RFX3

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

RFX3

Transcription factor RFX3 is a protein that in humans is encoded by the RFX3 gene.[5][6]

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RFX3
Identifiers
AliasesRFX3, regulatory factor X3
External IDsOMIM: 601337; MGI: 106582; HomoloGene: 7917; GeneCards: RFX3; OMA:RFX3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001282116
NM_001282117
NM_002919
NM_134428
NM_001377999

NM_001166414
NM_011265
NM_001360357
NM_001360358

RefSeq (protein)

NP_001269045
NP_001269046
NP_002910
NP_602304
NP_001364928

NP_001159886
NP_035395
NP_001347286
NP_001347287

Location (UCSC)Chr 9: 3.22 – 3.53 MbChr 19: 27.74 – 27.99 Mb
PubMed search[3][4]
Wikidata
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This gene is a member of the regulatory factor X gene family, which encodes transcription factors that contain a highly-conserved winged helix DNA binding domain. The protein encoded by this gene is structurally related to regulatory factors X1, X2, X4, and X5. It is a transcriptional activator that can bind DNA as a monomer or as a heterodimer with other RFX family members. Two transcript variants encoding different isoforms have been described for this gene, and at least one of the variants utilizes alternative polyadenylation signals.[6]

References

Further reading

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