DECIPHER is used by the clinical community to share and compare phenotypic and genotypic data. The DECIPHER database contains data from 52,412 patients who have given consent for broad data.

DECIPHER Project Proposal DECIPHER DECIPHER (DatabasE of genomiC varIation and Phenotype in Humans using Ensembl Resources) is an interactive web-based database which incorporates a suite.

Genes with Sequence Variants in DECIPHER This is a list of genes for which DECIPHER has open-access patient sequence variants, or DDD research sequence variants. These pages contain.

Understanding the Context

Decipher was developed as a tool for clinical geneticists (doctors who specialise in genetic conditions such as chromosome disorders), genetic scientists (scientists who analyse chromosomes & DNA).

DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide

Searching DECIPHER DECIPHER has an advanced search facility that allows querying the database using a combination of terms including phenotypes, gene symbols, chromosomal locations/bands.

OGG1 3:9749944-9788219 Forward strand gene: 8-oxoguanine DNA glycosylase Also known as: HMMH, HOGG1, OGH1, MUTM, ENSG00000114026 Function: DNA repair enzyme that incises DNA.

Key Insights

Collaboration DECIPHER is a tool for collating information about very rare genomic variants. Results of genomic studies, which have been undertaken either during the clinical evaluation of a patient or as.

TMEM67 8:93754844-93819234 Forward strand gene: transmembrane protein 67 Formerly known as: MKS3 Also known as: MGC26979, JBTS6, NPHP11, ENSG00000164953 Function: Required for.

TNNT2 1:201359002-201379773 Reverse strand gene: troponin T2, cardiac type Formerly known as: CMD1D, CMH2 Also known as: CMPD2, ENSG00000118194 Function: Troponin T is the.

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