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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Patz1
POZ (BTB) and AT hook containing zinc finger 1
MGI:1891832
43 phenotypes from 4 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Patz1tm1.1(KOMP)Vlcg/Patz1tm1.1(KOMP)Vlcg
C57BL/6N-Patz1tm1.1(KOMP)Vlcg/Ucd
preweaning lethality, complete penetrance J:211773
Patz1tm1.1Welm/Patz1tm1.1Welm
involves: 129P2/OlaHsd
abnormal T cell subpopulation ratio J:158947
decreased body size J:158947
decreased body weight J:158947
decreased splenocyte number J:158947
decreased thymocyte number J:158947
prenatal lethality, incomplete penetrance J:158947
Patz1tm1.1Welm/Patz1tm1.1Welm
involves: 129P2/OlaHsd * C57BL/6
prenatal lethality J:158947
Patz1tm1.2Welm/Patz1tm1.2Welm
involves: 129P2/OlaHsd
no abnormal phenotype detected J:209168
Patz1tm1.2Welm/Patz1tm1.2Welm
Commd10Tg(Vav1-icre)A2Kio/Commd10+
B6.Cg-Patz1tm1.2Welm Commd10Tg(Vav1-icre)A2Kio
abnormal mast cell differentiation J:209168
decreased interleukin-6 secretion J:209168
normal immune system phenotype J:209168
Patz1tm1.2Welm/Patz1tm1.2Welm
Tg(Cma1-cre)#Roer/0
involves: 129P2/OlaHsd * C57BL/6
normal immune system phenotype J:209168
Patz1tm1Pchi/Patz1+
involves: C57BL/6J
increased fibroblast proliferation J:190572
Patz1tm1Pchi/Patz1tm1Pchi
involves: C57BL/6J
abnormal brain morphology J:190572
abnormal cardiac outflow tract development J:190572
abnormal cell cycle J:190572
abnormal choroid plexus morphology J:190572
abnormal descending aorta morphology J:190572
abnormal diencephalon morphology J:190572
abnormal embryonic neuroepithelium morphology J:190572
abnormal embryonic/fetal subventricular zone morphology J:190572
abnormal hindbrain morphology J:190572
decreased body size J:190572
decreased body weight J:190572
decreased brain size J:190572
decreased fetal size J:190572
decreased fibroblast proliferation J:190572
early cellular replicative senescence J:190572
embryonic lethality during organogenesis, incomplete penetrance J:190572
enlarged brain ventricles J:190572
exencephaly J:190572
incomplete rostral neuropore closure J:190572
lethality throughout fetal growth and development, incomplete penetrance J:190572
postnatal growth retardation J:190572
transposition of great arteries J:190572
Patz1tm1Pchi/Patz1tm1Pchi
Not Specified
abnormal seminiferous tubule morphology J:133515
abnormal spermatogonia proliferation J:133515
arrest of spermatogenesis J:133515
azoospermia J:133515
decreased testis weight J:133515
female infertility J:133515
increased Leydig cell number J:133515
male infertility J:133515
small seminiferous tubules J:133515
small testis J:133515

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
11/12/2024
MGI 6.24
The Jackson Laboratory