DNLZ
DNL-type zinc finger protein
Also known as: bA413M3.2, C9orf151, DNLZ_HUMAN, HEP, RP11-413M3.2, TIMM15, ZIM17
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5SXM8
- Gene
- DNLZ
- Ensembl
- ENSG00000213221
- Chromosome
- 9
- Canonical length
- 178 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Mitochondria
OverviewNCBI Gene
Enables protein folding chaperone. Involved in chaperone-mediated protein complex assembly. Located in nucleoplasm. Is active in cytosol; mitochondrion; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
178 residues, UniProt reviewed canonical sequence.
>Q5SXM8|DNLZ
1 MLRTALRGAP RLLSRVQPRA PCLRRLWGRG ARPEVAGRRR AWAWGWRRSS SEQGPGPAAA
61 LGRVEAAHYQ LVYTCKVCGT RSSKRISKLA YHQGVVIVTC PGCQNHHIIA DNLGWFSDLN
121 GKRNIEEILT ARGEQVHRVA GEGALELVLE AAGAPTSTAA PEAGEDEGPP SPGKTEPSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DNLZ 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)
- 0.59
- Highest tissue expression
- 6.5 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 6.5 nTPM
- pancreas: 5.2 nTPM
- skeletal muscle: 3.9 nTPM
- amygdala: 3.6 nTPM
- kidney: 3.6 nTPM
- blood vessel: 3.5 nTPM
Single-cell type
- epididymal principal cells: 12 nCPM
- adrenal medulla cells: 11 nCPM
- epididymal clear cells: 6.1 nCPM
- respiratory ionocytes: 5.1 nCPM
- fallopian secretory cells: 4.8 nCPM
- epididymal efferent duct absorptive cells: 4 nCPM
Immune cell
- memory B-cell: 1.3 nTPM
- T-reg: 0.8 nTPM
- basophil: 0.7 nTPM
- MAIT T-cell: 0.7 nTPM
- memory CD8 T-cell: 0.7 nTPM
- memory CD4 T-cell: 0.6 nTPM
Brain region
- cerebellum: 4.2 nTPM
- white matter: 4 nTPM
- basal ganglia: 3.8 nTPM
- pons: 3.7 nTPM
- thalamus: 3.5 nTPM
- cerebral cortex: 3.4 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)
- 1.87
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.87
- DepMap mean gene effect
- -0.43
- 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
- chaperone-mediated protein complex assembly
- protein folding
- protein import into mitochondrial matrix
- protein stabilization
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, DNL-type
- Mitochondrial import protein TIM15
- DNL zinc finger
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DNLZ 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 DNLZ as an antibody target. Whether an autoantibody or antibody against DNLZ could matter depends on whether native DNLZ is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DNLZ 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 DNLZ as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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