TNFSF12-TNFSF13 (TNFSF12-TNFSF13 readthrough)

2004-06-01  

Identity

HGNC
TNFSF12-TNFSF13
LOCATION
17p13.1
LOCUSID
407977
ALIAS
TWE-PRIL
FUSION GENES
Show Gene Fusions

Other Information

Locus ID:

NCBI: 407977
HGNC: 33537
Ensembl: ENSG00000248871

Variants:

dbSNP: 407977
ClinVar: 407977
TCGA: ENSG00000248871
COSMIC: TNFSF12-TNFSF13

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000248871ENST00000293826A0A0A6YY99

Protein levels (Protein atlas)

Not detected
Low
Medium
High
N/A

References

Pubmed IDYearTitleCitations
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.15
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.15
199131212009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.105
199131212009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.105

Citation

Dessen P

TNFSF12-TNFSF13 (TNFSF12-TNFSF13 readthrough)

Atlas Genet Cytogenet Oncol Haematol. 2004-06-01

Online version: http://atlasgeneticsoncology.org/gene/42908/favicon/manifest.json