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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Krt75tm1Der
targeted mutation 1, Dennis R Roop
MGI:3762626
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Krt75tm1Der/Krt75tm1Der involves: 129S6/SvEvTac * C57BL/6J MGI:3762631
ht2
Krt75tm1Der/Krt75+ involves: 129S6/SvEvTac * C57BL/6J MGI:3762630
cx3
Krt6a/Krt6btm1Der/Krt6b+
Krt75tm1Der/Krt75+
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J MGI:3762628
cx4
Krt6a/Krt6btm1Der/Krt6a+
Krt75tm1Der/Krt75+
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J MGI:3762629


Genotype
MGI:3762631
hm1
Allelic
Composition
Krt75tm1Der/Krt75tm1Der
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt75tm1Der mutation (0 available); any Krt75 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• by 2 weeks of age mice exhibit rough coats that is not localized to any anatomical structure and persists throughout life
• sulfur levels within focal swellings is decreased (1.24+/-0.40% compared to 1.98+/-0.40% in wild-type shafts)
• in some regions the cuticle splits and eventually breaks exposing the rounded ghost cells
• heavily pigmented and mildly to non-pigmented hair shafts have defects ranging from loose irregular aggregation of pigment, clumping of pigment within the medulla, clumping with focal distention of the shaft, segregation of pigment with a light brown colored medullary abnormality, to breaking of the hair in the middle of these deformities
• hair shafts display blebs comprising 7.88+/-2.27% of counted hair shafts
• focal distentions are associated with clusters of looses aggregates of round cells associated with fracturing of the cuticle, leading to breakage of the shaft
• all four pelage hair types including vibrissae are affected by hair defects
• nails on hindfeet, most frequently, in males thicken distally and are often lost
• nail plates are opaque with a rough surface and are overgrown laterally and vertically
• some nail beds are separated from the overlying connective tissue and contain large hemorrhagic areas
• while some hair follicles appear normal others have focal swellings in the precortical region of the anagen VI-stage follicles immediately above the dermal papilla that contain eosinophilic cells with basophilic nuclei
• vibrissae contain irregularly spaced bulges with clumping pigment




Genotype
MGI:3762630
ht2
Allelic
Composition
Krt75tm1Der/Krt75+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt75tm1Der mutation (0 available); any Krt75 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• by 2 weeks of age mice exhibit rough coats although less prominently than in homozygotes
• hair shafts display blebs comprising 3.02+/-0.52% of counted hair shafts




Genotype
MGI:3762628
cx3
Allelic
Composition
Krt6a/Krt6btm1Der/Krt6b+
Krt75tm1Der/Krt75+
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt6a/Krt6btm1Der mutation (0 available); any Krt6b mutation (24 available)
Krt75tm1Der mutation (0 available); any Krt75 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• authors state that the phenotypes observed are no more severe than those in Krt75tm1Der heterozygotes
• authors state that the phenotypes observed are no more severe than those in Krt75tm1Der heterozygotes




Genotype
MGI:3762629
cx4
Allelic
Composition
Krt6a/Krt6btm1Der/Krt6a+
Krt75tm1Der/Krt75+
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt6a/Krt6btm1Der mutation (0 available); any Krt6a mutation (25 available)
Krt75tm1Der mutation (0 available); any Krt75 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• authors state that the phenotypes observed are no more severe than those in Krt75tm1Der heterozygotes
• authors state that the phenotypes observed are no more severe than those in Krt75tm1Der heterozygotes





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory