AKAP9


Summary: The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. Alternate splicing of this gene results in at least two isoforms that localize to the centrosome and the Golgi apparatus, and interact with numerous signaling proteins from multiple signal transduction pathways. These signaling proteins include type II protein kinase A, serine/threonine kinase protein kinase N, protein phosphatase 1, protein phosphatase 2a, protein kinase C-epsilon and phosphodiesterase 4D3. [provided by RefSeq, Aug 2008].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:604001
PHARMGKB IDPA24673
Map Location7q21.2

GO terms in AKAP9


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Term Type
Evidence Type
GO Term ID
GO Des.
MF IEA GO:0003677 DNA binding
MF TAS GO:0005088 Ras guanyl-nucleotide exchange factor activity
MF TAS GO:0005102 signaling receptor binding
MF IPI GO:0005515 protein binding
MF IBA GO:0015459 potassium channel regulator activity
MF IMP GO:0015459 potassium channel regulator activity
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Gene expression in normal tissue: AKAP9

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in AKAP9


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Database
Pathway ID
Pathway Des.
wikipathways WP35 G Protein Signaling Pathways
wikipathways WP4008 NO-cGMP-PKG mediated Neuroprotection
biocarta akapcentrosomepathway protein kinase a at the centrosome
reactome R-HSA-112314 Neurotransmitter receptors and postsynaptic signal transmission
reactome R-HSA-112315 Transmission across Chemical Synapses
reactome R-HSA-112316 Neuronal System
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD79 Gemcitabine 1
iGMDRD84 Lovastatin acid 2
iGMDRD512 nutlin 3 2
iGMDRD123 Isoevodiamine 2
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in AKAP9

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
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