Hlx Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Hlx
H2.0-like homeobox
MGI:96109

19 phenotypes from 1 allele in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Hlx^tm1Rph/Hlx^tm1Rph FVB.129P2-Hlx^tm1Rph	abnormal enteric neuron morphology	J:119681
	abnormal liver development	J:119681
	decreased circulating serum albumin level	J:119681
	decreased fetal size	J:119681
	hydrops fetalis	J:119681
	pallor	J:119681
	perinatal lethality, complete penetrance	J:119681
Hlx^tm1Rph/Hlx^tm1Rph involves: 129P2/OlaHsd	abnormal diaphragm morphology	J:31553
	abnormal erythropoiesis	J:31553
	abnormal intestine morphology	J:31553
	abnormal liver bud morphology	J:31553
	abnormal liver development	J:31553
	absent gallbladder	J:31553
	anemia	J:31553
	diaphragmatic hernia	J:31553
	enlarged lung	J:31553
	impaired hematopoiesis	J:31553
	liver hypoplasia	J:31553
	prenatal lethality, complete penetrance	J:31553
	small pancreas	J:31553
Hlx^tm1Rph/Hlx^tm1Rph Tg(DBHn-lacZ)8Rpk/0 involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	abnormal enteric neuron morphology	J:119681

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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