CRYZL1
Quinone oxidoreductase-like protein 1
Also known as: 4P11, QOH-1, QORL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95825
- Gene
- CRYZL1
- Ensembl
- ENSG00000205758
- Chromosome
- 21
- Canonical length
- 349 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protein that has sequence similarity to zeta crystallin, also known as quinone oxidoreductase. This zeta crystallin-like protein also contains an NAD(P)H binding site. Alternatively spliced transcript variants have been observed but their full-length nature has not been completely determined. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
349 residues, UniProt reviewed canonical sequence.
>O95825|CRYZL1
1 MKGLYFQQSS TDEEITFVFQ EKEDLPVTED NFVKLQVKAC ALSQINTKLL AEMKMKKDLF
61 PVGREIAGIV LDVGSKVSFF QPDDEVVGIL PLDSEDPGLC EVVRVHEHYL VHKPEKVTWT
121 EAAGSIRDGV RAYTALHYLS HLSPGKSVLI MDGASAFGTI AIQLAHHRGA KVISTACSLE
181 DKQCLERFRP PIARVIDVSN GKVHVAESCL EETGGLGVDI VLDAGVRLYS KDDEPAVKLQ
241 LLPHKHDIIT LLGVGGHWVT TEENLQLDPP DSHCLFLKGA TLAFLNDEVW NLSNVQQGKY
301 LCILKDVMEK LSTGVFRPQL DEPIPLYEAK VSMEAVQKNQ GRKKQVVQFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CRYZL1 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)
- 0.25
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 38 nTPM
- cerebral cortex: 35 nTPM
- amygdala: 34 nTPM
- midbrain: 32 nTPM
- testis: 32 nTPM
- spinal cord: 29 nTPM
Single-cell type
- late primary spermatocytes: 71 nCPM
- early spermatids: 28 nCPM
- migrating cytotrophoblasts: 15 nCPM
- cytotrophoblasts: 15 nCPM
- gastric chief cells: 14 nCPM
- parietal cells: 12 nCPM
Immune cell
- NK-cell: 47 nTPM
- myeloid DC: 43 nTPM
- naive CD4 T-cell: 43 nTPM
- naive B-cell: 40 nTPM
- memory B-cell: 38 nTPM
- intermediate monocyte: 38 nTPM
Brain region
- white matter: 80 nTPM
- cerebellum: 79 nTPM
- midbrain: 72 nTPM
- hypothalamus: 69 nTPM
- basal ganglia: 68 nTPM
- cerebral cortex: 68 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
- 0.76
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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 CRYZL1 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 CRYZL1 as an antibody target. Whether an autoantibody or antibody against CRYZL1 could matter depends on whether native CRYZL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CRYZL1 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 CRYZL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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