YTHDF2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | YTHDF2 , HGRG8, NY-REN-2, CAHL, YTH N6-methyladenosine RNA binding protein 2, DF2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 610640 MGI: 2444233 HomoloGene: 32302 GeneCards: YTHDF2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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YTH N6-methyladenosine RNA binding protein 2 is a protein that in humans is encoded by the YTHDF2 gene. [5]
This gene encodes a member of the YTH (YT521-B homology) superfamily containing YTH domain. The YTH domain is typical for the eukaryotes and is particularly abundant in plants. The YTH domain is usually located in the middle of the protein sequence and may function in binding to RNA. In addition to a YTH domain, this protein has a proline-rich region which may be involved in signal transduction. An Alu-rich domain has been identified in one of the introns of this gene, which is thought to be associated with human longevity. Also, reciprocal translocations between this gene and the Runx1 (AML1) gene on chromosome 21 has been observed in patients with acute myeloid leukemia. This gene was initially mapped to chromosome 14, which was later turned out to be a pseudogene. Alternatively, spliced transcript variants encoding different isoforms have been identified in this gene. [provided by RefSeq, Oct 2012].
Pyroglutamylated RFamide peptide receptor also known as orexigenic neuropeptide QRFP receptor or G-protein coupled receptor 103 (GPR103) is a protein that in humans is encoded by the QRFPR gene.
60S ribosomal protein L7a is a protein that in humans is encoded by the RPL7A gene.
Histone RNA hairpin-binding protein or stem-loop binding protein (SLBP) is a protein that in humans is encoded by the SLBP gene.
Annexin A7 is a protein that in humans is encoded by the ANXA7 gene.
General transcription factor 3C polypeptide 2 is a protein that in humans is encoded by the GTF3C2 gene.
YTH domain-containing protein 1 is a protein that in humans is encoded by the YTHDC1 gene. YTHDC1 is a nuclear protein involved in splice site selection that localises to YT bodies; dynamic subnuclear compartments, which first appear at the beginning of S-phase in the cell cycle and disperse during mitosis.
LUC7 like 3 pre-mRNA splicing factor (LUC7L3), also known as Cisplatin resistance-associated overexpressed protein, or CROP, is a human gene.
General transcription factor 3C polypeptide 1 is a protein that in humans is encoded by the GTF3C1 gene.
Protocadherin 11 X-linked, also known as PCDH11X, is a protein which in humans is encoded by the PCDH11X gene.
Transcription cofactor HES-6 is a protein that in humans is encoded by the HES6 gene.
Poly(rC)-binding protein 4 is a protein that in humans is encoded by the PCBP4 gene.
Putative RNA-binding protein 15 is a protein that in humans is encoded by the RBM15 gene. It is an RNA-binding protein that acts as a key regulator of N6-Methyladenosine (m6A) methylation of RNAs
Insulin-like growth factor 2 mRNA-binding protein 2 is a protein that in humans is encoded by the IGF2BP2 gene.
YTH domain family protein 3 is a protein that in humans is encoded by the YTHDF3 gene.
N6-adenosine-methyltransferase 70 kDa subunit (METTL3) is an enzyme that in humans is encoded by the METTL3 gene.
General transcription factor 3C polypeptide 4 is a protein that in humans is encoded by the GTF3C4 gene.
N6-Methyladenosine (m6A) was originally identified and partially characterised in the 1970s, and is an abundant modification in mRNA and DNA. It is found within some viruses, and most eukaryotes including mammals, insects, plants and yeast. It is also found in tRNA, rRNA, and small nuclear RNA (snRNA) as well as several long non-coding RNA, such as Xist.
YTH domain family, member 1 is a protein that in humans is encoded by the YTHDF1 gene.
RNA demethylase ALKBH5 is a protein that in humans is encoded by the ALKBH5 gene.
Mediator complex subunit 19 (Med19) is a protein that in humans is encoded by the MED19 gene.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.