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General Information
ZFIN ID: ZDB-FIG-121003-1
Zivony-Elboum et al., 2012 - A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis. Journal of Medical Genetics   49(7):462-472 Full text @ J. Med. Genet.
Knockdown Reagent:
Observed In:
Stage: Day 4

Fig. 4 ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions.

Gene Expression DetailsNo data available
Antibody Labeling Details No data available
Phenotype Details
Fish Conditions Stage Phenotype
AB/TL + MO2-vps37a standard conditions Day 4 whole organism decreased mobility, abnormal
Day 4 whole organism morphology, normal
Full text @ J. Med. Genet.