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THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 11th,2023. The database HOX Pro contains information about organization, functions and evolution of gene ensembles, key roles in which play homeobox-genes. It is aimed at: 1. analysis and classification of regulatory and coding regions in diverse homeobox and related genes; 2. describing mutations and knock-outs of hox-genes, as well as hereditary diseases related to these genes; 3. graphical representation, comparisons and classification of hox-genes expression patterns and profiles (sea urchin blastula, Drosophila blastoderm and imaginal discs, vertebrate limbs, mammalian brain, human EC cells); 4. comparative analysis of organization of hox-based genetic networks the nematode Caenorhabditis elegans the sea urchins Strongylocentrotus purpuratus and other echinids, the fruit flies Drosophila melanogaster and D.virilis, the vertebrates chicken and mouse; 5. analysis of phylogeny and evolution of homeobox genes and clusters.

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• SciCrunch
• 17 years ago - by Anonymous

HumHot is a collection of human meiotic hot spots obtained from the literature along with interesting information on meiotic recombination and molecular features of meiotic hot spots. It is also updated as more hot spots get discovered in the human genome. The database can be queried by hot spot name or chromosome number.

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• SciCrunch
• 17 years ago - by Anonymous

THIS RESOURCE IS NO LONGER IN SERVICE, documented on July 15, 2013. A database system for retrieve human genome information in different data sources that are available to public. The information you could find here is automatically extracted from the genetic databases and shown with all data having the identifiers in common and linking to one another. HOWDY facilitates obtaining information of human genes by using official symbols and aliases approved by HGNC, GDB and Entrez Gene. It also provides a graphical view of the Human Genome maps for the finished contigs as well as radiation hybrid maps.

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• SciCrunch
• 17 years ago - by Anonymous

It provides information about the evolutionary history of the residues on the interface and represents which residues are highly conserved on the interface. In this way, functionally and structurally important residues on the interface can be distinguished. Hotsprint contains overall properties of the interface such as number of computational hot spots on the interface, number of conserved residues on the interface, average conservation score of interface residues and buried ASA of the interface. Additionally, residues of the interface along with their position, name, conservation score, ASA in monomer, ASA in complex, type (contacting interface residue, neighboring interface residue or none) and whether the residue is computational hot spot or not information are presented.

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• SciCrunch
• 17 years ago - by Anonymous

HORDE (The Human Olfactory Data Explorer) is a database of human Olfactory Receptors (ORs), the largest multigene family in multicellular organisms. You will find here information on the OR proteins, their gene structure and their genomic organization. Also available are OR repertoires of other mammalian species, along with a set of analysis tools. human olfactory receptor, :OR, OR proteins, olfactory receptor, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

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• SciCrunch
• 17 years ago - by Anonymous

Hoppsigen is a nucleic database of homologous processed pseudogenes. It contains 5,823 human retroelements and 3,934 mouse retroelements. These retroelements were annotated and stored in the database HOPPSIGEN (Homologous processed pseudogenes). Sequences were grouped in families considering their homologies. The database contains 3,168 families of exclusively human (1,966) or mouse retroelements (1,202) and 323 families containing human and mouse retroelements. 5,206 human retroelements were annotated as processed pseudogenes (respectively 3,428 mouse retroelements). The database contains functional genes from ENSEMBL homologous to Hoppsigen retroelements.

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• SciCrunch
• 17 years ago - by Anonymous

THIS RESOURCE IS NO LONGER IN SERVICE, documented on June 23, 2013. Homophila utilizes the sequence information of human disease genes from the NCBI OMIM (Online Mendelian Inheritance in Man) database in order to determine if sequence homologs of these genes exist in the current Drosophila sequence database (FlyBase). Sequences are compared using NCBI's BLAST program. The database is updated weekly and can be searched by human disease, gene name, OMIM number, title, subtitle and/or allelic variant descriptions.

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• SciCrunch
• 17 years ago - by Anonymous

A database of homologous invertebrate genes, structured under ACNUC sequence database management system. It allows one to select sets of homologous genes among invertebrate species, and to visualize multiple alignments and phylogenetic trees. The database itself contains all invertebrate protein sequences from UniProt (SWISS-PROT+TrEMBL), with some data corrected, clarified or completed (notably to address the problem of redundancy and orthology/paralogy) and with some annotation modifications. It contains also all the corresponding nucleotide sequences in EMBL. Homologous proteins are classified into families and multiple alignments and phylogenetic trees are computed for each family. Sequences and related information have been structured in an ACNUC database. Thus, HOINVGEN is particularly useful for comparative sequence analysis, phylogeny and molecular evolution studies. More generally, HOINVGEN gives an overall view of what is known about a peculiar gene family.

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• SciCrunch
• 17 years ago - by Anonymous

THIS RESOURCE IS NO LONGER IN SERVICE, documented on July 16, 2013. It provides access to the results of tests for positive selection in 14,000 human genes. Multiple alignments of protein-coding regions of genes from human and other mammals were extracted from whole-genome alignments available from UC-Santa Cruz. Each gene was analyzed using the maximum likelihood tests of selection using PAML. Branch, site, and branch+site tests were performed, each with at least one matching null model.

