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List of genes:

Gene

Gene: 

NXF2 (official gene symbol)

Other symbol: 

NXF2

CT family: 

CT39 

CT identifier: 

CT39

Aliases from NCBI:

FLJ20416 , TAPL-2

Unified entry for genes NXF2, NXF2B (nearly-identical copies)

Gene copies

NXF2 and NXF2B share 100% identity in 3 blocks (genomic region of NM_001099686). There are segments of 44 and 40 nt missing in the copy located in the plus strand. One copy is in the plus strand and the other in the minus strand.
NM_001099686 (NXF2B) and NM_017809 (NXF2) align in two blocks of 99% identity (1 mismatch in each), indicating that NM_017809 might be a splicing variant (exon skip) of NXF2, NXF2B or both. NM_022053 (NXF2) is a shorter mRNA with an extra exon.
RefSeqs as of October, 2007

RefSeq

Nucleotide : NM_022053.1 |  NM_017809.3 

Phylogenetic relationships with CT genes

This gene belongs to the NXF family.

Gene Identification

NXF2 was identified by molecular methods: search for possible orthologues of murine testis-specific gene products (Loriot et al., 2003 PMID: 12704671).

Gene structure and chromosomal localization

Chromosomal mapping data of NFX2 to Xq22.1 were retrieved from GenBank and confirmed by RH mapping (Wang et al., 2001 PMID: 11279525).

Chromosome band: Xq22.1

See this gene in the UCSC Genome Browser :

See this gene in the NCBI Map Viewer Genome Browser :

Exon-intron structure and splicing variants

    

Splicing variants documented by RefSeqs:

SNPs