Entity Details

Primary name ARNT2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9HBZ2
EntryNameARNT2_HUMAN
FullNameAryl hydrocarbon receptor nuclear translocator 2
TaxID9606
Evidenceevidence at protein level
Length717
SequenceStatuscomplete
DateCreated2001-10-18
DateModified2021-06-02

Ontological Relatives

GenesARNT2

GO terms

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GOName
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:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific
GO:0001666 response to hypoxia
GO:0001701 in utero embryonic development
GO:0003700 DNA-binding transcription factor activity
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005667 transcription regulator complex
GO:0005737 cytoplasm
GO:0006355 regulation of transcription, DNA-templated
GO:0006357 regulation of transcription by RNA polymerase II
GO:0006805 xenobiotic metabolic process
GO:0007417 central nervous system development
GO:0007420 brain development
GO:0008284 positive regulation of cell population proliferation
GO:0017162 aryl hydrocarbon receptor binding
GO:0032355 response to estradiol
GO:0034751 aryl hydrocarbon receptor complex
GO:0043066 negative regulation of apoptotic process
GO:0044877 protein-containing complex binding
GO:0045893 positive regulation of transcription, DNA-templated
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0046982 protein heterodimerization activity
GO:1990837 sequence-specific double-stranded DNA binding

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR000014 PAS domainDomainDomain
IPR001067 Nuclear translocatorFamilyFamily
IPR001610 PAC motifRepeatRepeat
IPR011598 Myc-type, basic helix-loop-helix (bHLH) domainDomainDomain
IPR013655 PAS fold-3DomainDomain
IPR013767 PAS foldDomainDomain
IPR035965 PAS domain superfamilyFamilyHomologous superfamily
IPR036638 Helix-loop-helix DNA-binding domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
615926 OMIMWebb-Dattani syndrome (WEDAS)A disorder characterized by postnatal microcephaly with fronto-temporal lobe hypoplasia, multiple pituitary hormone deficiency, global developmental delay, seizures, severe visual impairment and abnormalities of the kidneys and urinary tract. The disease is caused by variants affecting the gene represented in this entry.

