Symbol Name ID |
Neb
nebulin MGI:97292 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased fetal movement |
Feeding difficulties |
Disease(s) Associated with NEB | ||
arthrogryposis multiplex congenita-6 | ||
nemaline myopathy 2 |
Mouse Phenotypes | abnormal suckling behavior |
decreased grip strength |
abnormal gait |
decreased locomotor activity |
impaired exercise endurance |
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Availability | Mouse Genotype | |||||
Nebtm1(cre)Chen/Nebtm1(cre)Chen | ||||||
Nebtm1Slbt/Nebtm1Slbt | ||||||
Nebm1Anu/Nebm2Anu | ||||||
Nebtm2Hgra/Nebtm2Hgra Tg(Ckmm-cre)5Khn/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 04/30/2024 MGI 6.23 |
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