Spg21 - SPG21 abhydrolase domain containing, maspardin Gene

Rattus norvegicus

Gene ID: 300791 | Gene type: protein coding

About Spg21

Summary

Predicted to enable CD4 receptor binding activity. Predicted to be located in intracellular membrane-bounded organelle. Predicted to be active in cytosol and trans-Golgi network transport vesicle. Human ortholog(s) of this gene implicated in Mast syndrome and hereditary spastic paraplegia. Orthologous to human SPG21 (SPG21 abhydrolase domain containing, maspardin). [provided by Alliance of Genome Resources, Apr 2022]

Spg21 Products(3)

mRNA	Protein	Name
NM_001006987.2	NP_001006988.1	maspardin isoform 3
NM_001413543.1	NP_001400472.1	maspardin isoform 1
NM_001413544.1	NP_001400473.1	maspardin isoform 2

Protein Preferred Names

Protein Names

maspardin

SPG21, maspardin	acid cluster protein 33
spastic paraplegia 21 autosomal recessive Mast syndrome protein homolog	spastic paraplegia 21 homolog
spastic paraplegia 21 homolog-like

Related Agents

Pre-clinical Phase

Bioactive Molecules (3)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13662	SPG21 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown
HY-RS20496	Spg21 Mouse Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown
HY-RS27004	Spg21 Rat Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Spg21	NCBI	NCBI:51324
Mus musculus	Spg21	NCBI	NCBI:27965

Name
Email *

	Sorry, but the email address you supplied was invalid.