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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Egfr+
wild type
MGI:2178395
Summary 18 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
EgfrMhdadsk5/Egfr+ C3HeB/FeJ-EgfrMhdadsk5/Ieg MGI:2682259
ht2
Egfrtm1a(EUCOMM)Wtsi/Egfr+ C57BL/6N-Egfrtm1a(EUCOMM)Wtsi/Wtsi MGI:5781614
ht3
EgfrMhdadsk5/Egfr+ involves: 129S1/SvImJ * C3HeB/FeJ MGI:6403356
ht4
EgfrWa5/Egfr+ involves: BALB/cAnN * C3H/HeN MGI:2686884
ht5
EgfrWa5/Egfr+ involves: BALB/cAnN * C3H/HeN * C57BL/6J MGI:3623311
ht6
EgfrVel/Egfr+ involves: C57BL/6J MGI:3037922
cn7
Chuktm1Yhu/Chuktm1Yhu
Egfrtm1Mag/Egfr+
Tg(KRT5-cre)5132Jlj/0
involves: 129 * C57BL/6 * CD-1 MGI:3817623
cx8
EgfrWa5/Egfr+
Tgfatm1Unc/Tgfatm1Unc
involves: 129P2/OlaHsd * BALB/cAnN * C3H/HeN * C57BL/6J MGI:3623314
cx9
Egfrwa2/Egfr+
Errfi1tm1Kln/Errfi1tm1Kln
involves: 129P2/OlaHsd * C3H/HeSnJ * C57BL/6 MGI:3639757
cx10
Egfrwa2/Egfr+
Fostm2(Fosl1)Wag/Fostm2(Fosl1)Wag
Tg(KRT5-SOS1)892A6Wag/0
involves: 129P2/OlaHsd * C57BL/6 * CBA MGI:5142271
cx11
Egfrwa2/Egfr+
Fostm4.1Wag/Fostm4.1Wag
Tg(KRT5-SOS1)892A6Wag/0
involves: 129P2/OlaHsd * C57BL/6 * CBA MGI:5142272
cx12
Egfrwa2/Egfr+
Fostm3.1Wag/Fostm3.1Wag
Tg(KRT5-SOS1)892A6Wag/0
involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL MGI:5142269
cx13
Egfrwa2/Egfr+
Fostm5.1Wag/Fostm5.1Wag
Tg(KRT5-SOS1)892A6Wag/0
involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL MGI:5142267
cx14
Egfrwa2/Egfr+
Fostm6.1Wag/Fostm6.1Wag
Tg(KRT5-SOS1)892A6Wag/0
involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL MGI:5142268
cx15
Egfrwa2/Egfr+
Nf1tm1Fcr/Nf1+
Trp53tm1Brd/Trp53+
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * C57BL/6JEi * C3H/HeSnJ MGI:5485354
cx16
Egfrwa2/Egfr+
Rps6ka3tm1.1Kry/Y
Tg(KRT5-SOS1)892A6Wag/0
involves: 129X1/SvJ * C57BL/6 * CBA MGI:5142270
cx17
ApcMin/Apc+
EgfrWa5/Egfr+
involves: BALB/cAnN * C3H/HeN * C57BL/6J MGI:3623317
cx18
Egfrwa2/Egfr+
Tg(KRT5-SOS1)892A6Wag/0
involves: C57BL/6 * CBA MGI:5142266


Genotype
MGI:2682259
ht1
Allelic
Composition
EgfrMhdadsk5/Egfr+
Genetic
Background
C3HeB/FeJ-EgfrMhdadsk5/Ieg
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
EgfrMhdadsk5 mutation (0 available); any Egfr mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• excess pigment in a uniform and slanted stripe prominent over the volar pad at the base of the first digit; bluish-gray in color; evident only in adulthood
• pigmentation defects restricted to the footpads

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; evident only in adulthood
• pigmentation defects restricted to the footpads

integument
• slight wave to the coat becomes less apparent with age
• increased nail length seen in some mice
• histologically determined
• excess pigment in a uniform and slanted stripe prominent over the volar pad at the base of the first digit; bluish-gray in color; evident only in adulthood
• pigmentation defects restricted to the footpads




