INS-IGF2 (INS-IGF2 readthrough)

2019-04-01  

Identity

HGNC
LOCATION
11p15.5
LOCUSID
ALIAS
INSIGF
FUSION GENES

Other Information

Locus ID:

NCBI: 723961
HGNC: 33527
Ensembl: ENSG00000284779

Variants:

dbSNP: 723961
ClinVar: 723961
TCGA: ENSG00000284779
COSMIC: INS-IGF2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000284779ENST00000643349A0A2R8Y747

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA164713176Platinum compoundsChemicalVariantAnnotationassociatedPD30672383
PA445204Ovarian NeoplasmsDiseaseVariantAnnotationassociatedPD30672383

References

Pubmed IDYearTitleCitations
199131212009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.85
251021802014Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.77
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.11
239350952013Autoimmunity against INS-IGF2 protein expressed in human pancreatic islets.0
251022592012Periconception maternal smoking and low education are associated with methylation of INSIGF in children at the age of 17 months.0
308033592019lncINS-IGF2 Promotes Cell Proliferation and Migration by Promoting G1/S Transition in Lung Cancer.0

Citation

Dessen P

INS-IGF2 (INS-IGF2 readthrough)

Atlas Genet Cytogenet Oncol Haematol. 2019-04-01

Online version: http://atlasgeneticsoncology.org/gene/57920/ins-igf2