AKR7A3
Aldo-keto reductase family 7 member A3
Also known as: ARK73_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95154
- Gene
- AKR7A3
- Ensembl
- ENSG00000162482
- Chromosome
- 1
- Canonical length
- 331 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Aldo-keto reductases, such as AKR7A3, are involved in the detoxification of aldehydes and ketones.[supplied by OMIM, Apr 2004]
Canonical amino-acid sequenceUniProt
331 residues, UniProt reviewed canonical sequence.
>O95154|AKR7A3
1 MSRQLSRARP ATVLGAMEMG RRMDAPTSAA VTRAFLERGH TEIDTAFVYS EGQSETILGG
61 LGLRLGGSDC RVKIDTKAIP LFGNSLKPDS LRFQLETSLK RLQCPRVDLF YLHMPDHSTP
121 VEETLRACHQ LHQEGKFVEL GLSNYAAWEV AEICTLCKSN GWILPTVYQG MYNAITRQVE
181 TELFPCLRHF GLRFYAFNPL AGGLLTGKYK YEDKNGKQPV GRFFGNTWAE MYRNRYWKEH
241 HFEGIALVEK ALQAAYGASA PSMTSATLRW MYHHSQLQGA HGDAVILGMS SLEQLEQNLA
301 AAEEGPLEPA VVDAFNQAWH LVTHECPNYF RLocalizationUniProt · AlphaFold · HPA
Whether an antibody against AKR7A3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.23
- Highest tissue expression
- 400 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 400 nTPM
- stomach: 306 nTPM
- duodenum: 234 nTPM
- liver: 218 nTPM
- small intestine: 136 nTPM
- kidney: 86 nTPM
Single-cell type
- parietal cells: 1,425 nCPM
- enterocytes: 955 nCPM
- gastric chief cells: 262 nCPM
- enteric transient amplifying cells: 182 nCPM
- pancreatic acinar cells: 150 nCPM
- colonocytes: 134 nCPM
Immune cell
- plasmacytoid DC: 0.3 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- choroid plexus: 35 nTPM
- hippocampal formation: 6.8 nTPM
- thalamus: 6.2 nTPM
- midbrain: 6 nTPM
- cerebellum: 5.7 nTPM
- medulla oblongata: 5.6 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.93
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.17
- DepMap mean gene effect
- -0.21
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- alcohol dehydrogenase (NADP+) activity
- electron transfer activity
- identical protein binding
- NADP+ binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of AKR7A3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads AKR7A3 as an antibody target. Whether an autoantibody or antibody against AKR7A3 could matter depends on whether native AKR7A3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
AKR7A3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label AKR7A3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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