Interactions

72 interactions

InteractorPartnerSourcesPublicationsLink
ARNT2_HUMANUBP7_HUMANBioGRID, HPRD, IntAct16713569 details
ARNT2_HUMANSH3G2_HUMANBioGRID, IntAct21988832 details
ARNT2_HUMANTX1B3_HUMANBioGRID, IntAct21988832 details
ARNT2_HUMANDGCR6_HUMANBioGRID, IntAct24722188 details
ARNT2_HUMANTRAF4_HUMANBioGRID, IntAct24722188 28514442 details
ARNT2_HUMANHIF1A_HUMANBioGRID, HPRD, IntAct24722188 28514442 8927054 details
ARNT2_HUMANSIM2_HUMANBioGRID, IntAct14701734 27472814 28514442 details
ARNT2_HUMANEPAS1_HUMANBioGRID, IntAct20211142 23275444 details
ARNT2_HUMANNPAS4_HUMANBioGRID, HPRD14701734 24465693 details
ARNT2_HUMANA4_HUMANBioGRID21832049 details
ARNT2_HUMANRIMB1_HUMANBioGRID24722188 details
ARNT2_HUMANNPAS2_HUMANBioGRID24722188 details
ARNT2_HUMANCTBP1_HUMANBioGRID24722188 details
ARNT2_HUMANATL4_HUMANBioGRID24722188 details
ARNT2_HUMANCACO2_HUMANBioGRID24722188 details
ARNT2_HUMANCCD33_HUMANBioGRID24722188 details
ARNT2_HUMANCDR2_HUMANBioGRID24722188 details
ARNT2_HUMANCE57L_HUMANBioGRID24722188 details
ARNT2_HUMANCEP63_HUMANBioGRID24722188 details
ARNT2_HUMANDTX2_HUMANBioGRID24722188 32296183 details
ARNT2_HUMANDYDC1_HUMANBioGRID24722188 details
ARNT2_HUMANGOGA2_HUMANBioGRID24722188 details
ARNT2_HUMANIKZF3_HUMANBioGRID24722188 details
ARNT2_HUMANKIFC3_HUMANBioGRID24722188 details
ARNT2_HUMANLZTS2_HUMANBioGRID24722188 details
ARNT2_HUMANMAGA4_HUMANBioGRID24722188 details
ARNT2_HUMANMEIS2_HUMANBioGRID24722188 details
ARNT2_HUMANMEOX2_HUMANBioGRID24722188 details
ARNT2_HUMANMIPO1_HUMANBioGRID24722188 details
ARNT2_HUMANMTUS2_HUMANBioGRID24722188 details
ARNT2_HUMANNCOA3_HUMANBioGRID24722188 details
ARNT2_HUMANMYOME_HUMANBioGRID24722188 details
ARNT2_HUMANPLS1_HUMANBioGRID24722188 details
ARNT2_HUMANHOIL1_HUMANBioGRID24722188 details
ARNT2_HUMANREL_HUMANBioGRID24722188 details
ARNT2_HUMANRFX6_HUMANBioGRID24722188 details
ARNT2_HUMANRIM3A_HUMANBioGRID24722188 details
ARNT2_HUMANRINT1_HUMANBioGRID24722188 details
ARNT2_HUMANVINEX_HUMANBioGRID24722188 details
ARNT2_HUMANSPAG5_HUMANBioGRID24722188 details
ARNT2_HUMANSSBP3_HUMANBioGRID24722188 details
ARNT2_HUMANADIP_HUMANBioGRID24722188 details
ARNT2_HUMANSYCE1_HUMANBioGRID24722188 details
ARNT2_HUMANTACC3_HUMANBioGRID24722188 details
ARNT2_HUMANTAD2A_HUMANBioGRID24722188 details
ARNT2_HUMANTFP11_HUMANBioGRID24722188 details
ARNT2_HUMANTRAF1_HUMANBioGRID24722188 details
ARNT2_HUMANTRAF2_HUMANBioGRID24722188 details
ARNT2_HUMANTRI23_HUMANBioGRID24722188 details
ARNT2_HUMANTRI27_HUMANBioGRID24722188 details
ARNT2_HUMANTRI37_HUMANBioGRID24722188 details
ARNT2_HUMANTRI42_HUMANBioGRID24722188 details
ARNT2_HUMANTRIP6_HUMANBioGRID24722188 details
ARNT2_HUMANUSBP1_HUMANBioGRID24722188 details
ARNT2_HUMANVPS52_HUMANBioGRID24722188 details
ARNT2_HUMANZN341_HUMANBioGRID24722188 details
ARNT2_HUMANNDE1_HUMANBioGRID24722188 details
ARNT2_HUMANNPAS3_HUMANBioGRID24722188 details
ARNT2_HUMANAHR_HUMANBioGRID18096572 details
ARNT2_HUMANMAGD1_HUMANBioGRID27472814 details
ARNT2_HUMANSIM1_HUMANBioGRID27472814 32296183 details
ARNT2_HUMANPSB1_HUMANBioGRID32296183 details
ARNT2_HUMANAP1M1_HUMANBioGRID32296183 details
ARNT2_HUMANSTK16_HUMANBioGRID32296183 details
ARNT2_HUMANCAN7_HUMANBioGRID32296183 details
ARNT2_HUMANRBTN2_HUMANBioGRID32296183 details
ARNT2_HUMANOSGI1_HUMANBioGRID32296183 details
ARNT2_HUMANLMO4_HUMANBioGRID32296183 details
ARNT2_HUMANFAP20_HUMANBioGRID32296183 details
ARNT2_HUMANAP3M1_HUMANBioGRID32296183 details
ARNT2_HUMANARNT2_HUMANHPRD8927054 details
ARNT2_HUMANARNT_HUMANHPRD8927054 details