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Dysbindin information


DTNBP1
Identifiers
AliasesDTNBP1, BLOC1S8, DBND, HPS7, My031, SDY, dystrobrevin binding protein 1
External IDsOMIM: 607145; MGI: 2137586; HomoloGene: 12037; GeneCards: DTNBP1; OMA:DTNBP1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001271667
NM_001271668
NM_001271669
NM_032122
NM_183040

NM_025772

RefSeq (protein)

NP_001258596
NP_001258597
NP_001258598
NP_115498
NP_898861

NP_080048

Location (UCSC)Chr 6: 15.52 – 15.66 MbChr 13: 45.08 – 45.16 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Dysbindin, short for dystrobrevin-binding protein 1, is a protein constituent of the dystrophin-associated protein complex (DPC) of skeletal muscle cells. It is also a part of BLOC-1, or biogenesis of lysosome-related organelles complex 1. Dysbindin was discovered by the research group of Derek Blake via yeast two-hybrid screening for binding partners of α-dystrobrevin.[5] In addition, dysbindin is found in neural tissue of the brain, particularly in axon bundles and especially in certain axon terminals, notably mossy fiber synaptic terminals in the cerebellum and hippocampus.[5] In humans, dysbindin is encoded by the DTNBP1 gene.[5]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000047579 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000057531 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b c Benson; Newey, SE; Martin-Rendon, E; Hawkes, R; Blake, DJ; et al. (2001). "Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain". J Biol Chem. 276 (26): 24232–41. doi:10.1074/jbc.M010418200. PMID 11316798.

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Dysbindin

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Dysbindin, short for dystrobrevin-binding protein 1, is a protein constituent of the dystrophin-associated protein complex (DPC) of skeletal muscle cells...

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Substantia nigra

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reduced dysbindin expression. Increased NMDA receptors may point to the involvement of glutamate-dopamine interactions in schizophrenia. Dysbindin, which...

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Animal model of schizophrenia

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antipsychotic clozapine. Dysbindin is a protein coded for by the gene DTNBP1, which has been linked to schizophrenia. Dysbindin may be involved in the changes...

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Clanging

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FOXP2 (which is linked to a familial language disorder and autism) and dysbindin 1 genes43,44. This distal explanation not only does not explain clanging...

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Psychotic depression

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Hohoff, Christa; Birosova, Eva; Arolt, Volker; Baune, Bernhard T. (2011). "Dysbindin (DTNBP1) – A role in psychotic depression?". Journal of Psychiatric Research...

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DBNDD2

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Dysbindin domain-containing protein 2 is a protein that in humans is encoded by the DBNDD2 gene. GRCh38: Ensembl release 89: ENSG00000244274 – Ensembl...

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Risk factors of schizophrenia

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reviews suggested that the evidence was strongest for two genes known as dysbindin (DTNBP1) and neuregulin (NRG1), and that a number of other genes (such...

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Childhood schizophrenia

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indicated in children diagnosed with schizophrenia that include: neuregulin, dysbindin, D-amino acid oxidase, proline dehydrogenase, catechol-Omethyltransferase...

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TRIM32

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HIV-1 genes. TRIM32 has been shown to interact with: actin, ABI2 c-Myc, dysbindin, and piasy, Currently, TRIM32 is believed to employ two different mechanisms...

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Chromosome 20

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CCCTC-binding factor-like CTNNBL1: Beta-catenin-like protein 1 DBNDD2: Dysbindin domain-containing protein 2 DDX27: DEAD box polypeptide 27 DEFB118, DEFB119...

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MUTED

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reading frame for this gene. MUTED has been shown to interact with BLOC1S2, Dysbindin and PLDN. GRCh38: Ensembl release 89: ENSG00000188428 – Ensembl, May 2017...

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Dystrobrevin beta

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Starcevic M, Spencer MJ, Dell'Angelica EC (2006). "Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1)...

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SNAPAP

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dock vesicles. SNAPAP has been shown to interact with: BLOC1S1, BLOC1S2, Dysbindin, PLDN, RGS7, SNAP-25, SNAP23, and TRPV1. GRCh38: Ensembl release 89: ENSG00000143553...

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Rs6313

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V. E. (2012). "Polymorphism of serotonin receptor genes (5-HTR2A) and dysbindin (DTNBP1) and individual components of short-term verbal memory processes...

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PLDN

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determined. PLDN has been shown to interact with: BLOC1S1, BLOC1S2, CNO, Dysbindin, MUTED, SNAPAP, and STX12. GRCh38: Ensembl release 89: ENSG00000104164...

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List of genes mutated in cutaneous conditions

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Brooke–Spiegler syndrome Cylindroma DHCR7 Smith–Lemli–Opitz syndrome DTNBP1 Dysbindin Hermansky–Pudlak syndrome type 7 Dyskerin Dyskeratosis congenita ECM1...

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Derek Blake

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Benson M.A., Newey S.E., Martin-Rendon E., Hawkes R. and Blake D.J. (2001) Dysbindin, a novel coiled-coil containing protein that interacts with the dystrobrevins...

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CSNK1D

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magnitude. On the contrary, proteins being homologous to CK1BP (e.g. dysbindin or BLOC-1 [biogenesis of lysosome-related organelles complex-1]) are able...

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BLOC1S2

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(2003). "Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)"...

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Dystrobrevin

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additional to α-dystrobrevin-binding proteins: β-synemin, syncoilin, and dysbindin. Syncoilin and β-synemin are both intermediate filament proteins. The...

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