Mus musculus Gene: Aff2
Summary
InnateDB Gene IDBG-149821.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Aff2
Gene Name AF4/FMR2 family, member 2
Synonyms Fmr2; FMR2P; Ox19; Oxh
Species Mus musculus
Ensembl Gene ENSMUSG00000031189
Encoded Proteins
AF4/FMR2 family, member 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000155966:
This gene encodes a putative transcriptional activator that is a member of the AF4\FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. Fragile X E syndrome is a form of nonsyndromic X-linked mental retardation. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Dec 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome X:69360294-69868037
Strand Forward strand
Band A7.1
Transcripts
ENSMUST00000033532 ENSMUSP00000033532
ENSMUST00000139977
ENSMUST00000143097
ENSMUST00000151662
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0002151 G-quadruplex RNA binding
Biological Process
GO:0006397 mRNA processing
GO:0007611 learning or memory
GO:0008380 RNA splicing
GO:0043484 regulation of RNA splicing
Cellular Component
GO:0016607 nuclear speck
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.466576
RefSeq NM_008032 XM_006527820 XM_006527821
OMIM
CCDS CCDS30173
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas