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Symbol
Name
ID
Fermt2
fermitin family member 2
MGI:2385001
Phenotype annotations related to skeleton
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations

Mouse Phenotypes
skeleton phenotype
increased chondrocyte apoptosis
decreased chondrocyte proliferation
absent neurocranium
brachyphalangia
short humerus
short radius
short ulna
decreased femur compact bone thickness
short femur
short tibia
abnormal skeleton morphology
small clavicle
clavicle hypoplasia
abnormal long bone epiphyseal plate morphology
abnormal long bone epiphyseal plate proliferative zone
abnormal long bone hypertrophic chondrocyte zone
disorganized long bone epiphyseal plate
decreased length of long bones
abnormal scapula morphology
short scapula
abnormal sternum morphology
sternebra fusion
short sternum
wide sternum
small thoracic cage
kyphosis
vertebral compression
small vertebrae
decreased bone mineral density
decreased trabecular bone volume
abnormal chondrocyte morphology
decreased chondrocyte number
chondrodystrophy
delayed endochondral bone ossification
abnormal intramembranous bone ossification
Availability Mouse Genotype
Fermt2tm1.1Gxo/Fermt2tm1.1Gxo
Tg(Prrx1-cre)1Cjt/0  (conditional)
Fermt2tm1.1Gxo/Fermt2tm1.1Gxo
Tg(Col2a1-cre)1Bhr/0  (conditional)
*

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
04/30/2024
MGI 6.23
The Jackson Laboratory