Entity Details

Primary name DNMBP_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ6XZF7
EntryNameDNMBP_HUMAN
FullNameDynamin-binding protein
TaxID9606
Evidenceevidence at protein level
Length1577
SequenceStatuscomplete
DateCreated2004-12-07
DateModified2021-06-02

Ontological Relatives

GenesDNMBP

GO terms

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GOName
GO:0005085 guanyl-nucleotide exchange factor activity
GO:0005794 Golgi apparatus
GO:0005795 Golgi stack
GO:0005856 cytoskeleton
GO:0005911 cell-cell junction
GO:0007568 aging
GO:0008360 regulation of cell shape
GO:0035556 intracellular signal transduction
GO:0045202 synapse
GO:0098793 presynapse

Subcellular Location

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Subcellular Location
Cell junction
Cytoplasm
Golgi apparatus

Domains

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DomainNameCategoryType
IPR000219 Dbl homology (DH) domainDomainDomain
IPR001331 Guanine-nucleotide dissociation stimulator, CDC24, conserved siteSiteConserved site
IPR001452 SH3 domainDomainDomain
IPR004148 BAR domainDomainDomain
IPR027267 AH/BAR domain superfamilyFamilyHomologous superfamily
IPR035469 Dynamin-binding proteinFamilyFamily
IPR035817 Dynamin-binding protein, first N-terminal SH3 domainDomainDomain
IPR035818 Dynamin-binding protein, second N-terminal SH3 domainDomainDomain
IPR035819 Dynamin-binding protein, third N-terminal SH3 domainDomainDomain
IPR035820 Dynamin-binding protein, first C-terminal SH3 domainDomainDomain
IPR035899 Dbl homology (DH) domain superfamilyFamilyHomologous superfamily
IPR036028 SH3-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
618415 OMIMCataract 48 (CTRCT48)A form of cataract, 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. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. CTRCT48 is an autosomal recessive form characterized by infantile or early-childhood onset. The disease is caused by variants affecting the gene represented in this entry.

Interactions

30 interactions

InteractorPartnerSourcesPublicationsLink
DNMBP_HUMANTNFL6_HUMANBioGRID, IntAct19807924 details
DNMBP_HUMANBIN3_HUMANBioGRID, IntAct18654987 26186194 32203420 details
DNMBP_HUMANRHG17_HUMANBioGRID, IntAct18654987 details
DNMBP_HUMANBUB1B_HUMANBioGRID, IntAct18654987 details
DNMBP_HUMANWASL_HUMANBioGRID, DIP, HPRD14506234 24332715 details
DNMBP_HUMANDNMBP_HUMANDIP, HPRD14506234 24332715 details
DNMBP_HUMANEVL_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANDYN1_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANVASP_HUMANBioGRID14506234 34079125 details
DNMBP_HUMANENAH_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANKHDR1_HUMANBioGRID22745667 details
DNMBP_HUMANCNN1_HUMANBioGRID10220577 details
DNMBP_HUMANCDC42_HUMANBioGRID31478661 32203420 details
DNMBP_HUMANRAC1_HUMANBioGRID32203420 details
DNMBP_HUMANCYFP2_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANWASF1_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANHSP74_HUMANBioGRID14506234 details
DNMBP_HUMANWIPF2_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANDREB_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANACTS_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANTBA1A_HUMANBioGRID14506234 details
DNMBP_HUMANWIPF3_HUMANBioGRID14506234 details
DNMBP_HUMANNCKP1_HUMANBioGRID, HPRD14506234 details
DNMBP_HUMANMD2L2_HUMANBioGRID30022168 details
DNMBP_HUMANMEX3B_HUMANBioGRID29395067 details
DNMBP_HUMANTNR6B_HUMANBioGRID29395067 details
DNMBP_HUMANTULP3_HUMANBioGRID33187986 details
DNMBP_HUMANHS71A_HUMANHPRD14506234 details
DNMBP_HUMANHS71B_HUMANHPRD14506234 details
DNMBP_HUMANRAPH1_HUMANHPRD14506234 details