Symbol Name ID |
Mef2c
myocyte enhancer factor 2C MGI:99458 |
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 |
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Availability | Mouse Genotype | |||||||||||||||||||
Mef2ctm1Eno/Mef2c+ | ||||||||||||||||||||
Tg(Col2a1-Mef2c/VP16)1Eno/0 | ||||||||||||||||||||
Mef2ctm1Eno/Mef2ctm1Jjs H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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Mef2ctm1Eno/Mef2ctm2Eno Twist2tm1(cre)Dor/Twist2+ (conditional) |
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Mef2ctm1Eno/Mef2ctm2Eno Tg(Col2a1-cre)1Bhr/0 (conditional) |
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 |
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