Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84869
Gene name Gene Name - the full gene name approved by the HGNC.
Carbonyl reductase 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CBR4
Synonyms (NCBI Gene) Gene synonyms aliases
SDR45C1
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q32.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020570 hsa-miR-155-5p Proteomics 18668040
MIRT020570 hsa-miR-155-5p Reporter assay;Other 20584899
MIRT023498 hsa-miR-1-3p Proteomics 18668040
MIRT032121 hsa-let-7d-5p Sequencing 20371350
MIRT865736 hsa-let-7a CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003955 Function NAD(P)H dehydrogenase (quinone) activity IDA 20837989
GO:0004316 Function 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity IDA 19571038
GO:0004316 Function 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity IEA
GO:0004316 Function 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity IMP 25203508
GO:0004316 Function 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619394 25891 ENSG00000145439
Protein
UniProt ID Q8N4T8
Protein name 3-oxoacyl-[acyl-carrier-protein] reductase (EC 1.1.1.100) (3-ketoacyl-[acyl-carrier-protein] reductase beta subunit) (KAR beta subunit) (Carbonyl reductase family member 4) (CBR4) (Quinone reductase CBR4) (EC 1.6.5.10) (Short chain dehydrogenase/reductase
Protein function Component of the heterotetramer complex KAR (3-ketoacyl-[acyl carrier protein] reductase or 3-ketoacyl-[ACP] reductase) that forms part of the mitochondrial fatty acid synthase (mtFAS). Beta-subunit of the KAR heterotetramer complex, responsible
PDB 4CQL , 4CQM
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13561 adh_short_C2 8 234 Domain
Tissue specificity TISSUE SPECIFICITY: Detected in liver and kidney (at protein level) (PubMed:19000905). Displays the highest expression in neuronal and muscle tissues (PubMed:25203508). {ECO:0000269|PubMed:19000905, ECO:0000303|PubMed:25203508}.
Sequence
Sequence length 237
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Fatty acid biosynthesis
Metabolic pathways
Fatty acid metabolism
  Fatty acyl-CoA biosynthesis
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Cerebral amyloid angiopathy Cerebral amyloid angiopathy N/A N/A GWAS
Glioblastoma Glioblastoma N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS