LGALS9B
Galectin-9B
Also known as: LEG9B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q3B8N2
- Gene
- LGALS9B
- Ensembl
- ENSG00000170298
- Chromosome
- 17
- Canonical length
- 356 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene was initially thought to represent a pseudogene of galectin 9; however, this transcript has good exon-intron structure and encodes a predicted protein of the same size as and highly similar to galectin 9. This gene is one of two similar loci on chromosome 17p similar to galectin 9 and now thought to be protein-encoding. This gene is the more centromeric gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
356 residues, UniProt reviewed canonical sequence.
>Q3B8N2|LGALS9B
1 MAFSGSQAPY LSPAVPFSGT IQGGLQDGFQ ITVNGAVLSS SGTRFAVDFQ TGFSGNDIAF
61 HFNPRFEDGG YVVCNTRQKG RWGPEERKMH MPFQKGMPFD LCFLVQSSDF KVMVNGSLFV
121 QYFHRVPFHR VDTISVNGSV QLSYISFQNP RTVPVQPAFS TVPFSQPVCF PPRPRGRRQK
181 PPSVRPANPA PITQTVIHTV QSASGQMFSQ TPAIPPMMYP HPAYPMPFIT TIPGGLYPSK
241 SIILSGTVLP SAQRFHINLC SGSHIAFHMN PRFDENAVVR NTQINNSWGS EERSLPRKMP
301 FVRGQSFSVW ILCEAHCLKV AVDGQHVFEY YHRLRNLPTI NKLEVGGDIQ LTHVQTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LGALS9B 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 29 nTPM
Expression across tissuesHPA
Tissue
- stomach: 29 nTPM
- esophagus: 15 nTPM
- rectum: 10 nTPM
- colon: 7.7 nTPM
- gallbladder: 7 nTPM
- vagina: 4 nTPM
Single-cell type
- foveolar cells: 220 nCPM
- goblet cells: 68 nCPM
- esophageal apical cells: 29 nCPM
- colonocytes: 19 nCPM
- respiratory secretory cells: 11 nCPM
- respiratory deuterosomal cells: 10 nCPM
Immune cell
- NK-cell: 13 nTPM
- total PBMC: 2 nTPM
- gdT-cell: 0.8 nTPM
- naive CD8 T-cell: 0.4 nTPM
- myeloid DC: 0.3 nTPM
- non-classical monocyte: 0.3 nTPM
Brain region
- hippocampal formation: 0.3 nTPM
- cerebral cortex: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
- midbrain: 0.1 nTPM
- spinal cord: 0.1 nTPM
- white matter: 0.1 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)
- 1.17
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.54
- DepMap mean gene effect
- -0.34
- 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
- negative regulation of CD4-positive, alpha-beta T cell proliferation
- negative regulation of type II interferon production
- positive regulation of gene expression
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LGALS9B 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 LGALS9B as an antibody target. Whether an autoantibody or antibody against LGALS9B could matter depends on whether native LGALS9B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LGALS9B 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 LGALS9B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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