YTHDF2

GENERAL INFORMATION

? »

Gene name

YTHDF2

Gene description

YTH domain family, member 2

Protein class

Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Normal tissues displayed moderate to strong nuclear staining. Skeletal muscle cells, parathyroid, bile duct and most mesenchymal cells were weakly stained or negative.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA059621
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

? »

Gene name

YTHDF2 (HGNC Symbol)

Synonyms

HGRG8, NY-REN-2

Description

YTH domain family, member 2 (HGNC Symbol)

Entrez gene summary

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. In addition, 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]

Chromosome

1

Cytoband

p35.3

Chromosome location (bp)

28736621 - 28769775

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000198492 (version 78.38)

Entrez gene

51441

UniProt

Q9Y5A9 (UniProt - Evidence at protein level)

neXtProt

NX_Q9Y5A9

Antibodypedia

YTHDF2 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000373812
 
ENST00000474884
 
ENST00000496288
 
ENST00000541996
 
ENST00000542507
 
ENST00000621244
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

YTHDF2-001 ENSP00000362918
ENST00000373812
Q9Y5A9
Show all »
Show » Show » 579 62.3 No 0
YTHDF2-003 ENSP00000474446
ENST00000474884
S4R3J8
Show all »
Show » 200 21 No 0
YTHDF2-006 ENSP00000474784
ENST00000496288
S4R3V3
Show all »
Show » 241 24.9 No 0
YTHDF2-008 ENSP00000439394
ENST00000541996
Q9Y5A9
Show all »
Show » Show » 529 56.9 No 0
YTHDF2-201 ENSP00000444660
ENST00000542507
Q9Y5A9
Show all »
Show » Show » 579 62.3 No 0
YTHDF2-202 ENSP00000481408
ENST00000621244
B5BU99
Show all »
Show » 569 61.2 No 0