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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Klf4
Kruppel-like transcription factor 4 (gut)
MGI:1342287
64 phenotypes from 4 alleles in 8 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Klf4em1(IMPC)Kmpc/Klf4em1(IMPC)Kmpc
C57BL/6NTac-Klf4em1(IMPC)Kmpc/Kmpc
decreased grip strength J:211773
Klf4tm1.1Khk/Klf4tm1.1Khk
involves: 129S6/SvEvTac * C57BL/6
abnormal colon goblet cell morphology J:76493
abnormal intestinal epithelium morphology J:76493
neonatal lethality, complete penetrance J:76493
Klf4tm1Efu/Klf4tm1Efu
Not Specified
abnormal epidermis stratum corneum morphology J:56495
abnormal epidermis stratum granulosum morphology J:56495
abnormal suckling behavior J:56495
abnormal tongue epithelium morphology J:56495
dehydration J:56495
impaired skin barrier function J:56495
neonatal lethality, complete penetrance J:56495
parakeratosis J:56495
Klf4tm1Khk/Klf4tm1Khk
involves: 129S6/SvEvTac * C57BL/6
no abnormal phenotype detected J:76493
Klf4tm1Khk/Klf4tm1Khk
Lyz2tm1(cre)Ifo/0
involves: 129P2/OlaHsd * 129S6/SvEvTac
decreased Ly6C low monocyte number J:239509
Klf4tm1Khk/Klf4tm1Khk
Plekha5Tg(AMH-cre)1Flor/Plekha5+
involves: C57BL/6 * SJL
abnormal seminiferous tubule epithelium morphology J:132612
abnormal seminiferous tubule size J:132612
abnormal Sertoli cell development J:132612
abnormal testes secretion J:132612
decreased circulating testosterone level J:132612
normal reproductive system phenotype J:132612
Klf4tm1Khk/Klf4tm1Khk
Tg(ED-L2-cre)267Jkat/0
involves: 129S6/SvEvTac * C57BL/6
abnormal esophageal epithelium morphology J:161868
abnormal keratinocyte differentiation J:161868
abnormal keratinocyte morphology J:161868
abnormal skin morphology J:161868
abnormal tongue squamous epithelium morphology J:161868
focal ventral hair loss J:161868
skin lesions J:161868
Klf4tm1Khk/Klf4tm1Khk
Tg(Foxa3-cre)1Khk/0
involves: 129S6/SvEvTac * C57BL/6 * DBA
abnormal gastric chief cell morphology J:97350
abnormal gastric gland morphology J:97350
abnormal gastric parietal cell morphology J:97350
abnormal gastric surface mucous cell morphology J:97350
abnormal mucous neck cell morphology J:97350
abnormal stomach epithelium morphology J:97350
abnormal stomach mucosa morphology J:97350
gastric hypertrophy J:97350
preneoplasia J:97350
Klf4tm1Khk/Klf4tm1Khk
Tg(Klf4-cre/ERT)1Wai/0
involves: 129S6/SvEvTac * C57BL/6 * CBA
abnormal intestinal epithelium morphology J:188101
abnormal intestinal goblet cell morphology J:188101
ectopic Paneth cells J:188101
impaired wound healing J:187932
increased hair follicle cell proliferation J:187932
increased hair follicle number J:189337
increased incidence of tumors by chemical induction J:189337
increased keratinocyte adhesion J:189337
increased keratinocyte migration J:189337
increased keratinocyte proliferation J:187932, J:189337
increased Paneth cell number J:188101
thick epidermis suprabasal layer J:189337
Klf4tm1Khk/Klf4tm1Khk
Tg(Pax6-cre,GFP)1Pgr/0
involves: 129S6/SvEvTac * FVB/N
abnormal Bowman membrane morphology J:117671
abnormal cornea anterior stroma morphology J:117671
abnormal cornea endothelium morphology J:117671
abnormal cornea epithelium morphology J:117671
abnormal cornea stroma morphology J:117671
abnormal eye morphology J:117671
abnormal lens fiber morphology J:117671
absent conjunctiva goblet cells J:117671
acoria J:117671
blepharitis J:117671
decreased cornea epithelium thickness J:117671
increased cornea fragility J:117671
increased cornea stroma thickness J:117671
iris hyperplasia J:117671
lens vacuoles J:117671
microphthalmia J:117671
small lens J:117671
small pupil J:117671

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