SPG20 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SPG20
Gene name spastic paraplegia 20 (Troyer syndrome)
Chromosome 13
Chromosomal band q13.1
Imprinted Unknown
Genomic reference NC_000013.10
Transcript reference NM_001142294.1, NM_001142295.1, NM_001142296.1, NM_015087.4
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
Notes MSeqDR-LSDB
Date created November 12, 2013
Links to other resources
HGNC 18514
Entrez Gene 23111
PubMed articles SPG20
OMIM - Gene 607111
HGMD SPG20
GeneCards SPG20
GeneTests SPG20


Active transcripts


ID     
Chr     
Name     
NCBI ID     
NCBI Protein ID     
DescendingVariants     
00001199 13 transcript variant 4 NM_001142294.1 NP_001135766.1 0
00001200 13 transcript variant 3 NM_001142295.1 NP_001135767.1 0
00001201 13 transcript variant 2 NM_001142296.1 NP_001135768.1 0
00001202 13 transcript variant 1 NM_015087.4 NP_055902.1 0


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Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium

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