Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7391
Gene name Gene Name - the full gene name approved by the HGNC.
Upstream transcription factor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
USF1
Synonyms (NCBI Gene) Gene synonyms aliases
FCHL, FCHL1, HYPLIP1, MLTF, MLTFI, UEF, bHLHb11
Disease Acronyms (UniProt) Disease acronyms from UniProt database
FCHL1
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q23.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the basic helix-loop-helix leucine zipper family, and can function as a cellular transcription factor. The encoded protein can activate transcription through pyrimidine-rich initiator (Inr) elements and E-box motifs. This gen
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs2073658 C>T Risk-factor Intron variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT045419 hsa-miR-149-5p CLASH 23622248
MIRT040599 hsa-miR-92b-3p CLASH 23622248
MIRT038834 hsa-miR-93-3p CLASH 23622248
MIRT1477105 hsa-miR-1285 CLIP-seq
MIRT1477106 hsa-miR-3187-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000430 Process Regulation of transcription from RNA polymerase II promoter by glucose IC 8576131
GO:0000432 Process Positive regulation of transcription from RNA polymerase II promoter by glucose IMP 7852331
GO:0000432 Process Positive regulation of transcription from RNA polymerase II promoter by glucose ISS
GO:0000785 Component Chromatin IDA 27141965
GO:0000785 Component Chromatin ISA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
191523 12593 ENSG00000158773
Protein
UniProt ID P22415
Protein name Upstream stimulatory factor 1 (Class B basic helix-loop-helix protein 11) (bHLHb11) (Major late transcription factor 1)
Protein function Transcription factor that binds to a symmetrical DNA sequence (E-boxes) (5'-CACGTG-3') that is found in a variety of viral and cellular promoters.
PDB 1AN4
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00010 HLH 200 255 Helix-loop-helix DNA-binding domain Domain
Sequence
MKGQQKTAETEEGTVQIQEGAVATGEDPTSVAIASIQSAATFPDPNVKYVFRTENGGQVM
YRVIQVSEGQLDGQTEGTGAISGYPATQSMTQAVIQGAFTSDDAVDTEGTAAETHYTYFP
STAVGDGAGGTTSGSTAAVVTTQGSEALLGQATPPGTGQFFVMMSPQEVLQGGSQRSIAP
RTHPYSPKSEAPRTTRDEKRRAQHNEVERRRRDKINNWIVQLSKIIPDCSMESTKSGQSK
GGILSKACDYIQELR
QSNHRLSEELQGLDQLQLDNDVLRQQVEDLKNKNLLLRAQLRHHG
LEVVIKNDSN
Sequence length 310
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Estrogen-dependent gene expression
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hyperlipidemia Hyperlipidemia, Familial Combined rs118204057, rs118204060, rs118204062, rs1563569634, rs118204069, rs118204070, rs118204071, rs1566946168, rs1064797075
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 22390463
Atherosclerosis Associate 18276913, 19910639, 24722012, 26068452
Azoospermia Associate 25374392
Brain Diseases Associate 22390463
Breast Neoplasms Associate 35414770
Carcinoma Hepatocellular Associate 25149140, 25480412
Carcinoma Renal Cell Associate 39993614
Cardiovascular Diseases Associate 16699592, 18974842, 24722012
Complement Component C1s Deficiency Associate 31537905
Congenital myasthenic syndrome ib Associate 12393509