SPG21 gene homepage

General information
Gene symbol SPG21
Gene name spastic paraplegia 21 (autosomal recessive, Mast syndrome)
Chromosome 15
Chromosomal band q21-q22
Imprinted Unknown
Genomic reference NG_008992.1
Transcript reference NM_016630.3
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 56
Unique public DNA variants reported 56
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 20373
Entrez Gene 51324
PubMed articles SPG21
OMIM - Gene 608181

Active transcripts




NCBI ID     

NCBI Protein ID     

00018362 15 transcript variant 1 NM_016630.3 NP_057714.1 56