Difference between revisions of "FGFR1"

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Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1
 
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1
  
According to "WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues", blah, blah.
+
According to "WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues",
 +
"...clinical and morphologic presentations associated with FGFR1 rearrangement are variable, and include not only presentation as a myeloproliferative neoplasm with eosinophilia, but also as AML and they may even present as, or evolve to, precursor T or B lymphoblastic leukaemia/lymphoma with prominent eosinphils." (p.28).
 +
 
 +
FGFR1 rearrangements are used to rule out diagnoses of Chronic Eosinophilic Leukaemia (p.54) and Myeloproliferative neoplasm,unclassifiable (p.66).
 +
 
 +
In the case of FGFR1-related disease,
 +
a lymphomatous presentation is common,
 +
particularly T-LBL with accompanying eosinophilia. Other patients have had CEL,
 +
precursor-B lymphoblastic leukaemia/
 +
lymphoma or AML. (.70).
  
 
==Gene Overview==
 
==Gene Overview==

Revision as of 15:35, 11 October 2018

Primary Author(s)*

Brian Davis PhD

Synonyms

"Fibroblast Growth Factor Receptor 1"; "Basic Fibroblast Growth Factor Receptor 1"; BFGFR; "Heparin-Binding Growth Factor Receptor "; HBGFR; "Fms-Related Tyrosine Kinase 2"; "Fms-Like Tyrosine Kinase 2"; FLT2; CEK; FLG; CD331; ECCL; KAL2

Genomic Location

Cytoband: 8p11.23

Genomic Coordinates:

chr8:38,411,138-38,468,834 [hg38]

chr8:38,268,656-38,326,352 [hg19]

Cancer Category/Type

Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1

According to "WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues", "...clinical and morphologic presentations associated with FGFR1 rearrangement are variable, and include not only presentation as a myeloproliferative neoplasm with eosinophilia, but also as AML and they may even present as, or evolve to, precursor T or B lymphoblastic leukaemia/lymphoma with prominent eosinphils." (p.28).

FGFR1 rearrangements are used to rule out diagnoses of Chronic Eosinophilic Leukaemia (p.54) and Myeloproliferative neoplasm,unclassifiable (p.66).

In the case of FGFR1-related disease, a lymphomatous presentation is common, particularly T-LBL with accompanying eosinophilia. Other patients have had CEL, precursor-B lymphoblastic leukaemia/ lymphoma or AML. (.70).

Gene Overview

Put your text here.

Common Alteration Types

Put your text here and/or fill in the table with an X where applicable

Copy Number Loss Copy Number Gain LOH Loss-of-Function Mutation Gain-of-Function Mutation Translocation/Fusion
EXAMPLE: X EXAMPLE: X EXAMPLE: X EXAMPLE: X EXAMPLE: X EXAMPLE: X

Internal Pages

Put your text here

EXAMPLE Germline Cancer Predisposition Genes

External Links

FGFR1 by Atlas of Genetics and Cytogenetics in Oncology and Haematology - detailed gene information

FGFR1 by COSMIC - sequence information, expression, catalogue of mutations

FGFR1 by CIViC - general knowledge and evidence-based variant specific information

FGFR1 by St. Jude ProteinPaint mutational landscape and matched expression data.

FGFR1 by Precision Medicine Knowledgebase (Weill Cornell) - manually vetted interpretations of variants and CNVs

FGFR1 by Cancer Index - gene, pathway, publication information matched to cancer type

FGFR1 by OncoKB - mutational landscape, mutation effect, variant classification

FGFR1 by NCBI Gene - brief gene overview

FGFR1 by My Cancer Genome - brief gene overview

FGFR1 by UniProt - protein and molecular structure and function

FGFR1' by Pfam - gene and protein structure and function information

FGFR1 by GeneCards - general gene information and summaries

FGFR1 by OMIM - compendium of human genes and genetic phenotypes

FGFR1' by LOVD(3) - Leiden Open Variation Database

FGFR1 by TICdb - database of Translocation breakpoints In Cancer

References

EXAMPLE Book

  1. Arber DA, et al., (2008). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th edition. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW, Editors. IARC Press: Lyon, France, p117-118.

EXAMPLE Journal Article

  1. Li Y, et al., (2001). Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia. Nat Genet 28:220-221, PMID 11431691.

Notes

*Primary authors will typically be those that initially create and complete the content of a page. If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage). Additional global feedback or concerns are also welcome.