FRAXD: Difference between revisions
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[[Category:Genes on human chromosome X]] | [[Category:Genes on human chromosome X]] | ||
[[Category:Proteins]] | [[Category:Proteins]] |
Latest revision as of 21:44, 13 January 2019
NCBI genome ID | 2480 |
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Ploidy | Diploid |
Number of chromosomes | X |
FRAXD or FRAXD gene is a gene symbol for fragile site, aphidicolin type, common, fra(X)(q27.2) D. The locus of the gene is located on fragile site of the q arm of chromosome X at position 27.2. It is used for gene testing in Homo sapiens (Human beings).[1][2][3]
References
- ↑ "FRAXD Symbol Report - HUGO Gene Nomenclature Committee". www.genenames.org.
- ↑ "FRAXD fragile site, aphidicolin type, common, fra(X)(q27.2) D [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov.
- ↑ "FRAXD gene cDNA ORF clone, Homo sapiens(human) - GenScript". www.genscript.com.
This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it. |