Entity Details

Primary name DLG3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ92796
EntryNameDLG3_HUMAN
FullNameDisks large homolog 3
TaxID9606
Evidenceevidence at protein level
Length817
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesDLG3

GO terms

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GOName
GO:0000165 MAPK cascade
GO:0005615 extracellular space
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0008285 negative regulation of cell population proliferation
GO:0010923 negative regulation of phosphatase activity
GO:0016323 basolateral plasma membrane
GO:0019900 kinase binding
GO:0019902 phosphatase binding
GO:0030054 cell junction
GO:0043113 receptor clustering
GO:0045197 establishment or maintenance of epithelial cell apical/basal polarity
GO:0061098 positive regulation of protein tyrosine kinase activity
GO:0097120 receptor localization to synapse
GO:0098609 cell-cell adhesion
GO:2000310 regulation of NMDA receptor activity

Subcellular Location

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Domains

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DomainNameCategoryType
IPR001452 SH3 domainDomainDomain
IPR001478 PDZ domainDomainDomain
IPR008144 Guanylate kinase-like domainDomainDomain
IPR008145 Guanylate kinase/L-type calcium channel beta subunitDomainDomain
IPR016313 Disks large 1-likeFamilyFamily
IPR019583 PDZ-associated domain of NMDA receptorsDomainDomain
IPR019590 Disks large homologue 1, N-terminal PEST domainDomainDomain
IPR020590 Guanylate kinase, conserved siteSiteConserved site
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily
IPR035763 Disks Large homologue 3, SH3 domainDomainDomain
IPR036028 SH3-like domain superfamilyFamilyHomologous superfamily
IPR036034 PDZ superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
300850 OMIMMental retardation, X-linked 90 (MRX90)A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations. The disease is caused by variants affecting the gene represented in this entry.

Interactions

59 interactions

InteractorPartnerSourcesPublicationsLink
DLG3_HUMANERBB4_HUMANBioGRID, HPRD, MINT10725395 12175853 details
DLG3_HUMANGUAD_HUMANBioGRID, HPRD, MINT10542258 10595517 details
DLG3_HUMANABCA1_HUMANHPRD, IntAct16192269 16192271 details
DLG3_HUMANPP1A_HUMANUniProt19389623 details
DLG3_HUMANOSBP2_HUMANBioGRID, IntAct32296183 details
DLG3_HUMANDHR11_HUMANBioGRID, IntAct32296183 details
DLG3_HUMANRS8_HUMANBioGRID, IntAct32296183 details
DLG3_HUMANERD21_HUMANBioGRID, IntAct32296183 details
DLG3_HUMANIF4H_HUMANBioGRID, IntAct32296183 details
DLG3_HUMANPKHA2_HUMANBioGRID, IntAct32296183 details
DLG3_HUMANDLGP2_HUMANIntAct32296183 details
DLG3_HUMANVTNC_HUMANBioGRID, IntAct32296183 details
DLG3_HUMANFRPD4_HUMANIntAct30126976 details
DLG3_HUMANARHG8_HUMANIntAct30126976 details
DLG3_HUMANF163B_HUMANIntAct30126976 details
DLG3_HUMANNMDE3_HUMANBioGRID, HPRD, IntAct11937501 30126976 details
DLG3_HUMANCLTR2_HUMANIntAct30126976 details
DLG3_HUMANLRP2_HUMANBioGRID, HPRD12713445 details
DLG3_HUMANAPC_HUMANBioGRID9188857 details
DLG3_HUMANEXOC4_HUMANBioGRID, HPRD12738960 details
DLG3_HUMANNMDE2_HUMANBioGRID, HPRD11937501 11997254 12738960 8780649 9278515 details
DLG3_HUMANEXOC7_HUMANBioGRID12738960 details
DLG3_HUMANFAK2_HUMANBioGRID, HPRD12576483 details
DLG3_HUMANSYGP1_HUMANBioGRID, HPRD9581761 details
DLG3_HUMANDLG4_HUMANBioGRID, HPRD10026200 28973854 details
DLG3_HUMANDLGP1_HUMANBioGRID32296183 9115257 details
DLG3_HUMANNLGN2_HUMANBioGRID9278515 details
DLG3_HUMANNLGN1_HUMANBioGRID9278515 details
DLG3_HUMANNLGN3_HUMANBioGRID, HPRD9278515 details
DLG3_HUMANNMDE1_HUMANBioGRID, HPRD11937501 12070168 9278515 details
DLG3_HUMANSEM4C_HUMANBioGRID, HPRD11134026 details
DLG3_HUMANAT2B4_HUMANBioGRID, HPRD11274188 details
DLG3_HUMANCRIPT_HUMANBioGRID, HPRD11937501 12070168 details
DLG3_HUMANKHDR1_HUMANBioGRID22745667 details
DLG3_HUMANOGT1_HUMANBioGRID32994395 details
DLG3_HUMANAGRL1_HUMANHPRD10958799 details
DLG3_HUMANDLGP4_HUMANHPRD9115257 details
DLG3_HUMANCALM1_HUMANHPRD10026200 details
DLG3_HUMANCALM2_HUMANHPRD10026200 details
DLG3_HUMANCALM3_HUMANHPRD10026200 details
DLG3_HUMANDLGP3_HUMANHPRD9115257 details
DLG3_HUMANDLG1_HUMANBioGRID, HPRD, IntAct12351654 26496610 details
DLG3_HUMANKCJ12_HUMANBioGRID, HPRD15024025 details
DLG3_HUMANEXOC3_HUMANBioGRID12738960 details
DLG3_HUMANGRIK2_HUMANBioGRID, HPRD12070168 9808460 details
DLG3_HUMANGRIK5_HUMANBioGRID9808460 details
DLG3_HUMANAT2B2_HUMANBioGRID11274188 details
DLG3_HUMANGCYA2_HUMANBioGRID, HPRD11572861 details
DLG3_HUMANLIN7A_HUMANHPRD9753324 details
DLG3_HUMANNMDZ1_HUMANHPRD10862698 details
DLG3_HUMANKCNA4_HUMANHPRD16637659 details
DLG3_HUMANMK12_HUMANHPRD16637659 details
DLG3_HUMANSCN4A_HUMANHPRD16637659 details
DLG3_HUMANCNKR2_HUMANHPRD16637659 details
DLG3_HUMANKIF1B_HUMANHPRD16637659 details
DLG3_HUMANCCG2_HUMANHPRD16637659 details
DLG3_HUMANSCN5A_HUMANHPRD16637659 details
DLG3_HUMANGLSL_HUMANHPRD16637659 details
DLG3_HUMANKCNJ2_HUMANHPRD16637659 details