RNF32-DT
Putative transmembrane protein RNF32-DT
Also known as: R32DT_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for RNF32-DT in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
216 residues, UniProt reviewed canonical sequence.
>Q8NI28|RNF32-DT
1 MLASPARPTL RMLANHALST PHCACSPAPA PRTASASRRR CVPVEARAAG VFGDRLAGVF
61 GSRGLKHGGV QAPRPRVVRA EPRAGFAVVR SPRRLCGRSH APQPPAHLGL GPGCFPAVAV
121 VVPVPGSRAH RPFAALLVEG SFLGDPPIPP RRSGVLARGS AGADCLASSV TPGPSLWIPL
181 LLVAGCVSCF VGLAVCVWMQ ARVSPAWPAG LFLLPRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RNF32-DT 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
- 1
- Mean surface accessibility (rSASA)
- 0.63
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Cellular components
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RNF32-DT as an antibody target. Whether an autoantibody or antibody against RNF32-DT could matter depends on whether native RNF32-DT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RNF32-DT 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 RNF32-DT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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