ADGRB1


Summary: Angiogenesis is controlled by a local balance between stimulators and inhibitors of new vessel growth and is suppressed under normal physiologic conditions. Angiogenesis has been shown to be essential for growth and metastasis of solid tumors. In order to obtain blood supply for their growth, tumor cells are potently angiogenic and attract new vessels as results of increased secretion of inducers and decreased production of endogenous negative regulators. BAI1 contains at least one 'functional' p53-binding site within an intron, and its expression has been shown to be induced by wildtype p53. There are two other brain-specific angiogenesis inhibitor genes, designated BAI2 and BAI3 which along with BAI1 have similar tissue specificities and structures, however only BAI1 is transcriptionally regulated by p53. BAI1 is postulated to be a member of the secretin receptor family, an inhibitor of angiogenesis and a growth suppressor of glioblastomas [provided by RefSeq, Jul 2008].

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GO terms in ADGRB1


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Term Type
Evidence Type
GO Term ID
GO Des.
MF ISS GO:0001530 lipopolysaccharide binding
MF ISS GO:0001786 phosphatidylserine binding
MF IBA GO:0001965 G-protein alpha-subunit binding
MF IBA GO:0004930 G-protein coupled receptor activity
MF IDA GO:0004930 G-protein coupled receptor activity
MF IPI GO:0005515 protein binding
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Gene expression in normal tissue: ADGRB1

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in ADGRB1


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Database
Pathway ID
Pathway Des.
kegg hsa04115 p53 signaling pathway - Homo sapiens (human)
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD171 Pemetrexed 3
iGMDRD294 Batimastat 2
iGMDRD441 TW 37 4
iGMDRD138 PX 12 4
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in ADGRB1

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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