About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Grhl3
grainyhead like transcription factor 3
MGI:2655333
61 phenotypes from 9 alleles in 17 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Grhl3ct-2J/Grhl3ct-2J
C57BL/6J-Grhl3ct-2J/J
abnormal neural tube morphology J:87349
curly tail J:87349
Grhl3ct-J/Grhl3ct-J
STOCK T(7;15)9H
curly tail J:87487
open neural tube J:87487
Grhl3ct/Grhl3+
involves: C57BL/6 * GFF
curly tail J:24376
Grhl3ct/Grhl3ct-J
Not Specified
curly tail J:87487
open neural tube J:87487
Grhl3ct/Grhl3ct
GFF-Grhl3ct
abnormal neural tube closure J:1549, J:6246
curly tail J:6864
exencephaly J:6245, J:6864
fetal growth retardation J:6864
spina bifida J:6864
Grhl3ct/Grhl3ct
involves: CBA/Gr * GFF
abnormal dorsal-ventral axis patterning J:79
anencephaly J:264
curly tail J:264
delayed neural tube closure J:79
spina bifida J:264
Grhl3ct/Grhl3ct
involves: GFF
abnormal neural tube closure J:14716
curly tail J:14716
spina bifida J:14716
Grhl3ct/Grhl3ct
STOCK Grhl3ct/J
curly tail J:86772
exencephaly J:86772
spina bifida cystica J:86772
Grhl3ct/Grhl3ct
Tg(Grhl3)1Ndeg/0
involves: GFF
normal nervous system phenotype J:129979
Grhl3ct/Grhl3tm1Jane
involves: 129S1/Sv * C57BL/6 * STOCK ct/J
spina bifida J:86772
Grhl3tm1(cre)Cgh/Grhl3tm1(cre)Cgh
involves: 129P2/OlaHsd * C57BL/6 * SJL
abnormal brain development J:157446
abnormal neural tube morphology J:157446
exencephaly J:157446
spina bifida J:157446
Grhl3tm1a(EUCOMM)Wtsi/Grhl3+
C57BL/6N-Grhl3tm1a(EUCOMM)Wtsi/Ics
abnormal eye morphology J:165965
abnormal locomotor activation J:165965
abnormal retina morphology J:165965
decreased blood urea nitrogen level J:165965
decreased circulating alkaline phosphatase level J:165965
decreased circulating triglyceride level J:165965
decreased IgE level J:165965
increased circulating calcium level J:165965
increased circulating glucose level J:165965
Grhl3tm1Bogi/Grhl3+
involves: C57BL/6J
abnormal craniofacial development J:226218
abnormal periderm development J:226218
Grhl3tm1Bogi/Grhl3tm1Bogi
involves: C57BL/6 * C57BL/6J
abnormal palate development J:226218
abnormal periderm development J:226218
cleft palate J:226218
Grhl3tm1Bogi/Grhl3tm1Bogi
involves: C57BL/6J
abnormal corneocyte morphology J:114626
abnormal epidermal layer morphology J:114626
abnormal epidermis stratum basale morphology J:114626
abnormal epidermis stratum corneum morphology J:114626
abnormal epidermis stratum granulosum morphology J:114626
abnormal intestine morphology J:114626
abnormal keratinocyte differentiation J:114626
abnormal lipid level J:114626
abnormal neural tube closure J:114626
abnormal stomach epithelium morphology J:114626
curly tail J:114626
epidermal hyperplasia J:114626
exencephaly J:114626
eyelids open at birth J:114626
impaired skin barrier function J:114626
increased keratinocyte proliferation J:114626
intestinal hemorrhage J:114626
perinatal lethality, complete penetrance J:114626
spina bifida J:114626
thick epidermis J:114626
thick epidermis stratum spinosum J:114626
Grhl3tm1Jane/Grhl3+
involves: 129S1/Sv
normal neoplasm J:178952
Grhl3tm1Jane/Grhl3tm1Jane
involves: 129S1/Sv
abnormal vertebral pedicle morphology J:164805
increased keratinocyte proliferation J:178952
spina bifida J:164805
thick epidermis J:178952
Grhl3tm1Jane/Grhl3tm1Jane
involves: 129S1/Sv * C57BL/6
abnormal corneocyte envelope morphology J:233531
abnormal vertebrae morphology J:86772
abnormal vertebral spinous process morphology J:86772
absent vertebral arch J:86772
decreased embryo size J:86772
exencephaly J:86772
kinked tail J:86772
kyphosis J:86772
preweaning lethality, complete penetrance J:86772
spina bifida J:86772
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(KRT14-cre)8Brn/0
involves: 129S1/Sv * C57BL/6 * FVB/N
epidermal hyperplasia J:178952
increased incidence of tumors by chemical induction J:178952
increased skin papilloma incidence J:178952
increased skin squamous cell carcinoma incidence J:178952
normal integument phenotype J:178952, J:233531
Grhl3tm1Jane/Grhl3tm3.1Jane
Tg(MMTV-cre)4Mam/0
involves: 129S1/Sv * C57BL/6 * FVB
abnormal skin morphology J:178952
abnormal skin physiology J:178952
increased tumor incidence J:178952
Grhl3tm3.1Jane/Grhl3tm3.1Jane
involves: 129S1/Sv * C57BL/6
no abnormal phenotype detected J:178952

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
11/19/2024
MGI 6.24
The Jackson Laboratory