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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Krt1
keratin 1
MGI:96698
21 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Krt1Mhdadsk12/Krt1+
C3HeB/FeJ-Krt1Mhdadsk12
abnormal skin pigmentation J:108758
acanthosis J:108758
blistering J:108758
hyperkeratosis J:108758
hyperpigmentation J:108758
scaly skin J:108758
Krt1Mhdadsk12/Krt1Mhdadsk12
C3HeB/FeJ-Krt1Mhdadsk12
blistering J:108758
dehydration J:108758
epidermal desquamation J:108758
postnatal lethality, complete penetrance J:108758
Krt1tm1Tmm/Krt1tm1Tmm
involves: 129 * C57BL/6
abnormal blood cell morphology/development J:200244
abnormal cerebellar granule layer morphology J:200244
abnormal circulating interleukin level J:200244
abnormal corneocyte envelope morphology J:200244
abnormal interleukin secretion J:200244
abnormal skin morphology J:200244
abnormal vasculogenesis J:200244
impaired skin barrier function J:200244
increased circulating interleukin-18 level J:200244
increased vascular permeability J:200244
neonatal lethality, incomplete penetrance J:200244
weight loss J:200244

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
04/16/2024
MGI 6.23
The Jackson Laboratory