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Symbol
Name
ID
Fbn2
fibrillin 2
MGI:95490
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Arthrogryposis multiplex congenita
Congenital finger flexion contractures
Distal arthrogryposis
Arthrogryposis-like hand anomaly
Camptodactyly
Camptodactyly of finger
Camptodactyly of 2nd-5th fingers
Camptodactyly of toe
Flexion contracture of finger
Flexion contracture of toe
Joint contractures involving the joints of the feet
Contractures involving the joints of the feet
Plantar flexion contractures
Hamstring contractures
Hip contracture
Knee flexion contracture
Elbow flexion contracture
Joint contracture of the hand
Shoulder flexion contracture
Wrist flexion contracture
Restricted neck movement due to contractures
Torticollis
Calf muscle hypoplasia
Decreased muscle mass
Firm muscles
Muscle weakness
Disease(s) Associated with FBN2
distal arthrogryposis

Mouse Phenotypes
decreased skeletal muscle fiber diameter
centrally nucleated skeletal muscle fibers
increased skeletal muscle mass
abnormal muscle electrophysiology
muscle weakness
Availability Mouse Genotype
Fbn2fp/Fbn2fp
Fbn2mz/Fbn2mz
Fbn2fp/Fbn2mz

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
08/13/2019
MGI 6.14
The Jackson Laboratory