chromosome 1q21.1 deletion syndrome

Summary
Synonym
  • 1q21.1 microdeletion syndrome
Definition
A chromosomal deletion syndrome that has_material_basis_in a contiguous deletion of the 1q21.1 region on chromosome 1 and is characterized by an increases the risk of delayed development, intellectual disability, physical abnormalities, and neurological and psychiatric problems.
Super Class
chromosomal deletion syndrome
Disease Ontology
DOID:0060411
Mondo Disease Ontology
ORDO
OMIM
GARD
WikiPathways (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
607 BCL9 BCL9 transcription coactivator
283149 BCL9L BCL9 like
Displaying all 2 entries
Gene ID Gene Symbol Description Source
77578 Bcl9 B cell CLL/lymphoma 9
80288 Bcl9l B cell CLL/lymphoma 9-like

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024