Seroatlas · Human Serome Atlas

CCDC71

Coiled-coil domain-containing protein 71

Also known as: CCD71_HUMAN, FLJ12800

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

Protein identityUniProt · HPA

UniProt accession
Q8IV32
Gene
CCDC71
Ensembl
ENSG00000177352
Chromosome
3
Canonical length
467 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nuclear membrane

OverviewNCBI Gene

No narrative summary is available for CCDC71 in this catalog release; identity and structured annotations are shown without generated factual claims.

Canonical amino-acid sequenceUniProt

467 residues, UniProt reviewed canonical sequence.

>Q8IV32|CCDC71
     1  MSVVVQHVEE KAVHSWSRIS TAGKKALEEA LLVFNPMSQD LSATEAQLVA FLQGLRDDGF
    61  QPTILRSGDV YGYSSCTANP PSQTKLQARA PNPTATSPPA SAPRTAMRLP AGRATLLPMP
   121  LSGRLAKAST PALAKHATTN LLLSSLKQSS ASHARGAAVG FPTHLYPGVY PAMRLSVVLE
   181  ALVPLKTPMP CLGAKHKAQS LQLSLADSPL KLRKSSGKGP GNPRPKAPRK TTSKGPKCLT
   241  RKGPGAGPRR GSGHQSKTNR ATGSPSVRRM KGGSALGTKT AQAKVARTLA KAARAQAKVA
   301  RTQAKAAKAR AKAKAAQVKA KAKAKAAQVK AKAKVMAAWA KAKAKAKAVR AKAKVARTQP
   361  RGRGRPKGSA KARTTRKGQK NRPETVGQKR KRAEEAKDLP PKKRTRLGPR SPKAWLGPGT
   421  AKLLKFRAIK VDRRSSDDEV RQRAQRILRV NLSPVIRLQP LLPYSAV

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CCDC71 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
Unknown
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.64
Highest tissue expression
19 nTPM

Expression across tissuesHPA

Tissue

  • ovary: 19 nTPM
  • fallopian tube: 15 nTPM
  • thyroid gland: 15 nTPM
  • adrenal gland: 15 nTPM
  • endometrium: 14 nTPM
  • skeletal muscle: 14 nTPM

Single-cell type

  • epididymal principal cells: 33 nCPM
  • decidual stromal cells: 29 nCPM
  • migrating cytotrophoblasts: 27 nCPM
  • cytotrophoblasts: 26 nCPM
  • syncytiotrophoblasts: 26 nCPM
  • hofbauer cells: 25 nCPM

Immune cell

  • NK-cell: 4.8 nTPM
  • intermediate monocyte: 1.7 nTPM
  • MAIT T-cell: 1.4 nTPM
  • naive B-cell: 1.3 nTPM
  • non-classical monocyte: 1.3 nTPM
  • memory CD8 T-cell: 1.2 nTPM

Brain region

  • hypothalamus: 12 nTPM
  • midbrain: 11 nTPM
  • medulla oblongata: 11 nTPM
  • spinal cord: 11 nTPM
  • basal ganglia: 11 nTPM
  • cerebellum: 11 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)
0.76
gnomAD pLI
0.03
gnomAD missense Z
-0.36
DepMap mean gene effect
-0.13
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).

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CCDC71 as an antibody target. Whether an autoantibody or antibody against CCDC71 could matter depends on whether native CCDC71 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CCDC71 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 CCDC71 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CCDC71. 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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