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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Tlx1
T cell leukemia, homeobox 1
MGI:98769
10 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Tlx1tm1.1(cre/ERT2)Rygo/Tlx1tm1.1(cre/ERT2)Rygo
involves: C57BL/6 * C57BL/6JJcl * C57BL/6NSlc
absent spleen J:217489
Tlx1tm1Sjk/Tlx1tm1Sjk
involves: 129S2/SvPas
abnormal spleen development J:17695
abnormal spleen mesenchyme morphology J:17695
absent spleen J:17695
normal embryo phenotype J:17695
increased leukocyte cell number J:17695
increased lymphocyte cell number J:17695
increased neutrophil cell number J:17695
increased number of Howell-Jolly bodies J:17695
normal nervous system phenotype J:17695
Tlx1tm1Thr/Tlx1tm1Thr
involves: 129P2/OlaHsd * MF1
abnormal spleen development J:28700
absent spleen J:28700
increased splenocyte apoptosis J:28700

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
03/24/2020
MGI 6.15
The Jackson Laboratory