Large deletions in human brca1 gene and use thereof

a technology of human brca1 and large deletion, applied in the field of human genetics, can solve problems such as significant alterations in structure or biochemical activities

Inactive Publication Date: 2008-12-25
MYRIAD GENETICS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

These large deletions are believed to be deleterious and cause significant alterations in structure or biochemical activities in the BRCA1 gene products expressed from mutant BRCA1 genes.

Method used

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  • Large deletions in human brca1 gene and use thereof
  • Large deletions in human brca1 gene and use thereof
  • Large deletions in human brca1 gene and use thereof

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Embodiment Construction

1. Definitions

[0023]The terms “genetic variant,”“mutation,” and “nucleotide variant” are used herein interchangeably to refer to changes or alterations to a reference BRCA1 gene sequence at a particular locus, including, but not limited to, nucleotide base deletions, insertions, inversions, and substitutions in the coding and noncoding regions. Deletions may be of a single nucleotide, a portion or a region of the nucleotide sequence of the gene, or of the entire gene sequence. Insertions may be of one or more nucleotides. The genetic variants may occur in transcriptional regulatory regions, untranslated regions of mRNA, exons, introns, or exon / intron junctions. The genetic variants may or may not result in stop codons, frame shifts, deletion of amino acids, altered amino acid sequence, or altered protein expression level. The mutations or genetic variants can be somatic, i.e., occur only in certain tissues of the body and are not inherited in the germline, or germline mutations, i.e...

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Abstract

Large deletions have been identified in the BRCA1 gene in patients. The large deletions predispose the patients to breast cancer and ovarian cancer. Thus, methods for detecting the genetic variants are provided which can be used in detecting a predisposition to cancer.

Description

CROSS-REFERENCE TO RELATED U.S. APPLICATIONS[0001]This application is a Divisional of U.S. patent application Ser. No. 10 / 457,839 filed on Jun. 9, 2003, expected to issue on Jul. 31, 2007 as U.S. Pat. No. 7,250,497; which claims the benefit (under 35 U.S.C. § 119(e)) of U.S. Provisional Application Nos. 60 / 387,132 filed on Jun. 7, 2002 and 60 / 402,430 filed on Aug. 9, 2002; all of which are incorporated by reference herein in their entirety.SEQUENCE LISTING[0002]The instant application was filed with a formal Sequence Listing submitted electronically as a text file. This text file, which was named “3002-01-12D-2007-07-30-SEQ-LST-JBO_ST25”, was created on Jul. 30, 2007, and is 15,974 bytes in size. Its contents are incorporated by reference herein in their entirety.TECHNICAL FIELD OF THE INVENTION[0003]This invention generally relates to human genetics, particularly to the identification of genetic polymorphic variations in the human BRCA1 gene and methods of using the identified gene...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12Q1/68G01N33/53C12Q
CPCC12Q1/6886C12Q2600/156C12Q2600/136
Inventor SCHOLL, THOMASHENDRICKSON, BRANT C.WARD, BENJAMINPRUSS, DMITRY
Owner MYRIAD GENETICS
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