Genotype
MGI:5781614
ht2
Allelic
Composition
Egfrtm1a(EUCOMM)Wtsi/Egfr+
Genetic
Background
C57BL/6N-Egfrtm1a(EUCOMM)Wtsi/Wtsi
Cell Lines EPD0454_5_C09
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrtm1a(EUCOMM)Wtsi mutation (1 available); any Egfr mutation (87 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system

immune system




Genotype
MGI:6403356
ht3
Allelic
Composition
EgfrMhdadsk5/Egfr+
Genetic
Background
involves: 129S1/SvImJ * C3HeB/FeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
EgfrMhdadsk5 mutation (0 available); any Egfr mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• mice infected with a mouse adapted (MA15) version of severe acute respiratory syndrome coronavirus (SARS-CoV) show enhanced lung damage compared to wild-type mice, showing increased perivascular inflammation with interstitial edema, and alveolar and interstitial spaces filled with proteinaceous fluid and inflammatory cells, however they show a similar weight loss, viral titer, and recovery as wild-type control mice
• aged mice (20-24 weeks old) show increased susceptibility to SARS-CoV infection compared to older wild-type mice, showing higher levels of lung damage, increased edema, perivascular cuffing, interstitial inflammation and cuffing around airways, and enhanced cellular proliferation in lungs
• aged mice infected with SARS-CoV show 80% lethality by 5 dpi compared to 30% lethality in wild-type controls

mortality/aging
• aged mice infected with SARS-CoV show 80% lethality by 5 dpi compared to 30% lethality in wild-type controls

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Coronavirus infectious disease DOID:0080599 J:243599




Genotype
MGI:2686884
ht4
Allelic
Composition
EgfrWa5/Egfr+
Genetic
Background
involves: BALB/cAnN * C3H/HeN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
EgfrWa5 mutation (2 available); any Egfr mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• damage from the open eyelids in the form of corneal scarring is dependent on environment, where mice raised in a pathogen free environment have no apparent defects in eye development
• apart from the open eyelids, the eyes of neonates appear normal

integument
• the first coat is described as wavy and subsequent coats are scruffy in appearance




Genotype
MGI:3623311
ht5
Allelic
Composition
EgfrWa5/Egfr+
Genetic
Background
involves: BALB/cAnN * C3H/HeN * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
EgfrWa5 mutation (2 available); any Egfr mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Histological placentae analysis of the EgfrWa5/EgfrWa5 and EgfrWa5/+ mice

embryo
• mildly abnormal placentas
• reduced spongiotrophoblast at E12.5
• variably compromised labyrinthine layer
• multinucleated labyrinthine trophoblasts




Genotype
MGI:3037922
ht6
Allelic
Composition
EgfrVel/Egfr+
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
EgfrVel mutation (1 available); any Egfr mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• the eyes of adult heterozygotes exhibit corneal opacity
• the eyes of adult heterozygotes are often small
• excessive secretions are always observed at the edges of adult heterozygous mutant eyelids, possibly due to infection, drying, or trauma
• migration of eyelid epithelial cells appears to be defective
• at E16.5, the upper and lower eyelids of wild-type embryos are fused in the midline, whereas those of heterozygous mutant embryos remain far apart due to defective migration of eyelid epithelial cells
• heterozygotes are born with eyelids open, whereas the eyelids of wild-type littermates remain closed until 12 days after birth

cellular
• in vitro, mouse embryonic fibroblasts (MEFs) isolated from heterozygous embryos show ~47% reduction in their migratory ability relative to wild-type MEFs

growth/size/body
• significant weight loss is observed with addition of 2% dextran sodium sulfate (DSS) to water, suggesting susceptibility to induced colitis

integument
• coats have a velvet-like texture
• the first coat is wavy
• after the first coat, pelage hair loses its waviness and appears disoriented, with individual shafts projecting in different directions
• heterozygotes are born with curly vibrissae




Genotype
MGI:3817623
cn7
Allelic
Composition
Chuktm1Yhu/Chuktm1Yhu
Egfrtm1Mag/Egfr+
Tg(KRT5-cre)5132Jlj/0
Genetic
Background
involves: 129 * C57BL/6 * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Chuktm1Yhu mutation (0 available); any Chuk mutation (51 available)
Egfrtm1Mag mutation (1 available); any Egfr mutation (87 available)
Tg(KRT5-cre)5132Jlj mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most mice die but some survive
• most mice die but some survive

vision/eye
• mice exhibit eye defects

integument
• mice exhibit hair defects
• slightly




Genotype
MGI:3623314
cx8
Allelic
Composition
EgfrWa5/Egfr+
Tgfatm1Unc/Tgfatm1Unc
Genetic
Background
involves: 129P2/OlaHsd * BALB/cAnN * C3H/HeN * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
EgfrWa5 mutation (2 available); any Egfr mutation (87 available)
Tgfatm1Unc mutation (3 available); any Tgfa mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Phenotypes of Egfrwa2/EgfrWa5 and Tgfatm1Unc/Tgfatm1Unc EgfrWa5/+ mice

growth/size/body
• reduced postnatal growth although size at birth is normal
• noticeably reduced in size by 1 week of age
• 25% reduction in body size in mice surviving to 6 weeks of age

craniofacial
• smaller lower jaw

skeleton
• smaller lower jaw




Genotype
MGI:3639757
cx9
Allelic
Composition
Egfrwa2/Egfr+
Errfi1tm1Kln/Errfi1tm1Kln
Genetic
Background
involves: 129P2/OlaHsd * C3H/HeSnJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Errfi1tm1Kln mutation (0 available); any Errfi1 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• mice display similar epidermal thickening, suprabasal proliferation and impaired differentiation as Errfi1tm1Kln homozygotes




