Symbol Name ID |
Myh8
myosin, heavy polypeptide 8, skeletal muscle, perinatal MGI:1339712 |
Darker colors indicate more annotations |
Human Phenotypes | Micrognathia |
Mandibular prognathia |
Trismus |
Microcephaly |
Mild microcephaly |
Macrocephaly |
Symphalangism affecting the phalanges of the hand |
Hammertoe |
Cutaneous syndactyly of toes |
Metatarsus adductus |
Foot joint contracture |
Hip dislocation |
Joint contracture of the hand |
Arthrogryposis multiplex congenita |
Distal arthrogryposis |
Limitation of joint mobility |
Disease(s) Associated with MYH8 | ||||||||||||||||
distal arthrogryposis type 7 |
Mouse Phenotypes | abnormal sternum morphology |
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Availability | Mouse Genotype | |
Myh8em1(IMPC)Tcp/Myh8+ |
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 09/03/2024 MGI 6.24 |
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