Seroatlas · Human Serome Atlas

CIMIP6

Ciliary microtubule inner protein 6

Also known as: C2orf73, CMIP6_HUMAN, FLJ40298

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

Protein identityUniProt · HPA

UniProt accession
Q8N5S3
Gene
CIMIP6
Ensembl
ENSG00000177994
Chromosome
2
Canonical length
287 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nucleoplasm,Plasma membrane,Cytosol

OverviewNCBI Gene

Predicted to be located in cilium. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

287 residues, UniProt reviewed canonical sequence.

>Q8N5S3|CIMIP6
     1  MEEKEDKHQQ HKIEDAAITY VSENEEIKHE EKPGKSIHHS KSHVGRGRIY YAKFINTNAR
    61  TYNEPFPYID PKKGPEIQGD WWSHGKALEP VFLPPYDSKS TQRSDFQKPS CPLVLPVKHS
   121  KMQKPSCGIV PLASPGTSAE LQNNFIEYIS FIHQYDARKT PNEPLQGKRH GAFVQREIKP
   181  GSRPTVPKGA EVLLNTPGSR SSEQSKKTEK GNSAESRMIS PGLCQQNSQE LLEPKTHLSE
   241  TDVRQAAKAC PSTPESREKT SGATQTTVGD ALFTRHKPLN PPIKKSE

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CIMIP6 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)
0.66
Highest tissue expression
46 nTPM

Expression across tissuesHPA

Tissue

  • testis: 46 nTPM
  • fallopian tube: 7.1 nTPM
  • choroid plexus: 3.7 nTPM
  • basal ganglia: 1.4 nTPM
  • hypothalamus: 1.4 nTPM
  • amygdala: 1.2 nTPM

Single-cell type

  • early spermatids: 1,279 nCPM
  • late spermatids: 738 nCPM
  • late primary spermatocytes: 534 nCPM
  • ependymal cells: 198 nCPM
  • respiratory ciliated cells: 165 nCPM
  • choroid plexus epithelial cells: 164 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • choroid plexus: 12 nTPM
  • medulla oblongata: 7 nTPM
  • midbrain: 6.2 nTPM
  • spinal cord: 5.5 nTPM
  • white matter: 3.5 nTPM
  • pons: 3.4 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)
1.62
gnomAD pLI
0
DepMap mean gene effect
0.02
DepMap dependency class
none

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

Cellular components

Protein domainsUniProt · Pfam · InterPro

  • Ciliary microtubule inner protein 6
  • Ciliary microtubule inner protein 6

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CIMIP6 as an antibody target. Whether an autoantibody or antibody against CIMIP6 could matter depends on whether native CIMIP6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CIMIP6 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 CIMIP6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CIMIP6. 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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