Genotype
MGI:5142271
cx10
Allelic
Composition
Egfrwa2/Egfr+
Fostm2(Fosl1)Wag/Fostm2(Fosl1)Wag
Tg(KRT5-SOS1)892A6Wag/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Fostm2(Fosl1)Wag mutation (0 available); any Fos mutation (43 available)
Tg(KRT5-SOS1)892A6Wag mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• tumor burden is reduced compared to in Tg(KRT5-SOS1)892A6Mka mice

integument




Genotype
MGI:5142272
cx11
Allelic
Composition
Egfrwa2/Egfr+
Fostm4.1Wag/Fostm4.1Wag
Tg(KRT5-SOS1)892A6Wag/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Fostm4.1Wag mutation (0 available); any Fos mutation (43 available)
Tg(KRT5-SOS1)892A6Wag mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• mice exhibit the same tumor burden as Tg(KRT5-SOS1)892A6Mka mice

integument
• mice exhibit the same tumor burden as Tg(KRT5-SOS1)892A6Mka mice




Genotype
MGI:5142269
cx12
Allelic
Composition
Egfrwa2/Egfr+
Fostm3.1Wag/Fostm3.1Wag
Tg(KRT5-SOS1)892A6Wag/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Fostm3.1Wag mutation (0 available); any Fos mutation (43 available)
Tg(KRT5-SOS1)892A6Wag mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• tumor burden is reduced compared to in Tg(KRT5-SOS1)892A6Mka mice

integument




Genotype
MGI:5142267
cx13
Allelic
Composition
Egfrwa2/Egfr+
Fostm5.1Wag/Fostm5.1Wag
Tg(KRT5-SOS1)892A6Wag/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Fostm5.1Wag mutation (0 available); any Fos mutation (43 available)
Tg(KRT5-SOS1)892A6Wag mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• at 4 weeks, tumor volume is decreased 50% compared to in Tg(KRT5-SOS1)892A6Mka mice

integument




Genotype
MGI:5142268
cx14
Allelic
Composition
Egfrwa2/Egfr+
Fostm6.1Wag/Fostm6.1Wag
Tg(KRT5-SOS1)892A6Wag/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Fostm6.1Wag mutation (0 available); any Fos mutation (43 available)
Tg(KRT5-SOS1)892A6Wag mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• papillomas are larger than in Tg(KRT5-SOS1)892A6Mka mice

integument
• papillomas are larger than in Tg(KRT5-SOS1)892A6Mka mice




Genotype
MGI:5485354
cx15
Allelic
Composition
Egfrwa2/Egfr+
Nf1tm1Fcr/Nf1+
Trp53tm1Brd/Trp53+
Genetic
Background
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * C57BL/6JEi * C3H/HeSnJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Nf1tm1Fcr mutation (3 available); any Nf1 mutation (161 available)
Trp53tm1Brd mutation (5 available); any Trp53 mutation (249 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• only 1 of 17 (5.9%) mice develop a tumor, a spindle cell tumor compared to 57.9% of double heterozygous Nf1 and Trp53 mutants; this mouse was sacrificed at 21 weeks of age




Genotype
MGI:5142270
cx16
Allelic
Composition
Egfrwa2/Egfr+
Rps6ka3tm1.1Kry/Y
Tg(KRT5-SOS1)892A6Wag/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Rps6ka3tm1.1Kry mutation (0 available); any Rps6ka3 mutation (13 available)
Tg(KRT5-SOS1)892A6Wag mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• tumor burden is reduced compared to in Tg(KRT5-SOS1)892A6Mka mice

integument




Genotype
MGI:3623317
cx17
Allelic
Composition
ApcMin/Apc+
EgfrWa5/Egfr+
Genetic
Background
involves: BALB/cAnN * C3H/HeN * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ApcMin mutation (12 available); any Apc mutation (156 available)
EgfrWa5 mutation (2 available); any Egfr mutation (87 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• 46% reduction in the number of macroscopic intestinal polyps in comparison to mice heterozygous only for ApcMin at 3 months of age
• no reduction in tumor size




Genotype
MGI:5142266
cx18
Allelic
Composition
Egfrwa2/Egfr+
Tg(KRT5-SOS1)892A6Wag/0
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egfrwa2 mutation (2 available); any Egfr mutation (87 available)
Tg(KRT5-SOS1)892A6Wag mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype




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
03/25/2025
MGI 6.24
The Jackson Laboratory