ZAR1L
Protein ZAR1-like
Also known as: Z3CXXC7, ZAR1L_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NP61
- Gene
- ZAR1L
- Ensembl
- ENSG00000189167
- Chromosome
- 13
- Canonical length
- 321 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear speckles
OverviewNCBI Gene
This gene encodes a member of the ZAR1 family that is predominantly expressed in oocytes and early embryos. The protein may function as an RNA regulator in early embryos. [provided by RefSeq, Apr 2010]
Canonical amino-acid sequenceUniProt
321 residues, UniProt reviewed canonical sequence.
>A6NP61|ZAR1L
1 MERFVRVPYG LYQGYGSTVP LGQPGLSGHK QPDWRQNMGP PTFLARPGLL VPANAPDYCI
61 DPYKRAQLKA ILSQMNPSLS PRLCKPNTKE VGVQVSPRVD KAVQCSLGPR TLSSCSPWDG
121 RDPQEPLPAC GVTSPATGRR GLIRLRRDGD EAESKALPGP AEASQPQPPS RRSGADRQEE
181 PGQLEESGEK DAPCPQETKS KQVPGDAASE PLRRPNFQFL EPKYGYFHCK DCKTRWESAY
241 VWCISGTNKV YFKQLCCKCQ KSFNPYRVEA IQCQTCSKSH CSCPQKKRHI DLRRPHRQEL
301 CGRCKDKRFS CGNIYSFKYV MLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZAR1L 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)
- 0.56
- Highest tissue expression
- 0.7 nTPM
Expression across tissuesHPA
Tissue
- testis: 0.7 nTPM
- bone marrow: 0.1 nTPM
- lymph node: 0.1 nTPM
- ovary: 0.1 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
Single-cell type
- oocytes: 55 nCPM
- paneth cells: 3.9 nCPM
- cdc: 2.5 nCPM
- late primary spermatocytes: 2.5 nCPM
- undifferentiated spermatogonia: 2.5 nCPM
- early primary spermatocytes: 2.2 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- basal ganglia: 0.1 nTPM
- cerebellum: 0.1 nTPM
- cerebral cortex: 0.1 nTPM
- hippocampal formation: 0.1 nTPM
- hypothalamus: 0.1 nTPM
- midbrain: 0.1 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)
- 0.69
- gnomAD pLI
- 0.1
- gnomAD missense Z
- 1.69
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
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
InteractionsUniProt · HPA
Protein binding partners of ZAR1L 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 ZAR1L as an antibody target. Whether an autoantibody or antibody against ZAR1L could matter depends on whether native ZAR1L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZAR1L 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 ZAR1L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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