Glmn Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Glmn
glomulin, FKBP associated protein
MGI:2141180

31 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Glmn^em1(IMPC)Bay/Glmn^em1(IMPC)Bay C57BL/6N-Glmn^em1(IMPC)Bay/BayMmucd	abnormal chorioallantoic fusion	J:211773
	abnormal embryo development	J:211773
	abnormal embryo size	J:211773
	abnormal embryo turning	J:211773
	abnormal forebrain development	J:211773
	abnormal heart looping	J:211773
	abnormal heart morphology	J:211773
	abnormal hindbrain development	J:211773
	abnormal midbrain development	J:211773
	abnormal neural tube closure	J:211773
	abnormal neural tube morphology	J:211773
	abnormal pharyngeal arch morphology	J:211773
	abnormal somite shape	J:211773
	abnormal tail bud morphology	J:211773
	abnormal visceral yolk sac morphology	J:211773
	abnormal vitelline vasculature morphology	J:211773
	bleb	J:211773
	embryonic growth retardation	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	hemorrhage	J:211773
	pale yolk sac	J:211773
	pallor	J:211773
	preweaning lethality, complete penetrance	J:211773
Glmn^{Gt(OST109778)Lex}/Glmn^{Gt(OST109778)Lex} involves: 129S5/SvEvBrd * C57BL/6	abnormal head mesenchyme morphology	J:184206
	delayed neural tube closure	J:184206
	disorganized yolk sac vascular plexus	J:184206
	embryonic growth retardation	J:184206
	embryonic lethality during organogenesis, complete penetrance	J:184206
	hemorrhage	J:184206
	incomplete embryo turning	J:184206
	increased apoptosis	J:184206
	pericardial effusion	J:184206
Glmn^m1Btlr/Glmn^m1Btlr C57BL/6J-Glmn^m1Btlr/Btlr	increased bone mineral density	J:309727

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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