Symbol Name ID |
Atp7a
ATPase, Cu++ transporting, alpha polypeptide MGI:99400 |
Darker colors indicate more annotations |
Human Phenotypes | Gastroparesis |
Hypertonia |
Hypotonia |
EMG: neuropathic changes |
Distal muscle weakness |
Poor head control |
Distal amyotrophy |
Spinal muscular atrophy |
Disease(s) Associated with ATP7A | ||||||||
Menkes disease | ||||||||
occipital horn syndrome | ||||||||
X-linked distal spinal muscular atrophy 3 |
Mouse Phenotypes | abnormal skeletal muscle fiber morphology |
increased skeletal muscle fiber diameter |
decreased skeletal muscle mass |
calcified tendon |
muscular atrophy |
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Availability | Mouse Genotype | |||||
Atp7aMo-dp2/Atp7a+ | ||||||
Atp7atm1.2Mlke/Y | ||||||
Atp7atm1.1Mjp/Y Mnx1tm4(cre)Tmj/Mnx1+ (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 05/14/2024 MGI 6.23 |
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