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Symbol
Name
ID
Fbn1
fibrillin 1
MGI:95489
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Abnormal abdomen morphology
Hepatomegaly
Protuberant abdomen
Incisional hernia
Umbilical hernia
Reduced upper to lower segment ratio
Short stature
Proportionate short stature
Severe short stature
Tall stature
Disproportionate tall stature
Disease(s) Associated with FBN1
acromicric dysplasia
geleophysic dysplasia 2
Marfan syndrome
mitral valve prolapse
stiff skin syndrome
systemic scleroderma
Weill-Marchesani syndrome

Mouse Phenotypes
decreased body fat mass
decreased lean body mass
decreased body weight
enlarged chest
abnormal postnatal growth/weight/body size
decreased susceptibility to diet-induced obesity
increased spleen weight
Availability Mouse Genotype
Fbn1tm2Rmz/Fbn1tm2Rmz
Fbn1em1(IMPC)H/Fbn1+
Fbn1em1Chop/Fbn1+

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