Seroatlas · Human Serome Atlas

HOATZ

Cilia- and flagella-associated protein HOATZ

Also known as: C11orf88, FLJ46266, HOATZ_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q6PI97
Gene
HOATZ
Ensembl
ENSG00000183644
Chromosome
11
Canonical length
169 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

Predicted to be involved in axoneme assembly; flagellated sperm motility; and spermatogenesis. Predicted to be located in cilium and cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

169 residues, UniProt reviewed canonical sequence.

>Q6PI97|HOATZ
     1  METGPSEEPS GRKESQEMCP PGLLVFAGSS EQDANLAKQF WISASMYPPS ESQLVLRRDS
    61  SQRLPVARPR RSRGSENSHS SQSFHLASNK NRDIFAEALK IQESEEKVKY LQKAKTREEI
   121  LQLLRKQREE RISKELISLP YKPKAKEHKA KKVVSESDKE DQEEVKTLD

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against HOATZ 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)
0.61
Highest tissue expression
159 nTPM

Expression across tissuesHPA

Tissue

  • choroid plexus: 159 nTPM
  • fallopian tube: 81 nTPM
  • testis: 27 nTPM
  • hypothalamus: 13 nTPM
  • hippocampal formation: 13 nTPM
  • basal ganglia: 12 nTPM

Single-cell type

  • fallopian tube ciliated cells: 1,080 nCPM
  • respiratory ciliated cells: 1,028 nCPM
  • endometrial ciliated cells: 870 nCPM
  • epididymal efferent duct ciliated cells: 432 nCPM
  • late primary spermatocytes: 311 nCPM
  • ependymal cells: 179 nCPM

Immune cell

  • neutrophil: 0.4 nTPM
  • basophil: 0.3 nTPM
  • eosinophil: 0.2 nTPM
  • memory B-cell: 0.1 nTPM
  • naive B-cell: 0.1 nTPM
  • naive CD8 T-cell: 0.1 nTPM

Brain region

  • choroid plexus: 68 nTPM
  • midbrain: 26 nTPM
  • medulla oblongata: 23 nTPM
  • spinal cord: 15 nTPM
  • white matter: 13 nTPM
  • pons: 8.5 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)
1.16
gnomAD pLI
0
DepMap mean gene effect
-0.06
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Cellular components

Protein domainsUniProt · Pfam · InterPro

  • Cilia- and flagella-associated protein HOATZ-like
  • Cilia- and flagella-associated protein HOATZ-like

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

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

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

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