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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Hlxtm1Rph/Hlxtm1Rph
FVB.129P2-Hlxtm1Rph
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
Hlxtm1Rph/Hlxtm1Rph
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
Hlxtm1Rph/Hlxtm1Rph
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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last database update
11/12/2019
MGI 6.14
The Jackson Laboratory