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CRRD ID: 1317578
Species: Mus musculus
CRRD Object: Gene
Symbol: Trp53bp1
Name: transformation related protein 53 binding protein 1
Acc ID: DOID:0080107
Term: microcephaly and chorioretinopathy 3
Definition: A syndrome that is characterized by congenital microcephaly and chorioretinal dysplasia associated with poor vision and nystagmus and has_material_basis_in compound heterozygous mutation in the TUBGCP4 gene. (DO)
Definition Source(s):
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
QualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
 ISORGD:13175778554872ClinVarClinVar Annotator: match by term: Microcephaly and chorioretinopathy, autosomal recessive, 3

PMID:24033266, PMID:25741868, PMID:25817018
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.