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• SciCrunch
• 17 years ago - by Anonymous

THIS RESOURCE IS NO LONGER IN SERVICE, documented on July 16, 2013. A database of biochemical compound information. All files are available for download, and all entries are cataloged by accession number. Klotho is part of a larger attempt to model biological processes, beginning with biochemistry.

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• SciCrunch
• 17 years ago - by Anonymous

A human mitochondrial resource aimed at supporting population genetics and mitochondrial disease studies. It consists of a database of Human Mitochondrial Genomes annotated with population and variability data, the latter estimated through the application of a new approach based on site-specific nucleotidic and aminoacidic variability calculation (SiteVar and MitVarProt programs). The goals of HmtDB are: to collect and integrate the publicly available human mitochondrial genomes data; to produce and provide the scientific community with site-specific nucleotidic and aminoacidic variability data estimated on all the collected human mitochondrial genome sequences; to allow any researcher to analyse his own human mitochondrial sequences (both complete and partial mitochondrial genomes) in order to automatically detect the nucleotidic variants compared to the revised Cambridge Reference Sequence (rCRS) and to predict their haplogroup paternity. HmtDBs first release contains 1255 human mitochondrial genomes derived from public databases (GenBank and MitoKor). The genomes have been stored and analysed as a whole dataset and grouped in continent-specific subsets (AF: Africa, AM: America, AS: Asia, EU: Europe, OC: Oceania). :The multialignment and site-variability analysis tools included in HmtDB are clustered in two Work Flows: the Variability Generation Work Flow (VGWF) and the Classification Work Flow (CWF), which are applied both to human mitochondrial genomes stored in the database and to newly sequenced genomes submitted by the user, respectively., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

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• SciCrunch
• 17 years ago - by Anonymous

Curated collection of human metabolite and human metabolism data which contains records for endogenous metabolites, with each metabolite entry containing detailed chemical, physical, biochemical, concentration, and disease information. This is further supplemented with thousands of NMR and MS spectra collected on purified reference metabolites.

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• SciCrunch
• 14 years ago - by Anonymous

Histone Database is a database of histones and their corresponding sequences. Sequence- and text-based searches were performed on NCBI's redundant and non-redundant (nr) peptide sequence databases. These databases are derived from GenBank, EMBL, and DDBJ translated DNA coding regions, plus protein sequences from the PDB (Protein Data Bank), SWISS-PROT, the PIR (Protein Information Resource), and the PRF (Protein Research Foundation). :Users can search by keyword, sequence fragment, category, organism, and redundancy of the set.

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• SciCrunch
• 17 years ago - by Anonymous

HIC-Up, the Hetero-compound Information Centre - Uppsala, a freely accessible resource for structural biologists who are dealing dealing with hetero-compounds ("small molecules"). This site contains information about hetero-compounds encountered in files from the Protein Data Bank (PDB). For every compound, a subset of the following information is available: Coordinate files (PDB and text files) Visualisation files (Chime and VRML) Dictionary files (X-PLOR/CNS, O, TNT) Links to off-site databases and servers (PDBsum, EDS, PRODRG, Relibase, MSDchem, ChemDB, Jena HCD, etc.) Miscellaneous files and information

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• SciCrunch
• 17 years ago - by Anonymous

Publicly available database of summary level findings from genetic association studies in humans, including genome wide association studies (GWAS). Previously named HGBASE, HGVbase and HGVbaseG2P.

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• SciCrunch
• 17 years ago - by Anonymous

Allow the high-performance display of next-generation sequencing experiment results in the UCSC Genome Browser.

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• SciCrunch
• 13 years ago - by Anonymous

Kinomer is a multilevel HMM library that models these protein kinase groups. It allows accurate identification of protein kinases and classification to the appropriate kinase group. Profile hidden Markov models (HMMs) are statistical descriptions of sequence conservation from multiple sequence alignments, and have been shown to outperform standard pairwise sequence comparison methods, both in terms of sensitivity and specificity. HMMs form the basis of protein family and domain description libraries such as SUPERFAMILY and Pfam.

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• SciCrunch
• 17 years ago - by Anonymous

The Horizontal Gene Transfer DataBase (HGT-DB) is a genomic database that includes statistical parameters such as G+C content, codon and amino-acid usage, as well as information about which genes deviate in these parameters for prokaryotic complete genomes. Under the hypothesis that genes from distantly related species have different nucleotide compositions, these deviated genes may have been acquired by horizontal gene transfer.

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• SciCrunch
• 17 years ago - by Anonymous

HepSEQ is the International Repository for Hepatitis B Virus Strain Data. It is web-accessible, quality-based, molecular, clinical and epidemiological database for hepatitis B infection and provides a tool for the research community or for those involved in hepatitis B case management. This database currently has 1012 patient records and 1253 viral sequences. The quality of all submitted sequences is checked. The tools provided include: SeqMatch: search the database for matching sequences Genotyper: genotype HBV strains (based on HBV surface antigen genes) Gene Mutation: display the sequences that contain mutations in HBV coding regions Mutation Annotator: annotate sequences for mutation known to be associated with anti-viral resistance This web database development is funded by the UK Department of Health is curated and is hosted by the Health Protection Agency.

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• SciCrunch
• 17 years ago - by Anonymous

Genomic database that includes prediction of which genes are highly expressed in prokaryotic complete genomes under strong translational selection.

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• SciCrunch
• 17 years ago - by Anonymous