Brd1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Brd1
bromodomain containing 1
MGI:1924161

18 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Brd1^tm1Hko/Brd1^tm1Hko B6.129-Brd1^tm1Hko	abnormal embryonic erythropoiesis	J:177092
	abnormal embryonic hematopoiesis	J:177092
	abnormal erythropoiesis	J:177092
	abnormal fetal liver hematopoietic progenitor cell morphology	J:177092
	abnormal lens morphology	J:177092
	abnormal optic cup morphology	J:177092
	anemia	J:177092
	decreased erythroblast number	J:177092
	decreased erythroid progenitor cell number	J:177092
	decreased hepatoblast number	J:177092
	embryonic growth retardation	J:177092
	embryonic lethality during organogenesis, incomplete penetrance	J:177092
	impaired hematopoiesis	J:177092
	increased apoptosis	J:177092
	lethality throughout fetal growth and development, complete penetrance	J:177092
	open neural tube	J:177092
	pallor	J:177092
	small liver	J:177092

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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