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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rps19Mhdadsk3
Martin Hrabe de Angelis dark skin 3
MGI:2682230
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rps19Mhdadsk3/Rps19Mhdadsk3 involves: C3HeB/FeJ MGI:6260001
hm2
Rps19Mhdadsk3/Rps19Mhdadsk3 involves: C3HeB/FeJ * C57BL/6J MGI:2682231
ht3
Rps19Mhdadsk3/Rps19+ C3HeB/FeJ-Rps19Mhdadsk3/Ieg MGI:2682232
cx4
Rps19Mhdadsk3/Rps19+
Trp53tm1Tyj/Trp53+
involves: 129S2/SvPas * C3HeB/FeJ MGI:6260014
cx5
Rps19Mhdadsk3/Rps19+
Tg(Dct-lacZ)A12Jkn/0
involves: C3HeB/FeJ * C57BL/6 * CBA MGI:6259996
cx6
KitW-v/Kit+
Rps19Mhdadsk3/Rps19+
involves: C3HeB/FeJ * C57BL/6J MGI:6260000


Genotype
MGI:6260001
hm1
Allelic
Composition
Rps19Mhdadsk3/Rps19Mhdadsk3
Genetic
Background
involves: C3HeB/FeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rps19Mhdadsk3 mutation (0 available); any Rps19 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:2682231
hm2
Allelic
Composition
Rps19Mhdadsk3/Rps19Mhdadsk3
Genetic
Background
involves: C3HeB/FeJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rps19Mhdadsk3 mutation (0 available); any Rps19 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:2682232
ht3
Allelic
Composition
Rps19Mhdadsk3/Rps19+
Genetic
Background
C3HeB/FeJ-Rps19Mhdadsk3/Ieg
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rps19Mhdadsk3 mutation (0 available); any Rps19 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• ~10% of adult mice exhibit a white belly spot
• increased ear pigmentation is seen by 3 weeks of age and persists throughout adult life
• adults show excess epidermal pigmentation in the footpads, tail and ears
• excess pigment in a uniform and slanted stripe prominent over the volar pad at the base of the first digit; bluish-gray in color (J:86685)
• increased footpad pigmentation is seen by 3 weeks of age and persists throughout adult life; pigment accumulates in the footpad epidermis (J:139244)
• at P3, P10 and P30, Kitl (kit ligand) mRNA levels are significantly increased in the footpad epidermis relative to control mice (J:139244)
• increased Trp53 staining is noted in the adult footpad epidermis relative to control mice (J:139244)
• dark pigmentation of the tail (J:81301)
• increased tail pigmentation is seen by 3 weeks of age and persists throughout adult life (J:139244)
• pigment accumulates in the adult tail epidermis, whereas the dermis is unaffected (J:139244)

integument
• ~10% of adult mice exhibit a white belly spot
• increased ear pigmentation is seen by 3 weeks of age and persists throughout adult life
• adults show excess epidermal pigmentation in the footpads, tail and ears
• excess pigment in a uniform and slanted stripe prominent over the volar pad at the base of the first digit; bluish-gray in color (J:86685)
• increased footpad pigmentation is seen by 3 weeks of age and persists throughout adult life; pigment accumulates in the footpad epidermis (J:139244)
• at P3, P10 and P30, Kitl (kit ligand) mRNA levels are significantly increased in the footpad epidermis relative to control mice (J:139244)
• increased Trp53 staining is noted in the adult footpad epidermis relative to control mice (J:139244)
• dark pigmentation of the tail (J:81301)
• increased tail pigmentation is seen by 3 weeks of age and persists throughout adult life (J:139244)
• pigment accumulates in the adult tail epidermis, whereas the dermis is unaffected (J:139244)

growth/size/body
• increased ear pigmentation is seen by 3 weeks of age and persists throughout adult life
• mice show a ~10-15% reduction in birth weight relative to control mice
• at P21, mice exhibit a significant reduction in body weight on both an inbred (C3HeB/HeJ) and a mixed genetic background

