Entity Details

Primary name T2EB_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP29084
EntryNameT2EB_HUMAN
FullNameTranscription initiation factor IIE subunit beta
TaxID9606
Evidenceevidence at protein level
Length291
SequenceStatuscomplete
DateCreated1992-12-01
DateModified2021-06-02

Ontological Relatives

GenesGTF2E2

GO terms

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GOName
GO:0003677 DNA binding
GO:0003723 RNA binding
GO:0005654 nucleoplasm
GO:0005669 transcription factor TFIID complex
GO:0005673 transcription factor TFIIE complex
GO:0005829 cytosol
GO:0006366 transcription by RNA polymerase II
GO:0006367 transcription initiation from RNA polymerase II promoter
GO:0016251 RNA polymerase II general transcription initiation factor activity
GO:0016607 nuclear speck
GO:0042795 snRNA transcription by RNA polymerase II

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR003166 Transcription factor TFIIE beta subunit, DNA-binding domainDomainDomain
IPR016656 Transcription initiation factor TFIIE, beta subunitFamilyFamily
IPR036388 Winged helix-like DNA-binding domain superfamilyFamilyHomologous superfamily
IPR036390 Winged helix DNA-binding domain superfamilyFamilyHomologous superfamily
IPR040501 TFA2, Winged helix domain 2DomainDomain

Diseases

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Disease IDSourceNameDescription
616943 OMIMTrichothiodystrophy 6, non-photosensitive (TTD6)A form of trichothiodystrophy, a disease characterized by sulfur-deficient brittle hair and multisystem variable abnormalities. The spectrum of clinical features varies from mild disease with only hair involvement to severe disease with cutaneous, neurologic and profound developmental defects. Ichthyosis, intellectual and developmental disabilities, decreased fertility, abnormal characteristics at birth, ocular abnormalities, short stature, and infections are common manifestations. There are both photosensitive and non-photosensitive forms of the disorder. TTD6 patients do not manifest cutaneous photosensitivity. Inheritance pattern has been reported to be autosomal recessive. The disease is caused by variants affecting the gene represented in this entry.

Interactions

29 interactions

InteractorPartnerSourcesPublicationsLink
T2EB_HUMANT2EA_HUMANBioGRID, HPRD, IntAct, MINT11113176 12665589 16547462 17643375 22939629 25492609 26344197 28514442 32296183 7926747 9677423 details
T2EB_HUMANCDK7_HUMANBioGRID, IntAct23064645 29568061 details
T2EB_HUMANEXOC8_HUMANBioGRID, IntAct32296183 details
T2EB_HUMANTF2B_HUMANBioGRID, HPRD11113176 12665589 details
T2EB_HUMANJUN_HUMANBioGRID8628277 details
T2EB_HUMANKAT5_HUMANBioGRID, IntAct32296183 details
T2EB_HUMANHSC20_HUMANDIP24606901 details
T2EB_HUMANT2FA_HUMANBioGRID, HPRD11113176 9677423 details
T2EB_HUMANCRCM_HUMANBioGRID, IntAct21988832 details
T2EB_HUMANTBP_HUMANBioGRID, HPRD11113176 9677423 details
T2EB_HUMANPICK1_HUMANBioGRID, IntAct32296183 details
T2EB_HUMANXPA_HUMANBioGRID, HPRD7876263 details
T2EB_HUMANT2FB_HUMANBioGRID, HPRD11113176 9677423 details
T2EB_HUMANTF2AA_HUMANBioGRID, HPRD11509574 9618479 details
T2EB_HUMANSND1_HUMANBioGRID, HPRD7651391 details
T2EB_HUMANERCC3_HUMANBioGRID, HPRD7926747 8152490 details
T2EB_HUMANKLF5_HUMANBioGRID, HPRD9089417 details
T2EB_HUMANSP16H_HUMANHPRD10792464 details
T2EB_HUMANFOS_HUMANBioGRID8628277 details
T2EB_HUMANA4_HUMANBioGRID21244100 21832049 details
T2EB_HUMANT2EB_HUMANBioGRID9677423 details
T2EB_HUMANMDM2_HUMANBioGRID, HPRD9271120 details
T2EB_HUMANRPB1_HUMANBioGRID12665589 26344197 details
T2EB_HUMANMCAF1_HUMANBioGRID, HPRD10777215 19106100 details
T2EB_HUMANTF2H1_HUMANHPRD12665589 details
T2EB_HUMANCCNH_HUMANHPRD11113176 details
T2EB_HUMANMAT1_HUMANHPRD11113176 details
T2EB_HUMANERCC6_HUMANHPRD8999876 details
T2EB_HUMANNUP62_HUMANHPRD11113176 details