| Name | FSHD region gene 1 family member B, pseudogene |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe recurrent dic(9;20) chromosomal abnormality in acute lymphoblastic leukemia was found to involve multiple breakpoints that disrupt several genes. In one of the newly identified rearrangements, the breakpoint mapped to sequences immediately 3′ of FRG1B (here referred to as FRG1BP), indicating that this region may be involved in the genomic disruptions observed in these leukemias. Although the study did not elaborate in detail on the normal biological function of FRG1BP, its disruption in the context of dic(9;20) translocations highlights its potential role as a candidate target locus whose alteration could contribute to leukemogenesis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}, {"type": "p", "children": [{"type": "t", "text": "\nWhile the precise physiological role of FRG1BP remains to be fully elucidated, the mapping of chromosomal breakpoints near its 3′ region suggests that its normal function might be linked to maintaining genomic integrity or regulating gene expression. The involvement of FRG1BP in these chromosomal rearrangements provides additional insight into the complex molecular architecture of acute lymphoblastic leukemia and underscores the need for further studies to understand its contribution to disease development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Qian An, Sarah L Wright, Anthony V Moorman, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Heterogeneous breakpoints in patients with acute lymphoblastic leukemia and the dic(9;20)(p11-13;q11) show recurrent involvement of genes at 20q11.21."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Haematologica (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3324/haematol.2008.002808"}], "href": "https://doi.org/10.3324/haematol.2008.002808"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19586940"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19586940"}]}]}]}
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| NCBI Gene ID | 284802 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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FRG1BP has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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If available, associations are ranked by standardized value
| Dataset | Summary |
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