C8orf17
Protein MOST-1
Also known as: MOST1_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for C8orf17 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
99 residues, UniProt reviewed canonical sequence.
>Q9NRJ1|C8orf17
1 MGECPHLVDV RLGHRSLATG PEQSDICHTG SEARWTTTWY GSLSFSRHKY KMLADLTPGV
61 EMSCRHWARW LTPVIPALWK AEAGGLPELR SSRPAWTTWLocalizationUniProt · AlphaFold · HPA
Whether an antibody against C8orf17 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.65
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 missense Z
- -0.22
OntologyGO
Biological processes
Cellular components
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of C8orf17 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 C8orf17 as an antibody target. Whether an autoantibody or antibody against C8orf17 could matter depends on whether native C8orf17 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
C8orf17 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 C8orf17 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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