Seroatlas · Human Serome Atlas

CIMIP2C

Ciliary microtubule inner protein 2C

Also known as: C2orf70, CMI2C_HUMAN, FAM166C, LOC339778

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

Protein identityUniProt · HPA

UniProt accession
A6NJV1
Gene
CIMIP2C
Ensembl
ENSG00000173557
Chromosome
2
Canonical length
201 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nuclear membrane,Vesicles

OverviewNCBI Gene

Predicted to be involved in flagellated sperm motility. Located in axonemal microtubule. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

201 residues, UniProt reviewed canonical sequence.

>A6NJV1|CIMIP2C
     1  MASRSAGTLL TEFNAAYVPP GLMPGYQGHV PTVAFSFGAP YGTTTLKYFQ DHRNRAMEKS
    61  HTPFSQGGHF PTIFSTNPNL LLMERASTRD RWLHKPSYTR FNLDSHRSTE LTNFYQMVQQ
   121  HRKYYQDKTG TVPRVPYFAM PVREPERYPL PTVLPPLCPK KKWHLLRLAP ENLKTYQTFP
   181  SGKRVSPQER KKRDCYFEFR A

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CIMIP2C 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)
0.52
Highest tissue expression
25 nTPM

Expression across tissuesHPA

Tissue

  • testis: 25 nTPM
  • choroid plexus: 8.2 nTPM
  • fallopian tube: 7.1 nTPM
  • stomach: 4.5 nTPM
  • hypothalamus: 2.4 nTPM
  • salivary gland: 1.8 nTPM

Single-cell type

  • late spermatids: 611 nCPM
  • early spermatids: 156 nCPM
  • late primary spermatocytes: 104 nCPM
  • fallopian tube ciliated cells: 45 nCPM
  • epididymal efferent duct ciliated cells: 38 nCPM
  • respiratory ciliated cells: 29 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: 8.4 nTPM
  • hypothalamus: 5.9 nTPM
  • medulla oblongata: 4.1 nTPM
  • midbrain: 4.1 nTPM
  • spinal cord: 2.8 nTPM
  • pons: 1.6 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)
1.58
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 5% 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

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CIMIP2C as an antibody target. Whether an autoantibody or antibody against CIMIP2C could matter depends on whether native CIMIP2C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CIMIP2C 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 CIMIP2C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CIMIP2C. 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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