CCDC34
Coiled-coil domain-containing protein 34
Also known as: CCD34_HUMAN, L15, NY-REN-41, RAMA3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96HJ3
- Gene
- CCDC34
- Ensembl
- ENSG00000109881
- Chromosome
- 11
- Canonical length
- 373 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nuclear membrane,Nucleoli fibrillar center,Calyx,Connecting piece,Mid piece,Principal piece,End piece
OverviewNCBI Gene
Involved in spermatogenesis. Located in sperm midpiece. Implicated in spermatogenic failure 76. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
373 residues, UniProt reviewed canonical sequence.
>Q96HJ3|CCDC34
1 MWAAGRWGPT FPSSYAGFSA DCRPRSRPSS DSCSVPMTGA RGQGLEVVRS PSPPLPLSCS
61 NSTRSLLSPL GHQSFQFDED DGDGEDEEDV DDEEDVDEDA HDSEAKVASL RGMELQGCAS
121 TQVESENNQE EQKQVRLPES RLTPWEVWFI GKEKEERDRL QLKALEELNQ QLEKRKEMEE
181 REKRKIIAEE KHKEWVQKKN EQKRKEREQK INKEMEEKAA KELEKEYLQE KAKEKYQEWL
241 KKKNAEECER KKKEKEKEKQ QQAEIQEKKE IAEKKFQEWL ENAKHKPRPA AKSYGYANGK
301 LTGFYSGNSY PEPAFYNPIP WKPIHMPPPK EAKDLSGRKS KRPVISQPHK SSSLVIHKAR
361 SNLCLGTLCR IQRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCDC34 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)
- 0.62
- Highest tissue expression
- 48 nTPM
Expression across tissuesHPA
Tissue
- testis: 48 nTPM
- choroid plexus: 21 nTPM
- basal ganglia: 15 nTPM
- thymus: 15 nTPM
- cerebral cortex: 14 nTPM
- bone marrow: 13 nTPM
Single-cell type
- late primary spermatocytes: 607 nCPM
- early spermatids: 324 nCPM
- differentiating spermatogonia: 272 nCPM
- early primary spermatocytes: 212 nCPM
- epididymal efferent duct ciliated cells: 169 nCPM
- undifferentiated spermatogonia: 156 nCPM
Immune cell
- T-reg: 6.7 nTPM
- naive CD4 T-cell: 4.5 nTPM
- memory CD8 T-cell: 4.2 nTPM
- naive B-cell: 4 nTPM
- memory CD4 T-cell: 3.9 nTPM
- NK-cell: 3.8 nTPM
Brain region
- choroid plexus: 12 nTPM
- cerebral cortex: 11 nTPM
- amygdala: 9.9 nTPM
- hippocampal formation: 9.5 nTPM
- hypothalamus: 9.5 nTPM
- basal ganglia: 9.4 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CCDC34.
Disease | AllUniProt
Conditions CCDC34 is implicated in, by any mechanism.
- Spermatogenic failure 76 (SPGF76) MIM:620084
Disease | GeneticClinVar
3 pathogenic / likely-pathogenic of 52 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Spermatogenic failure 76
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)
- 1.02
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.26
- 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
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Coiled-coil domain-containing protein 34/181
- Coiled-coil domain-containing protein 34
- Coiled-coil domain-containing protein 34
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CCDC34 as an antibody target. Whether an autoantibody or antibody against CCDC34 could matter depends on whether native CCDC34 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCDC34 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 CCDC34 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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