LGALS12
Galectin-12
Also known as: GRIP1, LEG12_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96DT0
- Gene
- LGALS12
- Ensembl
- ENSG00000133317
- Chromosome
- 11
- Canonical length
- 336 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a member of the galectin superfamily, a group of beta-galactoside-binding proteins with conserved carbohydrate recognition domains. The related mouse protein is a primary regulator of the early stages of adipose tissue development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, May 2010]
Canonical amino-acid sequenceUniProt
336 residues, UniProt reviewed canonical sequence.
>Q96DT0|LGALS12
1 MSQPSGGRAP GTRIYSWSCP TVMSPGEKLD PIPDSFILQP PVFHPVVPYV TTIFGGLHAG
61 KMVMLQGVVP LDAHRFQVDF QCGCSLCPRP DIAFHFNPRF HTTKPHVICN TLHGGRWQRE
121 ARWPHLALRR GSSFLILFLF GNEEVKVSVN GQHFLHFRYR LPLSHVDTLG IFGDILVEAV
181 GFLNINPFVE GSREYPAGHP FLLMSPRLEV PCSHALPQGL SPGQVIIVRG LVLQEPKHFT
241 VSLRDQAAHA PVTLRASFAD RTLAWISRWG QKKLISAPFL FYPQRFFEVL LLFQEGGLKL
301 ALNGQGLGAT SMNQQALEQL RELRISGSVQ LYCVHSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LGALS12 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)
- 0.29
- Highest tissue expression
- 74 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 74 nTPM
- breast: 40 nTPM
- bone marrow: 17 nTPM
- blood vessel: 13 nTPM
- salivary gland: 4.2 nTPM
- appendix: 2.5 nTPM
Single-cell type
- platelets: 243 nCPM
- adipocytes: 153 nCPM
- neutrophil progenitors: 34 nCPM
- mast cells: 13 nCPM
- megakaryocytes: 12 nCPM
- monocyte progenitors: 5.2 nCPM
Immune cell
- eosinophil: 556 nTPM
- classical monocyte: 28 nTPM
- total PBMC: 17 nTPM
- basophil: 16 nTPM
- myeloid DC: 7.5 nTPM
- neutrophil: 5.7 nTPM
Brain region
- choroid plexus: 0.8 nTPM
- white matter: 0.5 nTPM
- medulla oblongata: 0.4 nTPM
- amygdala: 0.3 nTPM
- basal ganglia: 0.3 nTPM
- cerebral cortex: 0.3 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)
- 1.59
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.03
- DepMap mean gene effect
- -0.02
- 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
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LGALS12 as an antibody target. Whether an autoantibody or antibody against LGALS12 could matter depends on whether native LGALS12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LGALS12 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 LGALS12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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