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Gene: FMC1-LUC7L2 (FMC1-LUC7L2 readthrough) Homo sapiens
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Symbol: FMC1-LUC7L2
Name: FMC1-LUC7L2 readthrough
Description: Predicted to have mRNA binding activity. Involved in mitochondrial proton-transporting ATP synthase complex assembly. Localizes to the mitochondrion.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: ATP synthase assembly factor FMC1, mitochondrial; C7orf55; C7orf55-LUC7L2; C7orf55-LUC7L2 readthrough; FMC1; Formation of mitochondrial complex V assembly factor 1 homolog
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387139,341,132 - 139,423,457 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377139,025,878 - 139,108,203 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map7q34NCBI
HuRef7133,335,761 - 133,418,085 (+)NCBIHuRef
CHM1_17138,959,615 - 139,041,959 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FMC1-LUC7L2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 7255398
Created: 2013-08-20
Species: Homo sapiens
Last Modified: 2019-11-26
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.