USF2
Sign in to saveAlso known as FIP, bHLHb12, upstream transcription factor 2, c-fos interacting
Gen der Spezies Homo sapiens
Gene data
USF2- Name
- upstream transcription factor 2, c-fos interacting
- Type
- protein-coding
- Position
- 35,268,485–35,279,821 (+)
- Aliases
- FIP, bHLHb12
- Ensembl
- ENSG00000105698
- RefSeq RNA
- NM_001321150.2, NM_003367.4, NM_207291.3, XM_005259197.5, XM_011527260.3
- RefSeq protein
- NP_001308079.1, NP_003358.1, NP_997174.1, XP_005259254.1, XP_011525562.1
This gene encodes a member of the basic helix-loop-helix leucine zipper family of transcription factors. The encoded protein can activate transcription through pyrimidine-rich initiator (Inr) elements and E-box motifs and is involved in regulating multiple cellular processes. [provided by RefSeq, Mar 2016].
Gene Ontology
Biological process
regulation of transcription by RNA polymerase IIglucose mediated signaling pathwayglucose mediated signaling pathwayglucose mediated signaling pathwayglucose mediated signaling pathwaylate viral transcriptionpositive regulation of transcription by RNA polymerase IIpositive regulation of transcription by RNA polymerase II
Molecular function
RNA polymerase II cis-regulatory region sequence-specific DNA bindingDNA-binding transcription factor activity, RNA polymerase II-specificDNA-binding transcription factor activity, RNA polymerase II-specificDNA-binding transcription factor activity, RNA polymerase II-specificDNA-binding transcription activator activity, RNA polymerase II-specificDNA-binding transcription activator activity, RNA polymerase II-specificDNA-binding transcription activator activity, RNA polymerase II-specificDNA binding
Cellular component
Pathways
via MyGene.info
Gene · Ensembl
upstream transcription factor 2, c-fos interacting
- Symbol
- USF2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 19:35,268,485-35,279,821
- Strand
- Forward (+)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 2527
- exact match
- identifiers.org/ncbigene/7392
- found in taxon
- Homo sapiens
- genomic start
- 35268962
- chromosome
- human chromosome 19
- genomic end
- 35770724
- cytogenetic location
- 19q13.12
Sources (3)
via Wikidata · CC0