ABHD17B
Alpha/beta hydrolase domain-containing protein 17B
Also known as: AB17B_HUMAN, C9orf77, CGI-67, FAM108B1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5VST6
- Gene
- ABHD17B
- Ensembl
- ENSG00000107362
- Chromosome
- 9
- Canonical length
- 288 aa
- Protein class
- Enzymes, Predicted intracellular proteins
OverviewNCBI Gene
Enables palmitoyl-(protein) hydrolase activity. Involved in protein depalmitoylation. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
288 residues, UniProt reviewed canonical sequence.
>Q5VST6|ABHD17B
1 MNNLSFSELC CLFCCPPCPG KIASKLAFLP PDPTYTLMCD ESGSRWTLHL SERADWQYSS
61 REKDAIECFM TRTSKGNRIA CMFVRCSPNA KYTLLFSHGN AVDLGQMSSF YIGLGSRINC
121 NIFSYDYSGY GASSGKPTEK NLYADIEAAW LALRTRYGIR PENVIIYGQS IGTVPSVDLA
181 ARYESAAVIL HSPLTSGMRV AFPDTKKTYC FDAFPNIDKI SKITSPVLII HGTEDEVIDF
241 SHGLALFERC QRPVEPLWVE GAGHNDVELY GQYLERLKQF VSQELVNLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ABHD17B 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 31 nTPM
Expression across tissuesHPA
Tissue
- thymus: 31 nTPM
- spinal cord: 26 nTPM
- retina: 24 nTPM
- hippocampal formation: 19 nTPM
- bone marrow: 18 nTPM
- cerebral cortex: 17 nTPM
Single-cell type
- rod photoreceptor cells: 435 nCPM
- oligodendrocytes: 208 nCPM
- urothelial cells: 198 nCPM
- lymphatic endothelial cells: 163 nCPM
- colonocytes: 157 nCPM
- innate lymphoid cells: 155 nCPM
Immune cell
- naive B-cell: 4.2 nTPM
- basophil: 3.6 nTPM
- NK-cell: 3.3 nTPM
- plasmacytoid DC: 2.6 nTPM
- T-reg: 2.5 nTPM
- myeloid DC: 2.2 nTPM
Brain region
- white matter: 87 nTPM
- basal ganglia: 54 nTPM
- cerebral cortex: 45 nTPM
- midbrain: 43 nTPM
- spinal cord: 42 nTPM
- medulla oblongata: 42 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ABHD17B.
Disease | ImmuneIEDB
Conditions an epitope on ABHD17B was assayed in.
- melanoma T cell
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)
- 0.65
- gnomAD pLI
- 0.25
- gnomAD missense Z
- 2.62
- DepMap mean gene effect
- -0.01
- 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).
OntologyGO
Biological processes
- negative regulation of protein localization to microtubule
- positive regulation of protein localization to endosome
- protein depalmitoylation
- regulation of dendritic spine maintenance
- regulation of postsynapse organization
- regulation of protein localization to synapse
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ABHD17B as an antibody target. Whether an autoantibody or antibody against ABHD17B could matter depends on whether native ABHD17B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ABHD17B is annotated at the cell surface, where native ABHD17B is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ABHD17B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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