Entity Details

Primary name HSF4_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9ULV5
EntryNameHSF4_HUMAN
FullNameHeat shock factor protein 4
TaxID9606
Evidenceevidence at protein level
Length492
SequenceStatuscomplete
DateCreated2001-01-11
DateModified2021-06-02

Ontological Relatives

GenesHSF4

GO terms

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GOName
GO:0000122 negative regulation of transcription by RNA polymerase II
GO:0000785 chromatin
GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding
GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific
GO:0003700 DNA-binding transcription factor activity
GO:0005634 nucleus
GO:0006357 regulation of transcription by RNA polymerase II
GO:0007601 visual perception
GO:0008284 positive regulation of cell population proliferation
GO:0016607 nuclear speck
GO:0019903 protein phosphatase binding
GO:0033169 histone H3-K9 demethylation
GO:0042802 identical protein binding
GO:0043010 camera-type eye development
GO:0045597 positive regulation of cell differentiation
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0048468 cell development
GO:1990837 sequence-specific double-stranded DNA binding

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR000232 Heat shock factor (HSF)-type, DNA-bindingDomainDomain
IPR027725 Heat shock transcription factor familyFamilyFamily
IPR036388 Winged helix-like DNA-binding domain superfamilyFamilyHomologous superfamily
IPR036390 Winged helix DNA-binding domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
116800 OMIMCataract 5, multiple types (CTRCT5)An opacification of the crystalline lens of the eye that frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. CTRCT5 includes infantile, lamellar, zonular, nuclear, anterior polar, stellate, and Marner-type cataracts, among others. Finger malformation is observed in some kindreds. The disease is caused by variants affecting the gene represented in this entry.

Interactions

45 interactions

InteractorPartnerSourcesPublicationsLink
HSF4_HUMANCDKA2_HUMANBioGRID, MINT21900206 details
HSF4_HUMANZBED8_HUMANBioGRID, MINT21900206 details
HSF4_HUMANCPSF5_HUMANBioGRID, MINT21900206 details
HSF4_HUMANSESD1_HUMANBioGRID, IntAct25036637 32296183 details
HSF4_HUMANYTHD1_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANK1H1_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANLIPB2_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANK1C40_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANSOX10_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANNUP62_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANPA2GX_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANAKP8L_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANFOXH1_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANFOXI1_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANKR197_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANHGS_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANTPM3_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANKRT38_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANKRT37_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANPIHD2_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANGFOD1_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANMKRN3_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANUFSP1_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANPITX1_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANKRA62_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANF168B_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANINT11_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANMS18B_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANKR196_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANCJ055_HUMANIntAct32296183 details
HSF4_HUMANNHLC4_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANKRA31_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANCS054_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANZMY12_HUMANBioGRID, IntAct32296183 details
HSF4_HUMANALKB4_HUMANBioGRID, IntAct23145062 details
HSF4_HUMANSMCA4_HUMANBioGRID16552721 details
HSF4_HUMANDUS26_HUMANBioGRID, HPRD16581800 details
HSF4_HUMANMK01_HUMANBioGRID, HPRD16581800 details
HSF4_HUMANDAXX_HUMANBioGRID20620219 details
HSF4_HUMANHSF2_HUMANBioGRID, IntAct21258402 25036637 details
HSF4_HUMANHSF4_HUMANHPRD10488131 details
HSF4_HUMANS27A5_HUMANHPRD16552721 details
HSF4_HUMANMK08_HUMANHPRD16581800 details
HSF4_HUMANMK14_HUMANHPRD16581800 details
HSF4_HUMANMK03_HUMANHPRD16581800 details