CRABP2
Cellular retinoic acid-binding protein 2
Also known as: CRABP-II, RABP2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P29373
- Gene
- CRABP2
- Ensembl
- ENSG00000143320
- Chromosome
- 1
- Canonical length
- 138 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene encodes a member of the retinoic acid (RA, a form of vitamin A) binding protein family and lipocalin/cytosolic fatty-acid binding protein family. The protein is a cytosol-to-nuclear shuttling protein, which facilitates RA binding to its cognate receptor complex and transfer to the nucleus. It is involved in the retinoid signaling pathway, and is associated with increased circulating low-density lipoprotein cholesterol. Alternatively spliced transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2010]
Canonical amino-acid sequenceUniProt
138 residues, UniProt reviewed canonical sequence.
>P29373|CRABP2
1 MPNFSGNWKI IRSENFEELL KVLGVNVMLR KIAVAAASKP AVEIKQEGDT FYIKTSTTVR
61 TTEINFKVGE EFEEQTVDGR PCKSLVKWES ENKMVCEQKL LKGEGPKTSW TRELTNDGEL
121 ILTMTADDVV CTRVYVRELocalizationUniProt · AlphaFold · HPA
Whether an antibody against CRABP2 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
- 1,174 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 1,174 nTPM
- vagina: 590 nTPM
- cervix: 567 nTPM
- skin: 174 nTPM
- choroid plexus: 152 nTPM
- breast: 98 nTPM
Single-cell type
- esophageal suprabasal cells: 4,577 nCPM
- esophageal basal cells: 1,651 nCPM
- esophageal apical cells: 1,358 nCPM
- breast secretory cells: 611 nCPM
- prostatic club cells: 420 nCPM
- epididymal basal cells: 338 nCPM
Immune cell
- memory CD4 T-cell: 0.1 nTPM
- naive CD4 T-cell: 0.1 nTPM
- naive CD8 T-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- choroid plexus: 55 nTPM
- cerebral cortex: 34 nTPM
- hypothalamus: 18 nTPM
- basal ganglia: 15 nTPM
- hippocampal formation: 14 nTPM
- cerebellum: 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)
- 1.44
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.22
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- embryonic forelimb morphogenesis
- epidermis development
- fatty acid transport
- positive regulation of collateral sprouting
- regulation of DNA-templated transcription
- retinoic acid metabolic process
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CRABP2 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 CRABP2 as an antibody target. Whether an autoantibody or antibody against CRABP2 could matter depends on whether native CRABP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CRABP2 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 CRABP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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