PHF13
PHD finger protein 13
Also known as: MGC43399, PHF13_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86YI8
- Gene
- PHF13
- Ensembl
- ENSG00000116273
- Chromosome
- 1
- Canonical length
- 300 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables chromatin binding activity; chromatin-protein adaptor activity; and methylated histone binding activity. Involved in mitotic chromosome condensation and regulation of DNA repair. Located in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
300 residues, UniProt reviewed canonical sequence.
>Q86YI8|PHF13
1 MDSDSCAAAF HPEEYSPSCK RRRTVEDFNK FCTFVLAYAG YIPYPKEELP LRSSPSPANS
61 TAGTIDSDGW DAGFSDIASS VPLPVSDRCF SHLQPTLLQR AKPSNFLLDR KKTDKLKKKK
121 KRKRRDSDAP GKEGYRGGLL KLEAADPYVE TPTSPTLQDI PQAPSDPCSG WDSDTPSSGS
181 CATVSPDQVK EIKTEGKRTI VRQGKQVVFR DEDSTGNDED IMVDSDDDSW DLVTCFCMKP
241 FAGRPMIECN ECHTWIHLSC AKIRKSNVPE VFVCQKCRDS KFDIRRSNRS RTGSRKLFLDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PHF13 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)
- 0.63
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- testis: 33 nTPM
- cervix: 19 nTPM
- blood vessel: 19 nTPM
- colon: 16 nTPM
- endometrium: 16 nTPM
- esophagus: 15 nTPM
Single-cell type
- undifferentiated spermatogonia: 53 nCPM
- esophageal apical cells: 45 nCPM
- differentiating spermatogonia: 40 nCPM
- syncytiotrophoblasts: 37 nCPM
- ocular epithelial cells: 36 nCPM
- suprabasal keratinocytes: 35 nCPM
Immune cell
- eosinophil: 4.6 nTPM
- neutrophil: 4.1 nTPM
- MAIT T-cell: 3.6 nTPM
- memory CD4 T-cell: 3 nTPM
- NK-cell: 2.8 nTPM
- T-reg: 2.5 nTPM
Brain region
- hypothalamus: 14 nTPM
- white matter: 13 nTPM
- medulla oblongata: 12 nTPM
- cerebral cortex: 12 nTPM
- midbrain: 11 nTPM
- hippocampal formation: 11 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)
- 0.25
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 1.76
- DepMap mean gene effect
- -0.07
- 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
Biological processes
- cell division
- chromosome segregation
- DNA damage response
- mitotic cell cycle
- mitotic chromosome condensation
Molecular functions
- chromatin binding
- chromatin-protein adaptor activity
- histone H3K9me2/3 reader activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PHF13 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 PHF13 as an antibody target. Whether an autoantibody or antibody against PHF13 could matter depends on whether native PHF13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PHF13 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 PHF13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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