Seroatlas · Human Serome Atlas

ALKBH7

Alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial

Also known as: ALKB7_HUMAN, MGC10974, SPATA11

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q9BT30
Gene
ALKBH7
Ensembl
ENSG00000125652
Chromosome
19
Canonical length
221 aa
Protein class
Predicted intracellular proteins
Subcellular location
Mitochondria

OverviewNCBI Gene

Predicted to enable dioxygenase activity and metal ion binding activity. Involved in DNA damage response and regulation of mitochondrial membrane permeability involved in programmed necrotic cell death. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

221 residues, UniProt reviewed canonical sequence.

>Q9BT30|ALKBH7
     1  MAGTGLLALR TLPGPSWVRG SGPSVLSRLQ DAAVVRPGFL STAEEETLSR ELEPELRRRR
    61  YEYDHWDAAI HGFRETEKSR WSEASRAILQ RVQAAAFGPG QTLLSSVHVL DLEARGYIKP
   121  HVDSIKFCGA TIAGLSLLSP SVMRLVHTQE PGEWLELLLE PGSLYILRGS ARYDFSHEIL
   181  RDEESFFGER RIPRGRRISV ICRSLPEGMG PGESGQPPPA C

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against ALKBH7 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)
0.29
Highest tissue expression
518 nTPM

Expression across tissuesHPA

Tissue

  • testis: 518 nTPM
  • liver: 163 nTPM
  • heart muscle: 159 nTPM
  • skeletal muscle: 145 nTPM
  • pancreas: 112 nTPM
  • kidney: 94 nTPM

Single-cell type

  • late spermatids: 13,357 nCPM
  • late primary spermatocytes: 3,371 nCPM
  • early spermatids: 2,932 nCPM
  • enterocytes: 770 nCPM
  • colonocytes: 545 nCPM
  • esophageal apical cells: 484 nCPM

Immune cell

  • plasmacytoid DC: 144 nTPM
  • naive CD4 T-cell: 138 nTPM
  • myeloid DC: 128 nTPM
  • memory B-cell: 114 nTPM
  • naive CD8 T-cell: 112 nTPM
  • classical monocyte: 107 nTPM

Brain region

  • choroid plexus: 78 nTPM
  • white matter: 74 nTPM
  • cerebellum: 70 nTPM
  • spinal cord: 66 nTPM
  • medulla oblongata: 66 nTPM
  • thalamus: 62 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)
1.63
gnomAD pLI
0
gnomAD missense Z
0.13
DepMap mean gene effect
-0.08
DepMap dependency class
selective

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

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads ALKBH7 as an antibody target. Whether an autoantibody or antibody against ALKBH7 could matter depends on whether native ALKBH7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

ALKBH7 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 ALKBH7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/ALKBH7. 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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