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p(HGNC:RAB7A)

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Entity

Name
RAB7A
Namespace
hgnc
Namespace Version
20180906
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/b46b65c3da259b6e86026514dfececab7c22a11b/external/hgnc-names.belns

Appears in Networks 3

Extracellular Tau and Its Potential Role in the Propagation of Tau Pathology v1.0.0

The Ubiquitin–Proteasome System and the Autophagic–Lysosomal System in Alzheimer Disease v1.0.0

Autophagy and the ubiquitin-proteasome system: collaborators in neuroprotection v1.0.0

In-Edges 3

p(HGNC:MAPT) association p(HGNC:RAB7A) View Subject | View Object

Rab7a (Rodriguez et al., 2017) and Rab1a (Mohamed et al., 2017) have been recently implicated in tau release, further suggesting that tau release involves vesicle transport. PubMed:29238289

Appears in Networks:
Annotations
MeSH
Blood
MeSH
Cerebrospinal Fluid

bp(GO:"regulation of endosome size") association p(HGNC:RAB7A) View Subject | View Object

Genes related to endocytosis, such as Rab5,Rab7, and Rab4, are among the earliest groups to showup-regulated transcription in AD(Ginsberg et al. 2010), and their corresponding proteins are abnormally recruited to endosomes, where they promote fusion and abnormal enlargement of early and late endosomes (Cataldo et al. 1997, 2008). PubMed:22908190

Appears in Networks:

path(MESH:"Alzheimer Disease") positiveCorrelation p(HGNC:RAB7A) View Subject | View Object

Genes related to endocytosis, such as Rab5,Rab7, and Rab4, are among the earliest groups to showup-regulated transcription in AD(Ginsberg et al. 2010), and their corresponding proteins are abnormally recruited to endosomes, where they promote fusion and abnormal enlargement of early and late endosomes (Cataldo et al. 1997, 2008). PubMed:22908190

Appears in Networks:

Out-Edges 7

p(HGNC:RAB7A) association p(HGNC:MAPT) View Subject | View Object

Rab7a (Rodriguez et al., 2017) and Rab1a (Mohamed et al., 2017) have been recently implicated in tau release, further suggesting that tau release involves vesicle transport. PubMed:29238289

Appears in Networks:
Annotations
MeSH
Blood
MeSH
Cerebrospinal Fluid

p(HGNC:RAB7A) increases a(GO:endosome) View Subject | View Object

Still other cargoes reach late endosomes when Rab7 and its effectors replace Rab5 and initiate further endosomal maturation (Poteryaev et al. 2010). PubMed:22908190

Appears in Networks:

p(HGNC:RAB7A) positiveCorrelation path(MESH:"Alzheimer Disease") View Subject | View Object

Genes related to endocytosis, such as Rab5,Rab7, and Rab4, are among the earliest groups to showup-regulated transcription in AD(Ginsberg et al. 2010), and their corresponding proteins are abnormally recruited to endosomes, where they promote fusion and abnormal enlargement of early and late endosomes (Cataldo et al. 1997, 2008). PubMed:22908190

Appears in Networks:

p(HGNC:RAB7A) increases complex(a(GO:"early endosome"), a(GO:"late endosome")) View Subject | View Object

Genes related to endocytosis, such as Rab5,Rab7, and Rab4, are among the earliest groups to showup-regulated transcription in AD(Ginsberg et al. 2010), and their corresponding proteins are abnormally recruited to endosomes, where they promote fusion and abnormal enlargement of early and late endosomes (Cataldo et al. 1997, 2008). PubMed:22908190

Appears in Networks:

p(HGNC:RAB7A) association bp(GO:"regulation of endosome size") View Subject | View Object

Genes related to endocytosis, such as Rab5,Rab7, and Rab4, are among the earliest groups to showup-regulated transcription in AD(Ginsberg et al. 2010), and their corresponding proteins are abnormally recruited to endosomes, where they promote fusion and abnormal enlargement of early and late endosomes (Cataldo et al. 1997, 2008). PubMed:22908190

Appears in Networks:

p(HGNC:RAB7A) hasVariant p(HGNC:RAB7A, var("?")) View Subject | View Object

Appears in Networks:

p(HGNC:RAB7A) increases bp(GO:"autophagosome-lysosome fusion") View Subject | View Object

Rab7 participates in trafficking autophagosomes and fusion with lysosomes and disease-causing mutations are predicted to impair this process [43–45]. PubMed:18930136

Appears in Networks:

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.