INF2 (inverted formin 2)

2017-08-01  

Identity

HGNC
LOCATION
14q32.33
LOCUSID
ALIAS
C14orf151,C14orf173,CMTDIE,FSGS5,pp9484
FUSION GENES

Other Information

Locus ID:

NCBI: 64423
MIM: 610982
HGNC: 23791
Ensembl: ENSG00000203485

Variants:

dbSNP: 64423
ClinVar: 64423
TCGA: ENSG00000203485
COSMIC: INF2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000203485ENST00000252527A0A0A0MQU1
ENSG00000203485ENST00000330634Q27J81
ENSG00000203485ENST00000392634Q27J81
ENSG00000203485ENST00000398337Q27J81
ENSG00000203485ENST00000617571Q8WYS3

Expression (GTEx)

0
50
100
150
200
250

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
382333842024Phosphorylation of INF2 by AMPK promotes mitochondrial fission and oncogenic function in endometrial cancer.1
382701812024Functional genetic variants of the disulfidptosis-related INF2 gene predict survival of hepatitis B virus-related hepatocellular carcinoma.0
389167732024INF2 formin variants linked to human inherited kidney disease reprogram the transcriptome, causing mitotic chaos and cell death.0
382333842024Phosphorylation of INF2 by AMPK promotes mitochondrial fission and oncogenic function in endometrial cancer.1
382701812024Functional genetic variants of the disulfidptosis-related INF2 gene predict survival of hepatitis B virus-related hepatocellular carcinoma.0
389167732024INF2 formin variants linked to human inherited kidney disease reprogram the transcriptome, causing mitotic chaos and cell death.0
366370692023INF2 mutations in patients with a broad phenotypic spectrum of Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.0
373444802023FBXO7, a tumor suppressor in endometrial carcinoma, suppresses INF2-associated mitochondrial division.3
366370692023INF2 mutations in patients with a broad phenotypic spectrum of Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.0
373444802023FBXO7, a tumor suppressor in endometrial carcinoma, suppresses INF2-associated mitochondrial division.3
346989922022Role of formin INF2 in human diseases.8
346989922022Role of formin INF2 in human diseases.8
318711992020Regulation of INF2-mediated actin polymerization through site-specific lysine acetylation of actin itself.24
319246682020FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes.12
327274042020Multiple 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)