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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
Aplasia/Hypoplasia of the corpus callosum
Abnormality of speech or vocalization
Self-injurious behavior
Intellectual disability
Intellectual disability, mild
Global developmental delay
Seizure
Disease(s) Associated with BCOR
syndromic microphthalmia 1
syndromic microphthalmia 2

Mouse Phenotypes
abnormal forebrain development
decreased forebrain size
Availability Mouse Genotype
BcorGt(DB0053)Wtsi/Y
BcorGt(XE541)Byg/Y
Bcortm1.1Vjba/Y
Tmem163Tg(ACTB-cre)2Mrt/Tmem163+  (conditional)

Contributing Projects:
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
06/04/2024
MGI 6.13
The Jackson Laboratory