Identity
HGNC
LOCATION
14q32.33
LOCUSID
ALIAS
C14orf151,C14orf173,CMTDIE,FSGS5,pp9484
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 64423
MIM: 610982
HGNC: 23791
Ensembl: ENSG00000203485
Variants:
dbSNP: 64423
ClinVar: 64423
TCGA: ENSG00000203485
COSMIC: INF2
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38233384 | 2024 | Phosphorylation of INF2 by AMPK promotes mitochondrial fission and oncogenic function in endometrial cancer. | 1 |
| 38270181 | 2024 | Functional genetic variants of the disulfidptosis-related INF2 gene predict survival of hepatitis B virus-related hepatocellular carcinoma. | 0 |
| 38916773 | 2024 | INF2 formin variants linked to human inherited kidney disease reprogram the transcriptome, causing mitotic chaos and cell death. | 0 |
| 38233384 | 2024 | Phosphorylation of INF2 by AMPK promotes mitochondrial fission and oncogenic function in endometrial cancer. | 1 |
| 38270181 | 2024 | Functional genetic variants of the disulfidptosis-related INF2 gene predict survival of hepatitis B virus-related hepatocellular carcinoma. | 0 |
| 38916773 | 2024 | INF2 formin variants linked to human inherited kidney disease reprogram the transcriptome, causing mitotic chaos and cell death. | 0 |
| 36637069 | 2023 | INF2 mutations in patients with a broad phenotypic spectrum of Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis. | 0 |
| 37344480 | 2023 | FBXO7, a tumor suppressor in endometrial carcinoma, suppresses INF2-associated mitochondrial division. | 3 |
| 36637069 | 2023 | INF2 mutations in patients with a broad phenotypic spectrum of Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis. | 0 |
| 37344480 | 2023 | FBXO7, a tumor suppressor in endometrial carcinoma, suppresses INF2-associated mitochondrial division. | 3 |
| 34698992 | 2022 | Role of formin INF2 in human diseases. | 8 |
| 34698992 | 2022 | Role of formin INF2 in human diseases. | 8 |
| 31871199 | 2020 | Regulation of INF2-mediated actin polymerization through site-specific lysine acetylation of actin itself. | 24 |
| 31924668 | 2020 | FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes. | 12 |
| 32727404 | 2020 | Multiple formin proteins participate in glioblastoma migration. | 13 |
Citation
Dessen P
INF2 (inverted formin 2)
Atlas Genet Cytogenet Oncol Haematol. 2017-08-01
Online version: http://atlasgeneticsoncology.org/gene/57037/inf2-(inverted-formin-2)
