GCFC2

GC-rich sequence DNA-binding factor is a protein that in humans is encoded by the GCFC2 gene.[5][6][7][8]

GCFC2
Identifiers
AliasesGCFC2, C2orf3, DNABF, GCF, TCF9, GC-rich sequence DNA-binding factor 2
External IDsOMIM: 189901 MGI: 2141656 HomoloGene: 2411 GeneCards: GCFC2
Orthologs
SpeciesHumanMouse
Entrez

6936

330361

Ensembl

ENSG00000005436

ENSMUSG00000035125

UniProt

P16383

Q8BKT3

RefSeq (mRNA)

NM_001201334
NM_001201335
NM_003203

NM_177884

RefSeq (protein)

NP_001188263
NP_001188264
NP_003194

NP_808552

Location (UCSC)Chr 2: 75.65 – 75.71 MbChr 6: 81.92 – 81.96 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The first mRNA transcript isolated for this gene was part of an artificial chimera derived from two distinct gene transcripts and a primer used in the cloning process (see Genbank accession M29204). A positively charged amino terminus present only in the chimera was determined to bind GC-rich DNA, thus mistakenly thought to identify a transcription factor gene.[8]

References

  1. GRCh38: Ensembl release 89: ENSG00000005436 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000035125 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Johnson AC, Kageyama R, Popescu NC, Pastan I (Feb 1992). "Expression and chromosomal localization of the gene for the human transcriptional repressor GCF". J Biol Chem. 267 (3): 1689–94. doi:10.1016/S0021-9258(18)46000-0. PMID 1370479.
  6. Kageyama R, Pastan I (Jan 1990). "Molecular cloning and characterization of a human DNA binding factor that represses transcription". Cell. 59 (5): 815–25. doi:10.1016/0092-8674(89)90605-3. PMID 2556218. S2CID 21177070.
  7. Anthoni H, Zucchelli M, Matsson H, Muller-Myhsok B, Fransson I, Schumacher J, Massinen S, Onkamo P, Warnke A, Griesemann H, Hoffmann P, Nopola-Hemmi J, Lyytinen H, Schulte-Korne G, Kere J, Nothen MM, Peyrard-Janvid M (Apr 2007). "A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia". Hum Mol Genet. 16 (6): 667–77. doi:10.1093/hmg/ddm009. PMID 17309879.
  8. "Entrez Gene: C2orf3 chromosome 2 open reading frame 3".

Further reading


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