SFXN4 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SFXN4
Gene name sideroflexin 4
Chromosome 10
Chromosomal band q26.11
Imprinted Unknown
Genomic reference NC_000010.10
Transcript reference NM_213649.1, XM_005269525.1, XM_005269526.1, XM_005269527.1, XR_246070.1, XR_246071.1
Associated with diseases 615578
Citation reference(s) -
Curators (0) -
Total number of public variants reported 8
Unique public DNA variants reported 5
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
Date created November 15, 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 16088
Entrez Gene 119559
PubMed articles SFXN4
OMIM - Diseases 615578 (Combined oxidative phosphorylation deficiency 18, 615578 (3))
GeneCards SFXN4
GeneTests SFXN4

Active transcripts




NCBI ID     

NCBI Protein ID     

00002814 10 transcript variant X1 XM_005269525.1 XP_005269582.1 8
00002815 10 transcript variant X5 XR_246071.1 - 8
00002816 10 transcript variant X4 XR_246070.1 - 8
00002817 10 sideroflexin 4 NM_213649.1 NP_998814.1 8
00002818 10 transcript variant X2 XM_005269526.1 XP_005269583.1 8
00002819 10 transcript variant X3 XM_005269527.1 XP_005269584.1 8

Copyright & disclaimer
; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium