ADTRP
Androgen-dependent TFPI-regulating protein
Also known as: ADTRP_HUMAN, AIG1L, C6orf105, dJ413H6.1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96IZ2
- Gene
- ADTRP
- Ensembl
- ENSG00000111863
- Chromosome
- 6
- Canonical length
- 230 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Nucleoli
OverviewNCBI Gene
Enables hydrolase activity. Involved in several processes, including cell migration involved in sprouting angiogenesis; cellular response to oxidised low-density lipoprotein particle stimulus; and negative regulation of secretion by cell. Located in caveola and cell surface. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
230 residues, UniProt reviewed canonical sequence.
>Q96IZ2|ADTRP
1 MTKTSTCIYH FLVLSWYTFL NYYISQEGKD EVKPKILANG ARWKYMTLLN LLLQTIFYGV
61 TCLDDVLKRT KGGKDIKFLT AFRDLLFTTL AFPVSTFVFL AFWILFLYNR DLIYPKVLDT
121 VIPVWLNHAM HTFIFPITLA EVVLRPHSYP SKKTGLTLLA AASIAYISRI LWLYFETGTW
181 VYPVFAKLSL LGLAAFFSLS YVFIASIYLL GEKLNHWKWG DMRQPRKKRKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ADTRP 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
- 6
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 98 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 98 nTPM
- small intestine: 93 nTPM
- parathyroid gland: 87 nTPM
- duodenum: 78 nTPM
- colon: 76 nTPM
- rectum: 55 nTPM
Single-cell type
- late spermatids: 372 nCPM
- retinal pigment epithelial cells: 311 nCPM
- renal collecting duct intercalated cells: 209 nCPM
- enterocytes: 199 nCPM
- early spermatids: 196 nCPM
- foveolar cells: 166 nCPM
Immune cell
- naive CD4 T-cell: 15 nTPM
- T-reg: 14 nTPM
- memory CD4 T-cell: 3.7 nTPM
- basophil: 2.8 nTPM
- MAIT T-cell: 2.6 nTPM
- total PBMC: 1.8 nTPM
Brain region
- choroid plexus: 79 nTPM
- cerebral cortex: 8.2 nTPM
- basal ganglia: 7.6 nTPM
- hippocampal formation: 6.9 nTPM
- white matter: 6.1 nTPM
- cerebellum: 5 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)
- 1.37
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.18
- DepMap mean gene effect
- 0.14
- 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
- cell migration involved in sprouting angiogenesis
- cellular response to oxidised low-density lipoprotein particle stimulus
- cellular response to steroid hormone stimulus
- long-chain fatty acid catabolic process
- negative regulation of blood coagulation
- negative regulation of extracellular matrix constituent secretion
- negative regulation of leukocyte cell-cell adhesion
- negative regulation of leukocyte migration
- negative regulation of lymphocyte migration
- negative regulation of protein secretion
- positive regulation of gene expression
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ADTRP as an antibody target. Whether an autoantibody or antibody against ADTRP could matter depends on whether native ADTRP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ADTRP is annotated at the cell surface, where native ADTRP 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 ADTRP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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