Seroatlas · Human Serome Atlas

AKR7L

Aflatoxin B1 aldehyde reductase member 4

Also known as: ARK74_HUMAN

Cross-references: UniProt · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q8NHP1
Gene
AKR7L
Canonical length
331 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

No narrative summary is available for AKR7L in this catalog release; identity and structured annotations are shown without generated factual claims.

Canonical amino-acid sequenceUniProt

331 residues, UniProt reviewed canonical sequence.

>Q8NHP1|AKR7L
     1  MSRQLSRARP ATVLGAMEMG RRMDAPTSAA VTRAFLERGH TEIDTAFLYS DGQSETILGG
    61  LGLRMGSSDC RVKIATKANP WIGNSLKPDS VRSQLETSLK RLQCPRVDLF YLHAPDHSAP
   121  VEETLRACHQ LHQEGKFVEL GLSNYAAWEV AEICTLCKSN GWILPTVYQG MYSATTRQVE
   181  TELFPCLRHF GLRFYAYNPL AGGLLTGKYK YEDKDGKQPV GRFFGTQWAE IYRNHFWKEH
   241  HFEGIALVEK ALQAAYGASA PSMTSAALRW MYHHSQLQGA HGDAVILGMS SLEQLEQNLA
   301  AAEEGPLEPA VVDAFNQAWH LFAHECPNYF I

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against AKR7L 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
58 nTPM

Expression across tissuesHPA

Tissue

  • duodenum: 58 nTPM
  • small intestine: 45 nTPM
  • liver: 35 nTPM
  • stomach: 24 nTPM
  • kidney: 7.6 nTPM
  • colon: 4.9 nTPM

Single-cell type

  • enterocytes: 60 nCPM
  • foveolar cells: 19 nCPM
  • hepatocytes: 17 nCPM
  • mucous neck cells: 14 nCPM
  • enteric transient amplifying cells: 7.8 nCPM
  • pancreatic acinar cells: 7.8 nCPM

Immune cell

  • basophil: 0.3 nTPM
  • neutrophil: 0.3 nTPM
  • classical monocyte: 0.2 nTPM
  • myeloid DC: 0.2 nTPM
  • plasmacytoid DC: 0.2 nTPM
  • T-reg: 0.2 nTPM

Brain region

  • choroid plexus: 10 nTPM
  • cerebellum: 9.8 nTPM
  • cerebral cortex: 7 nTPM
  • hippocampal formation: 6.9 nTPM
  • amygdala: 6.5 nTPM
  • basal ganglia: 6.4 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)
1.59
gnomAD pLI
0
gnomAD missense Z
0.26

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads AKR7L as an antibody target. Whether an autoantibody or antibody against AKR7L could matter depends on whether native AKR7L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

AKR7L 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 AKR7L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/AKR7L. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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