GLTPD2
Glycolipid transfer protein domain-containing protein 2
Also known as: GLTD2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NH11
- Gene
- GLTPD2
- Ensembl
- ENSG00000182327
- Chromosome
- 17
- Canonical length
- 291 aa
- Protein class
- Predicted secreted proteins
- Subcellular location
- Nucleoplasm,Vesicles
- Secretome location
- Secreted - unknown location
OverviewNCBI Gene
Predicted to enable ceramide 1-phosphate binding activity and ceramide 1-phosphate transfer activity. Predicted to be involved in ceramide transport and intermembrane lipid transfer. Predicted to be located in cytoplasm. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
291 residues, UniProt reviewed canonical sequence.
>A6NH11|GLTPD2
1 MGVAARPPAL RHWFSHSIPL AIFALLLLYL SVRSLGARSG CGPRAQPCVP GETAPFQVRQ
61 ESGTLEAPER KQPPCLGPRG MLGRMMRRFH ASLKPEGDVG LSPYLAGWRA LVEFLTPLGS
121 VFAFATREAF TKVTDLEARV HGPDAEHYWS LVAMAAWERR AGLLEQPGAA PRDPTRSSGS
181 RTLLLLHRAL RWSQLCLHRV ATGALGGPDA GVQCSDAYRA ALGPHHPWLV RQTARLAFLA
241 FPGRRRLLEL ACPGATEAEA RAALVRAAGT LEDVYNRTQS LLAERGLLQL ALocalizationUniProt · AlphaFold · HPA
Whether an antibody against GLTPD2 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)
- 0.36
- Highest tissue expression
- 75 nTPM
Expression across tissuesHPA
Tissue
- liver: 75 nTPM
- kidney: 12 nTPM
- duodenum: 9.5 nTPM
- small intestine: 5.8 nTPM
- cerebral cortex: 1.9 nTPM
- skin: 1.6 nTPM
Single-cell type
- hepatocytes: 169 nCPM
- enterocytes: 56 nCPM
- epicardial cells: 18 nCPM
- epididymal efferent duct absorptive cells: 16 nCPM
- gastric progenitor cells: 12 nCPM
- neuroendocrine cells: 8.6 nCPM
Immune cell
- non-classical monocyte: 0.6 nTPM
- intermediate monocyte: 0.1 nTPM
- myeloid DC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- midbrain: 15 nTPM
- medulla oblongata: 15 nTPM
- cerebral cortex: 14 nTPM
- cerebellum: 13 nTPM
- pons: 13 nTPM
- hypothalamus: 13 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)
- 1.54
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.16
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- none
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GLTPD2 as an antibody target. Whether an autoantibody or antibody against GLTPD2 could matter depends on whether native GLTPD2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GLTPD2 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 GLTPD2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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