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Symbol
Name
ID
Mef2c
myocyte enhancer factor 2C
MGI:99458
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Clinodactyly of the 5th finger
2-3 toe syndactyly
Disease(s) Associated with MEF2C
neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language

Mouse Phenotypes
Meckel's cartilage hypoplasia
abnormal neurocranium morphology
temporal bone hypoplasia
zygomatic arch hypoplasia
abnormal mandibular angle morphology
mandibular condyloid process hypoplasia
mandibular coronoid process hypoplasia
mandible hypoplasia
short mandible
short fibula
short tibia
decreased length of long bones
failure of sternum ossification
abnormal trabecular bone morphology
abnormal epiphyseal plate morphology
abnormal endochondral bone ossification
failure of endochondral bone ossification
premature endochondral bone ossification
delayed bone ossification
Availability Mouse Genotype
Mef2ctm1Eno/Mef2c+
Tg(Col2a1-Mef2c/VP16)1Eno/0
Mef2ctm1Eno/Mef2ctm1Jjs
H2az2Tg(Wnt1-cre)11Rth/H2az2+  (conditional)
Mef2ctm1Eno/Mef2ctm2Eno
Twist2tm1(cre)Dor/Twist2+  (conditional)
Mef2ctm1Eno/Mef2ctm2Eno
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
04/16/2024
MGI 6.23
The Jackson Laboratory