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In 1991, Entrez was introduced in CD form. In 1993, a client-server version of the software provided connectivity with the internet. In 1994, NCBI established a website, and Entrez was a part of this initial release. In 2001, Entrez bookshelf was released and in 2003, the Entrez Gene database was developed. [6]
• Find the Pubmed ID of the article you want to add. Obviously, use Pubmed. • Find your favorite gene page. You can do that by searching directly here at Wikipedia (search box in the left-hand bar), and in most cases you can also find it by searching at Google or by using our Entrez Gene ID lookup tool.
A GeneRIF or Gene Reference Into Function is a short (255 characters or fewer) statement about the function of a gene. GeneRIFs provide a simple mechanism for allowing scientists to add to the functional annotation of genes described in the Entrez Gene database. In practice, function is constructed quite broadly. For example, there are GeneRIFs ...
Users can select various types of identifiers such as CCDS ID, gene ID, gene symbol, nucleotide ID and protein ID to search for specific CCDS information. [1] The CCDS reports (Figure 1) are presented in a table format, providing links to specific resources, such as a history report, Entrez Gene [10] or re-query the CCDS
The Entrez Global Query Cross-Database Search System is used at NCBI for all the major databases such as Nucleotide and Protein Sequences, Protein Structures, PubMed, Taxonomy, Complete Genomes, OMIM, and several others. [9] Entrez is both an indexing and retrieval system having data from various sources for biomedical research.
150350 383075 Ensembl ENSG00000176177 ENSMUSG00000050439 UniProt Q8IYW4 E9Q1Z2 RefSeq (mRNA) NM_152512 NM_001163189 RefSeq (protein) NP_689725 NP_001156661 Location (UCSC) Chr 22: 39.74 – 39.89 Mb Chr 15: 80.34 – 80.45 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse ENTH domain-containing protein 1, also known as Epsin-2B and ENTHD1, is a protein that in humans is encoded by the ...
DNA mismatch repair protein Mlh1 or MutL protein homolog 1 is a protein that in humans is encoded by the MLH1 gene located on chromosome 3. The gene is commonly associated with hereditary nonpolyposis colorectal cancer. Orthologs of human MLH1 have also been studied in other organisms including mouse and the budding yeast Saccharomyces cerevisiae.
This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family.Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis.