MSeqDR-LSDB Mitochondrial Disease Locus Specific Database
SFXN4 (sideroflexin 4)
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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
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Notes
MSeqDR-LSDB
Date created
November 15, 2013
Graphical displays and utilities
Graphs
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NCBI Sequence Viewer
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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))
HGMD
SFXN4
GeneCards
SFXN4
GeneTests
SFXN4
Active transcripts
Legend
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ID
Chr
Name
NCBI ID
NCBI Protein ID
Variants
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
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