CCDC68
Coiled-coil domain-containing protein 68
Also known as: CCD68_HUMAN, SE57-1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H2F9
- Gene
- CCDC68
- Ensembl
- ENSG00000166510
- Chromosome
- 18
- Canonical length
- 335 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Cytosol
OverviewNCBI Gene
Involved in microtubule anchoring at centrosome and protein localization. Located in centriole. Part of centriolar subdistal appendage. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
335 residues, UniProt reviewed canonical sequence.
>Q9H2F9|CCDC68
1 MTTVTVTTEI PPRDKMEDNS ALYESTSAHI IEETEYVKKI RTTLQKIRTQ MFKDEIRHDS
61 TNHKLDAKHC GNLQQGSDSE MDPSCCSLDL LMKKIKGKDL QLLEMNKENE VLKIKLQASR
121 EAGAAALRNV AQRLFENYQT QSEEVRKKQE DSKQLLQVNK LEKEQKLKQH VENLNQVAEK
181 LEEKHSQITE LENLVQRMEK EKRTLLERKL SLENKLLQLK SSATYGKSCQ DLQREISILQ
241 EQISHLQFVI HSQHQNLRSV IQEMEGLKNN LKEQDKRIEN LREKVNILEA QNKELKTQVA
301 LSSETPRTKV SKAVSTSELK TEGVSPYLML IRLRKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCDC68 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)
- 0.51
- Highest tissue expression
- 31 nTPM
Expression across tissuesHPA
Tissue
- placenta: 31 nTPM
- small intestine: 23 nTPM
- duodenum: 19 nTPM
- colon: 18 nTPM
- rectum: 17 nTPM
- stomach: 14 nTPM
Single-cell type
- somatotrophs: 167 nCPM
- sertoli cells: 163 nCPM
- salivary ionocytes: 118 nCPM
- colonocytes: 116 nCPM
- enterocytes: 114 nCPM
- early spermatids: 97 nCPM
Immune cell
- non-classical monocyte: 0.2 nTPM
- basophil: 0.1 nTPM
- intermediate monocyte: 0.1 nTPM
- naive CD8 T-cell: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- hypothalamus: 7.3 nTPM
- thalamus: 6.8 nTPM
- cerebral cortex: 5 nTPM
- choroid plexus: 4.7 nTPM
- midbrain: 4.7 nTPM
- pons: 4.1 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CCDC68.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 53 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Recurrent spontaneous abortion
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)
- 1.41
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.18
- DepMap mean gene effect
- 0.14
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
InteractionsUniProt · HPA
Protein binding partners of CCDC68 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CCDC68 as an antibody target. Whether an autoantibody or antibody against CCDC68 could matter depends on whether native CCDC68 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCDC68 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 CCDC68 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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