All Phenotypes St14<Gt(RST485)Byg> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

St14^{Gt(RST485)Byg}
gene trap RST485, BayGenomics
MGI:3717153

Summary

2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	St14^{Gt(RST485)Byg}/St14^{Gt(RST485)Byg}	involves: 129P2/OlaHsd * Black Swiss	MGI:3717472
ht2	St14^{Gt(RST485)Byg}/St14⁺	involves: 129P2/OlaHsd * Black Swiss	MGI:3717473

Allelic Composition	St14^{Gt(RST485)Byg}/St14^{Gt(RST485)Byg}
Genetic Background	involves: 129P2/OlaHsd * Black Swiss

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
St14^{Gt(RST485)Byg} mutation (0 available); any St14 mutation (44 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

digestive/alimentary system

abnormal hard palate morphology ( J:108567 )

• the keratinized epithelium of the tongue and hard palate has increased permeability as measured by a dye absorption assay

abnormal tongue epithelium morphology ( J:108567 )

• the keratinized epithelium of the tongue and hard palate has increased permeability as measured by a dye absorption assay

craniofacial

abnormal hard palate morphology ( J:108567 )

• the keratinized epithelium of the tongue and hard palate has increased permeability as measured by a dye absorption assay

abnormal tongue epithelium morphology ( J:108567 )

• the keratinized epithelium of the tongue and hard palate has increased permeability as measured by a dye absorption assay

growth/size/body

abnormal hard palate morphology ( J:108567 )

• the keratinized epithelium of the tongue and hard palate has increased permeability as measured by a dye absorption assay

abnormal tongue epithelium morphology ( J:108567 )

• the keratinized epithelium of the tongue and hard palate has increased permeability as measured by a dye absorption assay

Allelic Composition	St14^{Gt(RST485)Byg}/St14⁺
Genetic Background	involves: 129P2/OlaHsd * Black Swiss

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
St14^{Gt(RST485)Byg} mutation (0 available); any St14 mutation (44 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

homeostasis/metabolism

impaired skin barrier function ( J:108567 )

• at E14.5 and E15.5, mice have reduced epithelial barrier function as measured by a dye assay

integument

impaired skin barrier function ( J:108567 )

• at E14.5 and E15.5, mice have reduced epithelial barrier function as measured by a dye assay

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