IGFBPL1
Insulin-like growth factor-binding protein-like 1
Also known as: bA113O24.1, IBPL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WX77
- Gene
- IGFBPL1
- Ensembl
- ENSG00000137142
- Chromosome
- 9
- Canonical length
- 278 aa
- Protein class
- Predicted secreted proteins
- Subcellular location
- Nucleoplasm,Vesicles
- Secretome location
- Secreted to blood
OverviewNCBI Gene
Predicted to enable insulin-like growth factor binding activity. Involved in cellular response to tumor cell. Located in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
278 residues, UniProt reviewed canonical sequence.
>Q8WX77|IGFBPL1
1 MPRLSLLLPL LLLLLLPLLP PLSPSLGIRD VGGRRPKCGP CRPEGCPAPA PCPAPGISAL
61 DECGCCARCL GAEGASCGGR AGGRCGPGLV CASQAAGAAP EGTGLCVCAQ RGTVCGSDGR
121 SYPSVCALRL RARHTPRAHP GHLHKARDGP CEFAPVVVVP PRSVHNVTGA QVGLSCEVRA
181 VPTPVITWRK VTKSPEGTQA LEELPGDHVN IAVQVRGGPS DHEATAWILI NPLRKEDEGV
241 YQCHAANMVG EAESHSTVTV LDLSKYRSFH FPAPDDRMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IGFBPL1 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)
- 0.41
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 16 nTPM
- blood vessel: 7.8 nTPM
- basal ganglia: 5.4 nTPM
- cerebellum: 3.9 nTPM
- pituitary gland: 3.4 nTPM
- thymus: 2.7 nTPM
Single-cell type
- early spermatids: 25 nCPM
- adrenal medulla cells: 21 nCPM
- late spermatids: 21 nCPM
- pancreatic islet cells: 21 nCPM
- somatotrophs: 17 nCPM
- hofbauer cells: 16 nCPM
Immune cell
- basophil: 0.5 nTPM
- neutrophil: 0.4 nTPM
- gdT-cell: 0.2 nTPM
- naive B-cell: 0.2 nTPM
- NK-cell: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
Brain region
- basal ganglia: 11 nTPM
- cerebellum: 9.1 nTPM
- hypothalamus: 8.1 nTPM
- hippocampal formation: 7.6 nTPM
- midbrain: 7.4 nTPM
- cerebral cortex: 6.9 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)
- 1.64
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.44
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Insulin-like growth factor-binding protein, IGFBP
- Kazal domain
- Immunoglobulin subtype 2
- Immunoglobulin domain subtype
- Immunoglobulin-like domain
- Growth factor receptor cysteine-rich domain superfamily
- Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25
- Immunoglobulin I-set
- Immunoglobulin-like fold
- Kazal domain superfamily
- Immunoglobulin-like domain superfamily
- Insulin-like growth factor binding protein
- Kazal-type serine protease inhibitor domain
- Immunoglobulin I-set domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IGFBPL1 as an antibody target. Whether an autoantibody or antibody against IGFBPL1 could matter depends on whether native IGFBPL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IGFBPL1 is annotated as secreted, so native IGFBPL1 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 IGFBPL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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