GENOTYPE
pc21Tg
- ID
- ZDB-GENO-150224-1
- Name
- pc21Tg
- Previous Name
- Background
- Unspecified
- Affected Genomic Region
- Current Source
- No data available
Notes
Genotype Composition
| Genomic Feature | Construct | Lab of Origin | Zygosity | Parental Zygosity |
|---|---|---|---|---|
| pc21Tg | Tg(actc1b:LIFEACT-EGFP) | Peter Currie Lab | unknown | Unknown |
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Fish utilizing pc21Tg
- Sztal, T.E., McKaige, E.A., Williams, C., Oorschot, V., Ramm, G., Bryson-Richardson, R.J. (2018) Testing of therapies in a novel nebulin nemaline myopathy model demonstrate a lack of efficacy. Acta neuropathologica communications. 6:40
- Berger, J., Berger, S., Li, M., Currie, P.D. (2017) Myo18b is essential for sarcomere assembly in fast skeletal muscle. Human molecular genetics. 26(6):1146-1156
- Mukherjee, K., Ishii, K., Pillalamarri, V., Kammin, T., Atkin, J.F., Hickey, S.E., Xi, Q.J., Gusella, J.F., Talkowski, M.E., Morton, C.C., Maas, R.L., Liao, E.C. (2016) Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis. Human molecular genetics. 25(7):1255-70
- Berger, J., Tarakci, H., Berger, S., Li, M., Hall, T.E., Arner, A., Currie, P.D. (2014) Loss of tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy. Disease models & mechanisms. 7(12):1407-15
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