HSF5
Heat shock factor protein 5
Also known as: FLJ40311, HSF5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q4G112
- Gene
- HSF5
- Ensembl
- ENSG00000176160
- Chromosome
- 17
- Canonical length
- 596 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in several processes, including male meiotic nuclear division; regulation of DNA-templated transcription; and spermatogenesis. Predicted to be located in XY body and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
596 residues, UniProt reviewed canonical sequence.
>Q4G112|HSF5
1 MEALLSTPIN PNNFPAKLWR LVNSPRYRSI RWDGRGEGLL IDQPLFEAEL LSPPGPGGGG
61 GTAGAGAEPE LFKTTSFTSF IRQLNLYGFR KVVLGGPGGG KPAGNGPLHH FHNPHFRRDQ
121 PQLLVHLKRL TSANKAKLAA GLEVPCRPPN RFQRLLITSA SAATAPLQHQ QPPPPAGPRP
181 EPHGPVAVGQ FHRSFRRDSL SPYSCVSTPS HDHSTYPLKG LDRTPVPHRI WQNSLGMHPG
241 QVETSPTFSD KGVPFPVLQR FPTEVTYTLQ PSTTSVHVQQ GPQTMVSSSQ KYSNYTPSAQ
301 YSQAYYPTAV LQCCSPTHMD ALSSCVTPTA SSYAHCNYFQ NPSMQSSYPV EFLPSNWPCS
361 TTDENTKTEV NLEAVFQIVD ELHSSPKLEM VKVEPVENQC PTSPSYRGQH ILANSNNSNP
421 CSASQASQLE PLTPVGSDIM SFVVGTEQAV ACSLPQSPEY IYTIHTAQPV ENSTIQESAA
481 IQQAHVKLKE HLNHNPSPSS VVFVQEGPPF STHQVDANIK CQTSSRENIL PSEQMGFLIS
541 EMGPASKPSE DTGLATPARY REHRSNSQQG KSPDLHLLVD VACKQERFPK EEELKELocalizationUniProt · AlphaFold · HPA
Whether an antibody against HSF5 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)
- 0.64
- Highest tissue expression
- 46 nTPM
Expression across tissuesHPA
Tissue
- testis: 46 nTPM
- lymph node: 1.1 nTPM
- thymus: 0.8 nTPM
- tonsil: 0.8 nTPM
- appendix: 0.4 nTPM
- bone marrow: 0.4 nTPM
Single-cell type
- late primary spermatocytes: 135 nCPM
- early primary spermatocytes: 50 nCPM
- early spermatids: 36 nCPM
- retinal ganglion cells: 27 nCPM
- pdcs: 27 nCPM
- hematopoietic stem cells: 25 nCPM
Immune cell
- naive B-cell: 1.3 nTPM
- memory B-cell: 1.1 nTPM
- naive CD4 T-cell: 1.1 nTPM
- T-reg: 0.9 nTPM
- naive CD8 T-cell: 0.8 nTPM
- memory CD4 T-cell: 0.6 nTPM
Brain region
- cerebellum: 0.9 nTPM
- pons: 0.5 nTPM
- cerebral cortex: 0.4 nTPM
- medulla oblongata: 0.4 nTPM
- white matter: 0.4 nTPM
- amygdala: 0.3 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)
- 0.3
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 2.6
- DepMap mean gene effect
- -0.19
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- DNA-binding transcription activator activity
- DNA-binding transcription repressor activity
- sequence-specific double-stranded DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HSF5 as an antibody target. Whether an autoantibody or antibody against HSF5 could matter depends on whether native HSF5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HSF5 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 HSF5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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