Tissue expression
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Protein structure

DDHD1

DDHD domain containing 1
KIAA1705, PA-PLA1, SPG28 
This gene is a member of the intracellular phospholipase A1 gene family. The protein encoded by this gene preferentially hydrolyzes phosphatidic acid. It is a cytosolic protein with some mitochondrial localization, and is thought to be involved in the regulation of mitochondrial dynamics. Overexpression of this gene causes fragmentation of the tubular structures in mitochondria, while depletion of the gene results in mitochondrial tubule elongation. Deletion of this gene in male mice caused fertility defects, resulting from disruption in the organization of the mitochondria during spermiogenesis. In humans, mutations in this gene have been associated with hereditary spastic paraplegia (HSP), also known as Strumpell-Lorrain disease, or, familial spastic paraparesis (FSP). This inherited disorder is characterized by progressive weakness and spasticity of the legs. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]
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48 antibodies from 9 providers.

Antibody properties

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AntibodyRefsTypeWBELICCIPIHCFC
Atlas Antibodies
1 antibody
Invitrogen Antibodies
3 antibodies
Biorbyt
12 antibodies
antibodies-online
5 antibodies
Novus Biologicals
3 antibodies
Bethyl Laboratories
1 antibody
Abnova Corporation
5 antibodies
Creative Diagnostics
4 antibodies