Morpholino
MO1-slc25a46
- ID
- ZDB-MRPHLNO-151102-1
- Name
- MO1-slc25a46
- Previous Names
- None
- Target
- Sequence
-
5' - CAGTGTCTTATTCTGCATACCTGAC - 3'
- Disclaimer
- Although ZFIN verifies reagent sequence data, we recommend that you conduct independent sequence analysis before ordering any reagent.
- Note
-
Splice-blocking MO.
- Genome Resources
- None
Target Location
Genomic Features
No data available
Expression
Gene expression in Wild Types + MO1-slc25a46
No data available
Phenotype
Phenotype resulting from MO1-slc25a46
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Phenotype of all Fish created by or utilizing MO1-slc25a46
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Citations
- Wan, J., Steffen, J., Yourshaw, M., Mamsa, H., Andersen, E., Rudnik-Schöneborn, S., Pope, K., Howell, K.B., McLean, C.A., Kornberg, A.J., Joseph, J., Lockhart, P.J., Zerres, K., Ryan, M.M., Nelson, S.F., Koehler, C.M., Jen, J.C. (2016) Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia. Brain : a journal of neurology. 139(11):2877-2890
- Abrams, A.J., Hufnagel, R.B., Rebelo, A., Zanna, C., Patel, N., Gonzalez, M.A., Campeanu, I.J., Griffin, L.B., Groenewald, S., Strickland, A.V., Tao, F., Speziani, F., Abreu, L., Schüle, R., Caporali, L., La Morgia, C., Maresca, A., Liguori, R., Lodi, R., Ahmed, Z.M., Sund, K.L., Wang, X., Krueger, L.A., Peng, Y., Prada, C.E., Prows, C.A., Schorry, E.K., Antonellis, A., Zimmerman, H.H., Abdul-Rahman, O.A., Yang, Y., Downes, S.M., Prince, J., Fontanesi, F., Barrientos, A., Németh, A.H., Carelli, V., Huang, T., Zuchner, S., Dallman, J.E. (2015) Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature Genetics. 47(8):926-32
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