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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Hba-x
hemoglobin X, alpha-like embryonic chain in Hba complex
MGI:96019
13 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Hba-xtm1Led/Hba-x+
involves: 129S6/SvEvTac * NIH Black Swiss
abnormal hemoglobin J:41934
abnormal mean corpuscular hemoglobin J:41934
abnormal mean corpuscular volume J:41934
Hba-xtm1Led/Hba-xtm1Led
involves: 129S6/SvEvTac
prenatal lethality, complete penetrance J:41934
Hba-xtm1Led/Hba-xtm1Led
involves: 129S6/SvEvTac * NIH Black Swiss
abnormal erythrocyte morphology J:41934
abnormal hemoglobin J:41934
abnormal mean corpuscular hemoglobin J:41934
abnormal mean corpuscular volume J:41934
anemia J:41934
anisocytosis J:41934
decreased litter size J:41934
poikilocytosis J:41934
polychromatophilia J:41934
postnatal growth retardation J:41934
prenatal lethality, incomplete penetrance J:41934
thrombocytosis J:41934

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
04/23/2024
MGI 6.23
The Jackson Laboratory