Gene Gene information from NCBI Gene database.
Entrez ID 116986
Gene name ArfGAP with GTPase domain, ankyrin repeat and PH domain 2
Gene symbol AGAP2
Synonyms (NCBI Gene)
CENTG1GGAP2PIKE
Chromosome 12
Chromosome location 12q14.1
Summary The protein encoded by this gene belongs to the centaurin gamma-like family. It mediates anti-apoptotic effects of nerve growth factor by activating nuclear phosphoinositide 3-kinase. It is overexpressed in cancer cells, and promotes cancer cell invasion.
miRNA miRNA information provided by mirtarbase database.
96
miRTarBase ID miRNA Experiments Reference
MIRT771611 hsa-miR-1183 CLIP-seq
MIRT771612 hsa-miR-1324 CLIP-seq
MIRT771613 hsa-miR-1471 CLIP-seq
MIRT771614 hsa-miR-3156-3p CLIP-seq
MIRT771615 hsa-miR-3162-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
41
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0003924 Function GTPase activity IBA
GO:0003924 Function GTPase activity IDA 11136977, 12640130
GO:0003924 Function GTPase activity IEA
GO:0003924 Function GTPase activity TAS 18374643
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605476 16921 ENSG00000135439
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q99490
Protein name Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2 (AGAP-2) (Centaurin-gamma-1) (Cnt-g1) (GTP-binding and GTPase-activating protein 2) (GGAP2) (Phosphatidylinositol 3-kinase enhancer) (PIKE)
Protein function GTPase-activating protein (GAP) for ARF1 and ARF5, which also shows strong GTPase activity. Isoform 1 participates in the prevention of neuronal apoptosis by enhancing PI3 kinase activity. It aids the coupling of metabotropic glutamate receptor
PDB 2BMJ , 2IWR , 2RLO
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 408 568 Ras family Domain
PF01412 ArfGap 931 1046 Putative GTPase activating protein for Arf Domain
PF00023 Ank 1091 1122 Ankyrin repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Isoform 1 is brain-specific. Isoform 2 is ubiquitously expressed, with highest levels in brain and heart. {ECO:0000269|PubMed:12640130, ECO:0000269|PubMed:14761976, ECO:0000269|PubMed:15118108, ECO:0000269|PubMed:16079295, ECO:0000269|
Sequence
MSRGAGALQRRTTTYLISLTLVKLESVPPPPPSPSAAAVGAPGARGSEPRDPGSPRGAEE
PGKKRHERLFHRQDALWISTSSAGAGGAEPPALSPAPASPARPVSPAPGRRLSLWAAPPG
PPLSGGLSPDSKPGGAPSSSRRPLLSSPSWGGPEPEGRTGGGVPGSSSPHPGTGSRRLKV
APPPPAPKPCKTVTTSGAKAGGGKGAGSRLSWPESEGKPRVKGSKSSAGTGASVSAAATA
AAAGGGGSTASTSGGVGAGAGARGKLSPRKGKSKTLDNSDLHPGPPAGSPPPLTLPPTPS
PATAVTAASAQPPGPAPPITLEPPAPGLKRGREGGRASTRDRKMLKFISGIFTKSTGGPP
GSGPLPGPPSLSSGSGSRELLGAELRASPKAVINSQEWTLSRSIPELRLGVLGDARSGKS
SLIHRFLTGSYQVLEKTESEQYKKEMLVDGQTHLVLIREEAGAPDAKFSGWADAVIFVFS
LEDENSFQAVSRLHGQLSSLRGEGRGGLALALVGTQDRISASSPRVVGDARARALCADMK
RCSYYETCATYGLNVDRVFQEVAQKVVT
LRKQQQLLAACKSLPSSPSHSAASTPVAGQAS
NGGHTSDYSSSLPSSPNVGHRELRAEAAAVAGLSTPGSLHRAAKRRTSLFANRRGSDSEK
RSLDSRGETTGSGRAIPIKQSFLLKRSGNSLNKEWKKKYVTLSSNGFLLYHPSINDYIHS
THGKEMDLLRTTVKVPGKRPPRAISAFGPSASINGLVKDMSTVQMGEGLEATTPMPSPSP
SPSSLQPPPDQTSKHLLKPDRNLARALSTDCTPSGDLSPLSREPPPSPMVKKQRRKKLTT
PSKTEGSAGQAEAKRKMWKLKSFGSLRNIYKAEENFEFLIVSSTGQTWHFEAASFEERDA
WVQAIESQILASLQCCESSKVKLRTDSQSEAVAIQAIRNAKGNSICVDCGAPNPTWASLN
LGALICIECSGIHRNLGTHLSRVRSLDLDDWPRELTLVLTAIGNDTANRVWESDTRGRAK
PSRDSSREERESWIRAKYEQLLFLAP
LSTSEEPLGRQLWAAVQAQDVATVLLLLAHARHG
PLDTSVEDPQLRSPLHLAAELAHVVITQLLLWYGADVAARDAQGRTALFYARQAGSQLCA
DILLQHGCPGEGGSAATTPSAATTPSITATPSPRRRSSAASVGRADAPVALV
Sequence length 1192
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  FoxO signaling pathway
Endocytosis
 
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
15
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
AGAP2-related disorder Uncertain significance; Likely benign; Benign rs368433604, rs2540841782, rs148450672, rs41292015, rs148957106, rs17852479, rs542194963, rs551915207, rs35567553, rs201928942, rs2301553, rs149262637, rs932350430, rs115767833 RCV003404576
RCV003421116
RCV003923908
RCV003904100
RCV003977212
RCV003977365
RCV003939739
RCV003959360
RCV003924351
RCV003961925
RCV003926869
RCV003976762
RCV003976963
RCV003958115
Cervical cancer Uncertain significance rs771238162 RCV005937479
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 31989994
Breast Neoplasms Associate 22302350, 30157918, 30910994, 35369814
Carcinogenesis Associate 35707044
Carcinoma Non Small Cell Lung Stimulate 27195672
Carcinoma Non Small Cell Lung Associate 28209205, 28617550, 32015683
Carcinoma Renal Cell Associate 38036719
Carcinoma Squamous Cell Associate 26464646
Cholangiocarcinoma Associate 34034689
Colorectal Neoplasms Associate 32202509
Disease Resistance Associate 35707044