ATP5G1 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB

General information
Gene symbol	ATP5G1
Gene name	ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9)
Chromosome	17
Chromosomal band	q21.32
Imprinted	Unknown
Genomic reference	NC_000017.10
Transcript reference	NM_001002027.1, NM_005175.2
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	841
Entrez Gene	516
PubMed articles	ATP5G1
OMIM - Gene	603192
HGMD	ATP5G1
GeneCards	ATP5G1
GeneTests	ATP5G1

Active transcripts

Legend

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ID	Chr	Name	NCBI ID	NCBI Protein ID	Variants
00000494	17	transcript variant 1	NM_005175.2	NP_005166.1	0
00000495	17	transcript variant 2	NM_001002027.1	NP_001002027.1	0

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; NuclearMitome http://www.transgenomic.com ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium

MSeqDR-LSDB Mitochondrial Disease Locus Specific Database

ATP5G1 (ATP synthase, H+ transporting, mitochondria...)

ATP5G1 gene homepage

Active transcripts

Legend