Contents
The CGD locus page is divided into three sections: BASIC
INFORMATION, RESOURCES, and ADDITIONAL INFORMATION, as described below.
The Basic Information section lists any names and aliases (synonyms, including allele names) for a
particular locus, and indicates whether a name is standard or
reserved. Additional information about gene names in CGD (including explanation of the standard format, systematic name format, and other gene identifiers used) may be found on the Nomenclature page. The Basic Information Section also includes the following additional information:
Please note, regarding the issue of orthology and shared function:
A detailed description of the methodology used to generate the
ortholog and best hit mappings is posted here.
As described here, the evidence code "ND", or "Not Determined" is used with annotations to the three root terms "molecular_function unknown", "biological_process unknown", or "cellular_component unknown" and signifies that a curator has examined the literature and that as of the date of the annotation to the unknown term, there were either no publications concerning that gene, or there was no information in any available publications that allowed a curator to make an annotation to a specific term in that ontology.
page).
Basic Information
A concise summary of the biological role and molecular function of
the gene, and any other particularly salient information. Genes
without experimental characterization may have descriptions that
discuss orthology to genes in other organisms, as described in more
detail.
This section provides ortholog and best hit mappings.
We use the standard evolutionary definition of orthology: genes
descended from a common ancestral gene sequence. This definition does
not require that the genes are functionally equivalent after the
speciation event, although it will often be the case.
The GO annotations describe a gene's molecular functions, its role
in biological processes, and its presence in cellular components or
complexes. Each annotation links to a page showing all genes
annotated to the term in CGD. The GO annotations use a controlled vocabulary
that allow powerful searches within CGD and across other
databases. The "Gene Ontology" tab and the "GO evidence and
references" link will display a page with more information about the
GO assignments, including links to the references that support
assignment of each GO term.
The Phenotype field lists the mutant
phenotype for the gene. The "Phenotype" tab and "Phenotype details
and references" links display a page with additional information about the phenotypes, including references and additional notes.
The Pathways field lists any biochemical
pathways in which the gene product is predicted to participate. Each
pathway name is hyperlinked to the corresponding pathway diagram.
The Sequence Information field
indicates the location of the gene in the genome. The coordinates of each exon and
intron are listed, with the relative position of these regions with
respect to the feature, and to the chromosome. Also displayed are the dates on which the
most recent updates to the sequence coordinates and to the sequence
itself were made. Dates that appear on many C. albicans pages:
Please note: Gaps
have been introduced into some ORFs to make adjustments to the reading
frame or to eliminate stop codons, in cases in which the annotator
judged that the sequence was likely to be in error. These gaps called
"Adjustments," rather than "Introns" on the Locus page of the affected
ORFs in Assembly 21. (All introns and adjustments are called
"Gaps" in Assembly 19.) Some of the gaps have a length that is a
negative number; that is, the coding sequence comprises two
overlapping segments, such that some sequence is counted twice. The
"adjustments" should be considered flags that indicate that
resequencing of the area is advised.
The Contig Location field lists the name of the contig (in Contig19 nomenclature, from Assembly 19 of the genomic sequence) and the base pair coordinates within the contig at which each allele resides. The name of each allele is a hyperlink to the GBrowse genome browser, which allows viewing and navigation of the contig.
This field provides links to other information sources for the gene.
This is an identifier that has been
assigned to the locus at CGD. Resources
Allows you to view and
navigate chromosome or contig sequences. GBrowse may be accessed
using the GBrowse map thumbnail views or the links in the Sequence
Information section. See the C. albicans ACT1 Locus Page as an example. The three small maps on the right-hand side of the page correspond to the ACT1 ORF in Assembly 21 and, below, the two ACT1 alleles from Assembly 19. Clicking on one of these will display a region of the chromosome or contig, with the selected ORF at the center and neighboring ORFs visible on either side. GBrowse is described in more detail on the GBrowse Help Documentation page.
Retrieves, for the gene in Assembly 21, or for each allele in
Assembly 19, the Genomic DNA (with introns), the Exons-only Sequence
(Coding Sequence of an ORF, or the sequence with exons removed of any
non-translated feature) , the Genomic DNA with 1 kb of flanking sequence upstream and downstream of the gene (also includes any introns), or the ORF
translation. For more details about the sequence datasets, please see
the Sequence Documentation
page.
Sequences are displayed by default in FASTA format. Several
other sequence formats are available as hyperlinks on the page displaying
the sequence, or via the Gene/Seq
Resources tool. The other formats include, GCG, No
header, Decorated FASTA and Numbered sequence.
Allow comparison of the genomic, coding, or ORF translation sequence
to various C. albicans sequence datasets. For more detailed
instructions for use of the BLAST tool, please see the BLAST Search Help page. For a detailed
description of the search output, please see the BLAST Results Help page.
Recommends primers appropriate for either PCR or sequencing of a
given sequence, within configurable parameters. For more
information about this tool, please see the Web Primer
tool help page.
Generates a restriction map of a specified DNA sequence. The
restriction map may include all enzymes, or a subset of enzyme
types (3' overhangs, 5' overhangs, blunt ends, or enzymes that cut
once or twice). For more
information about this tool, please see the Restriction Analysis tool help page.
The Flanking Features Table
provides a tabular view of the other nearby features (ORFs, etc.) on
the Assembly 21 chromosome, with brief descriptions of each
neighboring feature and links to additional resources and
information. By default, the table lists features within 5 kb flanking
the locus; use the "Retrieve Features Left" or "Retrieve Features
Right" options near the bottom of the page to include additional
flanking region. The column labeled "Retrieve" provides links to the
Locus page and to the Assembly 21 nucleotide sequence of each feature
listed in the table.
Documentation
Additional Information
Locus Summary Notes
References Cited on this Page
Return to CGD | Send a Message to the CGD Curators |