituitary hypoplasia
Anterior hypopituitarism
Ectopic posterior pituitary
Optic nerve hypoplasia
Spastic paraparesis
Spastic diplegia
Spastic tetraplegia
Delayed CNS myelination
Aplasia/Hypoplasia of the corpus callosum
Agenesis of corpus callosum
Hypoplasia of the corpus callosum
Absent septum pellucidum
Cerebral cortical atrophy
Hypothalamic hamartoma
Cerebellar hypoplasia
Inferior vermis hypoplasia
Colpocephaly
Hydrocephalus
Ventriculomegaly
Aplasia of the optic tract
Absent speech
Intellectual disability, mild
Intellectual disability, progressive
Global developmental delay
Motor delay
Specific learning disability
Seizures
Disease(s) Associated with BCOR
microphthalmia

Mouse Phenotypes
abnormal forebrain development
Availability Mouse Genotype
BcorGt(DB0053)Wtsi/Y
BcorGt(XE541)Byg/Y

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
11/07/2017
MGI 6.11
The Jackson Laboratory