Difference between revisions of "KIT"

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==Primary Author(s)*==
 
==Primary Author(s)*==
  
Put your text here
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Brian Davis PhD
  
 
__TOC__
 
__TOC__
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EXAMPLES
 
EXAMPLES
  
'''[http://atlasgeneticsoncology.org/Genes/P53ID88.html ''TP53'' by Atlas of Genetics and Cytogenetics in Oncology and Haematology]''' - detailed gene information
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'''[http://atlasgeneticsoncology.org/Genes/KITID127..html ''KIT'' by Atlas of Genetics and Cytogenetics in Oncology and Haematology]''' - detailed gene information
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'''[https://cancer.sanger.ac.uk/cosmic/gene/analysis?ln=kit ''KIT'' by COSMIC]''' - sequence information, expression, catalogue of mutations
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'''[https://civicdb.org/events/genes/29/summary/variants/66/summary ''KIT'' by CIViC]''' - general knowledge and evidence-based variant specific information
  
'''[https://cancer.sanger.ac.uk/cosmic/gene/analysis?ln=TP53 ''TP53'' by COSMIC]''' - sequence information, expression, catalogue of mutations
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'''[https://pecan.stjude.cloud/proteinpaint/kit ''KIT'' by St. Jude ProteinPaint]''' mutational landscape and matched expression data.
  
'''[https://civicdb.org/events/genes/45/summary/variants/1300/summary ''TP53'' by CIViC]''' - general knowledge and evidence-based variant specific information
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'''[https://pmkb.weill.cornell.edu/search?utf8=%E2%9C%93&search=kit ''KIT'' by Precision Medicine Knowledgebase (Weill Cornell)]''' - manually vetted interpretations of variants and CNVs
  
'''[http://p53.iarc.fr/ ''TP53'' by IARC]''' - ''TP53'' database with reference sequences and mutational landscape
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'''[http://www.cancerindex.org/geneweb/KIT.htm ''KIT'' by Cancer Index]''' - gene, pathway, publication information matched to cancer type
  
'''[https://pecan.stjude.cloud/proteinpaint/tp53 ''TP53'' by St. Jude ProteinPaint]''' mutational landscape and matched expression data.
+
'''[http://oncokb.org/#/gene/kit ''KIT'' by OncoKB]''' - mutational landscape, mutation effect, variant classification
  
'''[https://pmkb.weill.cornell.edu/search?utf8=%E2%9C%93&search=tp53 ''TP53'' by Precision Medicine Knowledgebase (Weill Cornell)]''' - manually vetted interpretations of variants and CNVs
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'''[https://www.mycancergenome.org/content/gene/kit/ ''KIT'' by My Cancer Genome]''' - brief gene overview
  
'''[http://www.cancerindex.org/geneweb/TP53.htm ''TP53'' by Cancer Index]''' - gene, pathway, publication information matched to cancer type
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'''[http://www.uniprot.org/uniprot/P10721 ''KIT'' by UniProt]''' - protein and molecular structure and function
  
'''[http://oncokb.org/#/gene/TP53 ''TP53'' by OncoKB]''' - mutational landscape, mutation effect, variant classification
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'''[http://pfam.xfam.org/protein/P10721 ''KIT'' by Pfam]''' - gene and protein structure and function information
  
'''[https://www.mycancergenome.org/content/gene/tp53/ ''TP53'' by My Cancer Genome]''' - brief gene overview
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'''[http://www.genecards.org/cgi-bin/carddisp.pl?gene=kit ''TP53'' by GeneCards]''' - general gene information and summaries
  
'''[http://www.uniprot.org/uniprot/P04637 ''TP53'' by UniProt]''' - protein and molecular structure and function
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'''[https://www.ncbi.nlm.nih.gov/gene/3815 ''KIT'' by NCBI Gene]''' - general gene information and summaries
  
'''[https://pfam.xfam.org/family/p53 ''TP53'' by Pfam]''' - gene and protein structure and function information
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'''[http://www.omim.org/entry/164920 ''KIT'' by OMIM]''' - compendium of human genes and genetic phenotypes
  
'''[http://www.genecards.org/cgi-bin/carddisp.pl?gene=tp53 ''TP53'' by GeneCards]''' - general gene information and summaries
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'''[https://databases.lovd.nl/shared/genes/kit  ''KIT'' by LOVD(3)]''' - Leiden Open Variation Database
  
'''[https://www.ncbi.nlm.nih.gov/books/NBK1311/ GeneReviews]''' - information on Li Fraumeni Syndrome
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'''[http://www.unav.es/genetica/TICdb/results.php?hgnc=kit ''KIT'' by TICdb]''' - database of Translocation breakpoints In Cancer
  
 
==References==
 
==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.
#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 ===
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2. Schafer, E.S. . et al. (2015). Molecular Genetics of Acute Lymphoblastic Leukemia in The Molecular Basis of Cancer, 4th edition. Mendelsohn, J, Howley, PM, Israel, MA, Gray, JW, Thompson, CB. Editors. Elsevier Press: Philadelphia, USA, p395-406.
#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 ==
 
== Notes ==

Revision as of 13:59, 2 August 2018

Primary Author(s)*

Brian Davis PhD

Synonyms

Put your text here

EXAMPLE: Tumor protein p53, LFS1, p53, BCC7, TRP53

Genomic Location

Cytoband: Put your text here. EXAMPLE: 17p13.1

Genomic Coordinates:

Put your text here

EXAMPLE: chr17:7,571,720-7,590,868 [hg19]

EXAMPLE: chr17:7,668,402-7,687,538 [hg38]

Cancer Category/Type

Put your text here

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

Put your text here - Include as applicable links to: 1) Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2) COSMIC, 3) CIViC, 4) St. Jude ProteinPaint, 5) Precision Medicine Knnowledgebase (Weill Cornell), 6) Cancer Index, 7) OncoKB, 8) My Cancer Genome, 9) UniProt, 10) Pfam, 11) GeneCards, 12) GeneReviews, and 13) Any gene-specific databases.

EXAMPLES

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

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

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

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

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

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

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

KIT by My Cancer Genome - brief gene overview

KIT by UniProt - protein and molecular structure and function

KIT by Pfam - gene and protein structure and function information

TP53 by GeneCards - general gene information and summaries

KIT by NCBI Gene - general gene information and summaries

KIT by OMIM - compendium of human genes and genetic phenotypes

KIT by LOVD(3) - Leiden Open Variation Database

KIT by TICdb - database of Translocation breakpoints In Cancer

References

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.

2. Schafer, E.S. . et al. (2015). Molecular Genetics of Acute Lymphoblastic Leukemia in The Molecular Basis of Cancer, 4th edition. Mendelsohn, J, Howley, PM, Israel, MA, Gray, JW, Thompson, CB. Editors. Elsevier Press: Philadelphia, USA, p395-406.

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.