CRELD2
Protein disulfide isomerase CRELD2
Also known as: CREL2_HUMAN, MGC11256
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6UXH1
- Gene
- CRELD2
- Ensembl
- ENSG00000184164
- Chromosome
- 22
- Canonical length
- 353 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
Predicted to enable calcium ion binding activity and protein disulfide isomerase activity. Predicted to be located in Golgi apparatus; endoplasmic reticulum; and extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
353 residues, UniProt reviewed canonical sequence.
>Q6UXH1|CRELD2
1 MRLPRRAALG LLPLLLLLPP APEAAKKPTP CHRCRGLVDK FNQGMVDTAK KNFGGGNTAW
61 EEKTLSKYES SEIRLLEILE GLCESSDFEC NQMLEAQEEH LEAWWLQLKS EYPDLFEWFC
121 VKTLKVCCSP GTYGPDCLAC QGGSQRPCSG NGHCSGDGSR QGDGSCRCHM GYQGPLCTDC
181 MDGYFSSLRN ETHSICTACD ESCKTCSGLT NRDCGECEVG WVLDEGACVD VDECAAEPPP
241 CSAAQFCKNA NGSYTCEECD SSCVGCTGEG PGNCKECISG YAREHGQCAD VDECSLAEKT
301 CVRKNENCYN TPGSYVCVCP DGFEETEDAC VPPAEAEATE GESPTQLPSR EDLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CRELD2 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)
- 0.39
- Highest tissue expression
- 115 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 115 nTPM
- liver: 87 nTPM
- thyroid gland: 61 nTPM
- pituitary gland: 59 nTPM
- stomach: 42 nTPM
- testis: 40 nTPM
Single-cell type
- plasma cells: 364 nCPM
- epididymal principal cells: 329 nCPM
- pancreatic acinar cells: 155 nCPM
- extravillous trophoblasts: 154 nCPM
- early primary spermatocytes: 153 nCPM
- differentiating spermatogonia: 132 nCPM
Immune cell
- plasmacytoid DC: 52 nTPM
- NK-cell: 36 nTPM
- basophil: 34 nTPM
- memory B-cell: 29 nTPM
- naive B-cell: 28 nTPM
- memory CD8 T-cell: 23 nTPM
Brain region
- thalamus: 33 nTPM
- hypothalamus: 26 nTPM
- medulla oblongata: 26 nTPM
- pons: 25 nTPM
- white matter: 24 nTPM
- basal ganglia: 22 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)
- 1.05
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.42
- DepMap mean gene effect
- 0.04
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CRELD2 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 CRELD2 as an antibody target. Whether an autoantibody or antibody against CRELD2 could matter depends on whether native CRELD2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CRELD2 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 CRELD2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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