The GENCODE Genes track (version 19, December 2013) shows high-quality manual
annotations merged with evidence-based automated annotations across the entire
human genome generated by the
The GENCODE gene set presents a full merge
between HAVANA manual annotation process and Ensembl automatic annotation pipeline.
Priority is given to the manually curated HAVANA annotation using predicted
Ensembl annotations when there are no corresponding manual annotations.
The annotation was carried out on genome assembly GRCh37 (hg19).
As of GENCODE Version 11, Ensembl and GENCODE have converged. The gene
annotations in the GENCODE comprehensive set are the same as the corresponding
Ensembl release. UCSC will continue to provide a separate Ensembl track on
Human in the same format as the Ensembl tracks on other organisms.
NOTE: Due to the UCSC Genome Browser using the NC_001807 mitochondrial
genome sequence (chrM) and GENCODE annotating the NC_012920 mitochondrial
sequence, the GENCODE mitochondrial annotations have been lifted to NC_001807
coordinates in the UCSC Genome Browser. The original annotations with
NC_012920 coordinates are available for download in the GENCODE GTF files.
Display Conventions and Configuration
This track is a multi-view composite track that contains differing data sets
(views). Instructions for configuring multi-view tracks are
To show only selected subtracks, uncheck the boxes next to the tracks that
you wish to hide.
Views available on this track are:
The gene annotations in this view are divided into three subtracks:
GENCODE Basic set is a subset of the Comprehensive set.
The selection criteria are described in the methods section.
GENCODE Comprehensive set contains all GENCODE coding and non-coding transcript annotations,
including polymorphic pseudogenes. This includes both manual and
automatic annotations. This is a super-set of the Basic set.
GENCODE Pseudogenes include all annotations except polymorphic pseudogenes.
GENCODE 2-way Pseudogenes contains pseudogenes predicted by both the Yale
Pseudopipe and UCSC Retrofinder pipelines.
The set was derived by looking for 50 base pairs
of overlap between pseudogenes derived from both sets based on their
chromosomal coordinates. When multiple Pseudopipe
predictions map to a single Retrofinder prediction, only one match is kept
for the 2-way consensus set.
GENCODE PolyA contains polyA signals and sites manually annotated on
the genome based on transcribed evidence (ESTs and cDNAs) of 3' end of
transcripts containing at least 3 A's not matching the genome.
Filtering is available for the items in the GENCODE Basic, Comprehensive and Pseudogene tracks
using the following criteria:
Transcript class: filter by the basic biological function of a transcript
All - don't filter by transcript class
coding - display protein coding transcripts, including polymorphic pseudogenes
Coloring for the gene annotations is based on the annotation type:
all 2-way pseudogenes
all polyA annotations
The GENCODE project aims to annotate all evidence-based gene features on the
human reference sequence with high accuracy by integrating
computational approaches (including comparative methods), manual
annotation and targeted experimental verification. This goal includes identifying
all protein-coding loci with associated alternative variants, non-coding
loci which have transcript evidence, and pseudogenes.
For a detailed description of the methods and references used, see
Harrow et al. (2006).
GENCODE Basic Set selection:
The GENCODE Basic Set is intended to provide a simplified subset of
the GENCODE transcript annotations that will be useful to the majority of
users. The goal was to have a high-quality basic set that also covered all loci.
Selection of GENCODE annotations for inclusion in the basic set
was determined independently for the coding and non-coding transcripts at each
Criteria for selection of coding transcripts (including polymorphic pseudogenes) at a given
All full-length coding transcripts (except problem transcripts or transcripts that are
nonsense-mediated decay) were included in the basic set.
If there were no transcripts meeting the above criteria, then the partial coding
transcript with the largest CDS was included in the basic set (excluding problem transcripts).
Criteria for selection of non-coding transcripts at a given locus:
All full-length non-coding transcripts (except problem transcripts)
with a well characterized biotype (see below) were included in the
If there were no transcripts meeting the above criteria, then the largest non-coding
transcript was included in the basic set (excluding problem transcripts).
It no transcripts were included by either the above criteria, the longest
problem transcript is included.
Non-coding transcript categorization:
Non-coding transcripts are categorized using
and the following criteria:
well characterized: antisense, Mt_rRNA, Mt_tRNA, miRNA, rRNA, snRNA, snoRNA
Transcription Support Level (TSL):
It is important that users understand how to assess transcript annotations
that they see in GENCODE. While some transcript models have a high level of
support through the full length of their exon structure, there are also
transcripts that are poorly supported and that should be considered
speculative. The Transcription Support Level (TSL) is a method to highlight the
well-supported and poorly-supported transcript models for users. The method
relies on the primary data that can support full-length transcript
structure: mRNA and EST alignments supplied by UCSC and Ensembl.
The mRNA and EST alignments are compared to the GENCODE transcripts and the
transcripts are scored according to how well the alignment matches over its
The GENCODE TSL provides a consistent method of evaluating the
level of support that a GENCODE transcript annotation is
actually expressed in humans. Human transcript sequences from the
Sequence Database Collaboration (GenBank, ENA, and DDBJ) are used as
the evidence for this analysis.
Exonerate RNA alignments from Ensembl,
BLAT RNA and EST alignments from the UCSC Genome Browser Database are used in
the analysis. Erroneous transcripts and libraries identified in lists
maintained by the Ensembl, UCSC, HAVANA and RefSeq groups are flagged as
suspect. GENCODE annotations for protein-coding and non-protein-coding
transcripts are compared with the evidence alignments.
Annotations in the MHC region and other immunological genes are not
evaluated, as automatic alignments tend to be very problematic.
Methods for evaluating single-exon genes are still being developed and
they are not included
in the current analysis. Multi-exon GENCODE annotations are evaluated using
the criteria that all introns are supported by an evidence alignment and the
evidence alignment does not indicate that there are unannotated exons. Small
insertions and deletions in evidence alignments are assumed to be due to
polymorphisms and not considered as differing from the annotations. All
intron boundaries must match exactly. The transcript start and end locations
are allowed to differ.
The following categories are assigned to each of the evaluated annotations:
tsl1 - all splice junctions of the transcript are supported by
at least one non-suspect mRNA
tsl2 - the best supporting mRNA is flagged as suspect or the support is from multiple ESTs
GSE34821:[E-MTAB-831] - Batch VI is based on annotations from GENCODE 6 (November 2010) as well as transcript models predicted by the Ensembl Genebuild group based on the Illumina Human BodyMap 2.0 data.
See Harrow et al. (2006) for information on verification
GENCODE version 19 corresponds to Ensembl 74 and Vega 54.
Jennifer Harrow, Timothy Cutts, Bronwen Aken, James Gilbert, Jyoti Choudhary, Ed Griffiths, Jose Manuel Gonzalez, Electra Tapanari, Daniel Barrell, Adam Frankish, Andrew Berry, Alexandra Bignell, Veronika Boychenko, Claire Davidson, Gloria Despacio-Reyes, Mike Kay, Deepa Manthravadi, Gaurab Mukherjee, Catherine Snow, Gemma Barson, Matt Hardy, Joanne Howes