hematopoietic system
• mice exhibit a lower red blood cell (RBC) count on both an inbred (C3HeB/HeJ) and a mixed genetic background
• ~5% and ~10% reductions in RBC count are noted at 8 weeks and 20 weeks of age, respectively
• mice show a ~50% reduction in reticulocyte count relative to control mice

cellular
• at 8 weeks of age, mice exhibit an increase in annexin V-positive bone marrow progenitor cells (lineage-cKit+) relative to control mice, indicating increased apoptosis
• however, bone marrow cytology is normal

limbs/digits/tail
• excess pigment in a uniform and slanted stripe prominent over the volar pad at the base of the first digit; bluish-gray in color (J:86685)
• increased footpad pigmentation is seen by 3 weeks of age and persists throughout adult life; pigment accumulates in the footpad epidermis (J:139244)
• at P3, P10 and P30, Kitl (kit ligand) mRNA levels are significantly increased in the footpad epidermis relative to control mice (J:139244)
• increased Trp53 staining is noted in the adult footpad epidermis relative to control mice (J:139244)
• dark pigmentation of the tail (J:81301)
• increased tail pigmentation is seen by 3 weeks of age and persists throughout adult life (J:139244)
• pigment accumulates in the adult tail epidermis, whereas the dermis is unaffected (J:139244)

craniofacial
• increased ear pigmentation is seen by 3 weeks of age and persists throughout adult life

hearing/vestibular/ear
• increased ear pigmentation is seen by 3 weeks of age and persists throughout adult life




Genotype
MGI:6260014
cx4
Allelic
Composition
Rps19Mhdadsk3/Rps19+
Trp53tm1Tyj/Trp53+
Genetic
Background
involves: 129S2/SvPas * C3HeB/FeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rps19Mhdadsk3 mutation (0 available); any Rps19 mutation (25 available)
Trp53tm1Tyj mutation (12 available); any Trp53 mutation (232 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
N
• adult mice exhibit reversal of the hyperpigmentation phenotype seen in the footpad and tail skin of single Rps19Mhdadsk3 heterozygotes

growth/size/body
N
• adult mice exhibit reversal of the body weight phenotypes seen in single Rps19Mhdadsk3 heterozygotes

hematopoietic system
• adult mice exhibit reversal of the erythrocyte phenotype seen in single Rps19Mhdadsk3 heterozygotes




Genotype
MGI:6259996
cx5
Allelic
Composition
Rps19Mhdadsk3/Rps19+
Tg(Dct-lacZ)A12Jkn/0
Genetic
Background
involves: C3HeB/FeJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rps19Mhdadsk3 mutation (0 available); any Rps19 mutation (25 available)
Tg(Dct-lacZ)A12Jkn mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• an increased number of Xgal+ cells (melanocytes) are first detected in the basal layer of the footpad epidermis at P3 and persist in the adult footpad, indicating postnatal epidermal melanocytosis
• an increased number of Xgal+ cells (melanocytes) are first detected in the basal layer of the footpad epidermis at P3 and persist in the adult footpad

integument
• an increased number of Xgal+ cells (melanocytes) are first detected in the basal layer of the footpad epidermis at P3 and persist in the adult footpad, indicating postnatal epidermal melanocytosis

embryo
• a decreased number of Xgal+ cells (melanoblasts) is observed at E15.5 and other embryonic time points
• a ventral surface area devoid of Xgal+ cells is observed at E15.5

nervous system
• a decreased number of Xgal+ cells (melanoblasts) is observed at E15.5 and other embryonic time points
• a ventral surface area devoid of Xgal+ cells is observed at E15.5




Genotype
MGI:6260000
cx6
Allelic
Composition
KitW-v/Kit+
Rps19Mhdadsk3/Rps19+
Genetic
Background
involves: C3HeB/FeJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
KitW-v mutation (10 available); any Kit mutation (179 available)
Rps19Mhdadsk3 mutation (0 available); any Rps19 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• adult mice show a larger white belly spot than mice that are only heterozygous for the KitW-v allele

integument
• adult mice show a larger white belly spot than mice that are only heterozygous for the KitW-v allele





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory