FIZ1
Flt3-interacting zinc finger protein 1
Also known as: FIZ1_HUMAN, FLJ14768, ZNF798
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96SL8
- Gene
- FIZ1
- Ensembl
- ENSG00000179943
- Chromosome
- 19
- Canonical length
- 496 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes zinc finger protein, which interacts with a receptor tyrosine kinase involved in the regulation of hematopoietic and lymphoid cells. This gene product also interacts with a transcription factor that regulates the expression of rod-specific genes in retina. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
496 residues, UniProt reviewed canonical sequence.
>Q96SL8|FIZ1
1 MDDVPAPTPA PAPPAAAAPR VPFHCSECGK SFRYRSDLRR HFARHTALKP HACPRCGKGF
61 KHSFNLANHL RSHTGERPYR CSACPKGFRD STGLLHHQVV HTGEKPYCCL VCELRFSSRS
121 SLGRHLKRQH RGVLPSPLQP GPGLPALSAP CSVCCNVGPC SVCGGSGAGG GEGPEGAGAG
181 LGSWGLAEAA AAAAASLPPF ACGACARRFD HGRELAAHWA AHTDVKPFKC PRCERDFNAP
241 ALLERHKLTH DLQGPGAPPA QAWAAGPGAG PETAGEGTAA EAGDAPLASD RRLLLGPAGG
301 GVPKLGGLLP EGGGEAPAPA AAAEPSEDTL YQCDCGTFFA SAAALASHLE AHSGPATYGC
361 GHCGALYAAL AALEEHRRVS HGEGGGEEAA TAAREREPAS GEPPSGSGRG KKIFGCSECE
421 KLFRSPRDLE RHVLVHTGEK PFPCLECGKF FRHECYLKRH RLLHGTERPF PCHICGKGFI
481 TLSNLSRHLK LHRGMDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FIZ1 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)
- 0.51
- Highest tissue expression
- 18 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 18 nTPM
- cerebellum: 17 nTPM
- basal ganglia: 16 nTPM
- midbrain: 15 nTPM
- spinal cord: 14 nTPM
- hippocampal formation: 14 nTPM
Single-cell type
- adrenal medulla cells: 21 nCPM
- cardiomyocytes: 19 nCPM
- adipocytes: 14 nCPM
- retinal pigment epithelial cells: 13 nCPM
- gastric progenitor cells: 12 nCPM
- thymic myoid cells: 11 nCPM
Immune cell
- plasmacytoid DC: 0.9 nTPM
- intermediate monocyte: 0.7 nTPM
- memory B-cell: 0.6 nTPM
- memory CD4 T-cell: 0.6 nTPM
- NK-cell: 0.5 nTPM
- classical monocyte: 0.4 nTPM
Brain region
- cerebral cortex: 29 nTPM
- thalamus: 29 nTPM
- basal ganglia: 27 nTPM
- amygdala: 27 nTPM
- midbrain: 25 nTPM
- medulla oblongata: 25 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)
- 0.59
- gnomAD pLI
- 0.53
- gnomAD missense Z
- 3.5
- DepMap mean gene effect
- 0.12
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- receptor tyrosine kinase binding
- RNA polymerase II-specific DNA-binding transcription factor binding
- transcription coactivator activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FIZ1 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 FIZ1 as an antibody target. Whether an autoantibody or antibody against FIZ1 could matter depends on whether native FIZ1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FIZ1 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 FIZ1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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