SFMBT1 (Scm like with four mbt domains 1)

2004-11-01  

Identity

HGNC
LOCATION
3p21.1
LOCUSID
ALIAS
RU1,SFMBT,hSFMBT
FUSION GENES

Other Information

Locus ID:

NCBI: 51460
MIM: 607319
HGNC: 20255
Ensembl: ENSG00000163935

Variants:

dbSNP: 51460
ClinVar: 51460
TCGA: ENSG00000163935
COSMIC: SFMBT1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000163935ENST00000394752Q9UHJ3
ENSG00000163935ENST00000394752A0A024R338
ENSG00000163935ENST00000482396C9IY64
ENSG00000163935ENST00000483069C9IZZ5
ENSG00000163935ENST00000497586C9JWI3

Expression (GTEx)

0
10
20
30
40
50
60

References

Pubmed IDYearTitleCitations
349781672022Regulatory Variant rs2535629 in ITIH3 Intron Confers Schizophrenia Risk By Regulating CTCF Binding and SFMBT1 Expression.7
349781672022Regulatory Variant rs2535629 in ITIH3 Intron Confers Schizophrenia Risk By Regulating CTCF Binding and SFMBT1 Expression.7
334810172021Multi-omics analysis to identify susceptibility genes for colorectal cancer.9
334810172021Multi-omics analysis to identify susceptibility genes for colorectal cancer.9
320234832020Genome-wide Screening Identifies SFMBT1 as an Oncogenic Driver in Cancer with VHL Loss.36
320234832020Genome-wide Screening Identifies SFMBT1 as an Oncogenic Driver in Cancer with VHL Loss.36
298860712018MiR-20a-3p regulates TGF-β1/Survivin pathway to affect keratinocytes proliferation and apoptosis by targeting SFMBT1 in vitro.13
298860712018MiR-20a-3p regulates TGF-β1/Survivin pathway to affect keratinocytes proliferation and apoptosis by targeting SFMBT1 in vitro.13
287896182017Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population.4
287896182017Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population.4
278615352016A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study.13
278615352016A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study.13
233494612013Proteomic and functional analyses reveal the role of chromatin reader SFMBT1 in regulating epigenetic silencing and the myogenic gene program.21
235927952013SFMBT1 functions with LSD1 to regulate expression of canonical histone genes and chromatin-related factors.48
239283052013The malignant brain tumor (MBT) domain protein SFMBT1 is an integral histone reader subunit of the LSD1 demethylase complex for chromatin association and epithelial-to-mesenchymal transition.27

Citation

Dessen P

SFMBT1 (Scm like with four mbt domains 1)

Atlas Genet Cytogenet Oncol Haematol. 2004-11-01

Online version: http://atlasgeneticsoncology.org/gene/42951/sfmbt1-(scm-like-with-four-mbt-domains-1)