About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Hsf1
heat shock factor 1
MGI:96238
33 phenotypes from 5 alleles in 8 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Hsf1tm1.1(KOMP)Vlcg/Hsf1+
C57BL/6N-Hsf1tm1.1(KOMP)Vlcg/J
abnormal retina morphology J:211773
abnormal sleep behavior J:211773
decreased circulating glucose level J:211773
Hsf1tm1.1(KOMP)Vlcg/Hsf1tm1.1(KOMP)Vlcg
C57BL/6N-Hsf1tm1.1(KOMP)Vlcg/J
abnormal embryo size J:211773
preweaning lethality, incomplete penetrance J:211773
Hsf1tm1.1Echr/Hsf1tm1.1Echr
Tg(Zp3-cre)93Knw/0
involves: 129S2/SvPas * C57BL/6J
abnormal female meiosis J:175085
abnormal meiotic spindle assembly checkpoint J:175085
Hsf1tm1Anak/Hsf1tm1Anak
involves: C57BL/6 * CBA * ICR
abnormal spermatogenesis J:89846
normal reproductive system phenotype J:89846
Hsf1tm1Anak/Hsf1tm1Anak
involves: ICR
normal vision/eye phenotype J:93301
Hsf1tm1Ijb/Hsf1tm1Ijb
129.129S6-Hsf1tm1Ijb
abnormal astrocyte morphology J:93600
abnormal brain morphology J:93600
abnormal brain ventricle morphology J:93600
abnormal brain white matter morphology J:93600
abnormal corpus callosum morphology J:93600
abnormal putamen morphology J:93600
abnormal striatum morphology J:93600
dilated lateral ventricle J:93600
dilated third ventricle J:93600
Hsf1tm1Ijb/Hsf1tm1Ijb
either: (involves: 129S6/SvEvTac * 129X1/SvJ) or (involves: 129S6/SvEvTac * BALB/c) or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * ICR)
abnormal extraembryonic tissue morphology J:58383
abnormal placenta labyrinth morphology J:58383
decreased body weight J:58383
decreased spongiotrophoblast size J:58383
failure of zygotic cell division J:65267
female infertility J:58383, J:65267
increased susceptibility to bacterial infection J:58383
increased tumor necrosis factor secretion J:58383
postnatal growth retardation J:58383
prenatal lethality, incomplete penetrance J:58383, J:73593
Hsf1tm1Ijb/Hsf1tm1Ijb
involves: 129S6/SvEvTac
abnormal chromosomal synapsis J:175085
abnormal female meiosis J:175085
abnormal meiotic spindle assembly checkpoint J:175085
abnormal synaptonemal complex J:175085
Hsf1tm1Miv/Hsf1tm1Miv
involves: 129S2/SvPas * C57BL/6
abnormal cell death J:88534
decreased sensitivity to induced cell death J:88534
female infertility J:88534

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory