Gene Gene information from NCBI Gene database.
Entrez ID 56901
Gene name Cytochrome c oxidase hypoxia associated subunit FA4L2
Gene symbol COXFA4L2
Synonyms (NCBI Gene)
MISTRHNDUFA4L2NUOMS
Chromosome 12
Chromosome location 12q13.3
miRNA miRNA information provided by mirtarbase database.
45
miRTarBase ID miRNA Experiments Reference
MIRT017521 hsa-miR-335-5p Microarray 18185580
MIRT1178777 hsa-miR-1285 CLIP-seq
MIRT1178778 hsa-miR-1291 CLIP-seq
MIRT1178779 hsa-miR-1321 CLIP-seq
MIRT1178780 hsa-miR-2053 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005739 Component Mitochondrion HTP 34800366
GO:0045277 Component Respiratory chain complex IV IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NRX3
Protein name NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 4-like 2 (NADH-ubiquinone oxidoreductase MLRQ subunit homolog) (NUOMS)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06522 B12D 16 84 NADH-ubiquinone reductase complex 1 MLRQ subunit Family
Sequence
Sequence length 87
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Oxidative phosphorylation
Metabolic pathways
Thermogenesis
Retrograde endocannabinoid signaling
Non-alcoholic fatty liver disease
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy