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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Fraser extracellular matrix complex subunit 1
51 phenotypes from 5 alleles in 8 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
abnormal digit morphology J:175213
abnormal eye morphology J:175213
absent kidney J:175213
micrognathia J:175213
perimembraneous ventricular septal defect J:175213
involves: C3H/HeH * C57BL/6JAnu
absent kidney J:199856
bleb J:199856
cleft secondary palate J:199856
eyelids open at birth J:199856
preaxial polydactyly J:199856
involves: C57BL/6JAnu
abnormal palatal shelf fusion at midline J:208682
abnormal rib morphology J:208682
abnormal secondary palate development J:208682
abnormal sternebra morphology J:208682
abnormal sternum morphology J:208682
absent kidney J:208682
bleb J:208682
blistering J:208682
cleft secondary palate J:208682
normal craniofacial phenotype J:208682
hemorrhage J:208682
narrow eye opening J:208682
preaxial polydactyly J:208682
small kidney J:208682
involves: 101/H * C3H/HeH
abnormal basement membrane morphology J:83745
abnormal hair growth J:13501
abnormal kidney development J:83745
abnormal metanephric mesenchyme morphology J:83745
abnormal metanephros morphology J:83745
abnormal ureteric bud morphology J:83745
absent kidney J:13501, J:83745
bleb J:13501
clubfoot J:13501, J:83745
cryptophthalmos J:83745
delayed kidney development J:83745
fetal bleb J:83745
impaired branching involved in ureteric bud morphogenesis J:83745
increased metanephric mesenchyme apoptosis J:83745
kidney cysts J:83745
microphthalmia J:13501
prenatal lethality, incomplete penetrance J:83745
single kidney J:13501, J:83745
small kidney J:83745
syndactyly J:83745
involves: 101/H * C3H/HeH * C57BL/6 * FVB/N * SJL
abnormal glomerular capillary morphology J:190659
abnormal glomerular capsule space morphology J:190659
abnormal glomerular mesangium morphology J:190659
abnormal renal glomerulus morphology J:190659
cortical renal glomerulopathies J:190659
glomerulosclerosis J:190659
normal integument phenotype J:190659
normal renal/urinary system phenotype J:190659
involves: C57BL/6 * FVB/N * SJL
absent kidney J:190659
blistering J:190659
hemorrhage J:190659
involves: 129S1/Sv * 129X1/SvJ * C57BL/10
absent kidney J:83746
blistering J:83746
cryptophthalmos J:83746
lethality throughout fetal growth and development, complete penetrance J:83746
lethality throughout fetal growth and development, incomplete penetrance J:83746
syndactyly J:83746
involves: 129S1/Sv * 129X1/SvJ * NMRI
abnormal basement membrane morphology J:137010
abnormal lung development J:137010
abnormal lung epithelium morphology J:137010
abnormal lung morphology J:137010
abnormal lung vasculature morphology J:137010
fused right lung lobes J:137010

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
MGI 6.14
The Jackson Laboratory