ADISSP
Adipose-secreted signaling protein
Also known as: ADSSP_HUMAN, C20orf27, FLJ20550
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9GZN8
- Gene
- ADISSP
- Ensembl
- ENSG00000101220
- Chromosome
- 20
- Canonical length
- 174 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
Enables protein phosphatase 1 binding activity. Involved in positive regulation of non-canonical NF-kappaB signal transduction and positive regulation of transforming growth factor beta receptor signaling pathway. Predicted to be located in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
174 residues, UniProt reviewed canonical sequence.
>Q9GZN8|ADISSP
1 MAAANKGNKP RVRSIRFAAG HDAEGSHSHV HFDEKLHDSV VMVTQESDSS FLVKVGFLKI
61 LHRYEITFTL PPVHRLSKDV REAPVPSLHL KLLSVVPVPE GYSVKCEYSA HKEGVLKEEI
121 LLACEGGTGT CVRVTVQARV MDRHHGTPML LDGVKCVGAE LEYDSEHSDW HGFDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ADISSP 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.43
- Highest tissue expression
- 319 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 319 nTPM
- colon: 131 nTPM
- bone marrow: 98 nTPM
- stomach: 95 nTPM
- urinary bladder: 86 nTPM
- ovary: 74 nTPM
Single-cell type
- decidual stromal cells: 786 nCPM
- hofbauer cells: 205 nCPM
- monocyte progenitors: 151 nCPM
- smooth muscle cells: 145 nCPM
- ovarian stromal cells: 129 nCPM
- endometrial stromal cells: 125 nCPM
Immune cell
- intermediate monocyte: 249 nTPM
- non-classical monocyte: 236 nTPM
- myeloid DC: 200 nTPM
- classical monocyte: 145 nTPM
- total PBMC: 87 nTPM
- MAIT T-cell: 42 nTPM
Brain region
- basal ganglia: 213 nTPM
- pons: 94 nTPM
- hypothalamus: 84 nTPM
- midbrain: 77 nTPM
- thalamus: 75 nTPM
- medulla oblongata: 61 nTPM
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)
- 1.29
- gnomAD pLI
- 0.01
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adaptive thermogenesis
- glucose homeostasis
- positive regulation of non-canonical NF-kappaB signal transduction
- positive regulation of protein kinase A signaling
- positive regulation of transforming growth factor beta receptor signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Adipose-secreted signaling protein
- Domain of unknown function (DUF4517)
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ADISSP 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 ADISSP as an antibody target. Whether an autoantibody or antibody against ADISSP could matter depends on whether native ADISSP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ADISSP is annotated as secreted, so native ADISSP circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label ADISSP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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