The NCBI RefSeq Genes composite track shows human protein-coding and non-protein-coding
genes taken from the NCBI RNA reference sequences collection (RefSeq). All subtracks use
coordinates provided by RefSeq, except for the UCSC RefSeq, which UCSC produces by
realigning the RefSeq RNAs to the genome. This realignment may result in occasional differences
between the annotation coordinates provided by UCSC and NCBI. See the
Methods section for more details about how the different tracks were
Please visit NCBI's Feedback for Gene and Reference Sequences (RefSeq) page to make suggestions,
submit additions and corrections, or ask for help concerning RefSeq records.
Display Conventions and Configuration
This track is a multi-view composite track that contains differing data set views.
Instructions for configuring multi-view tracks are
To show only a selected set of subtracks, uncheck the boxes next to the tracks that you wish to
The views available for this track include:
- RefSeq annotations and alignments
RefSeq All – all curated and predicted annotations provided by
RefSeq Curated – subset of RefSeq All that includes only those
annotations whose accessions begin with NM, NR, or YP.
RefSeq Predicted – subset of RefSeq All that includes those annotations whose
accessions begin with XM or XR.
RefSeq Other – all other annotations produced by the RefSeq group that
do not fit the requirements for inclusion in the RefSeq Curated or the
RefSeq Predicted tracks.
RefSeq Alignments – alignments of RefSeq RNAs to the human genome provided
by the RefSeq group.
- UCSC annotations
UCSC RefSeq – annotations generated from UCSC's realignment of RNAs with NM
and NR accessions to the human genome. This track was previously known as the "RefSeq
The RefSeq All, RefSeq Curated, RefSeq Predicted and UCSC RefSeq
tracks follow the display conventions for
gene prediction tracks.
The color shading indicates the level of review the RefSeq record has undergone:
predicted (light), provisional (medium), or reviewed (dark).
The RefSeq Alignments track follows the display conventions for
The item labels and codon display properties for features within this track can be configured
through the controls at the top of the track description page. Click the view name
(NCBI RefSeq or UCSC RefSeq) to globally modify the settings for all subtracks in
the view. To adjust the settings for an individual subtrack, click the wrench icon next to the
track name in the subtrack list (available only for views containing more than one track).
Label: By default, items are labeled by gene name. Click the appropriate Label
option to display the accession name or OMIM identifier instead of the gene name, show all or a
subset of these labels including the gene name, OMIM identifier and accession names, or turn off
the label completely.
Codon coloring: This track has an optional codon coloring feature that
allows users to quickly validate and compare gene predictions. To display codon colors, select the
genomic codons option from the Color track by codons pull-down menu. For more
information about this feature, go to the Coloring Gene Predictions and Annotations by Codon page.
Tracks contained in the RefSeq annotation and RefSeq RNA alignment views were created at UCSC using
data from the NCBI RefSeq project. Data files were downloaded from RefSeq in GFF file format and
converted to the genePred and PSL table formats for display in the Genome Browser. Information about
the NCBI annotation pipeline can be found
The UCSC RefSeq Genes track is constructed using the same methods as previous RefSeq Genes tracks.
RefSeq RNAs were aligned against the human genome using BLAT. Those with an alignment of
less than 15% were discarded. When a single RNA aligned in multiple places, the alignment
having the highest base identity was identified. Only alignments having a base identity
level within 0.1% of the best and at least 96% base identity with the genomic sequence were
The raw data for these tracks can be accessed in multiple ways. It can be explored interactively
using the Table Browser or
Data Integrator. The tables can also be accessed
programmatically through our
public MySQL server or downloaded from our
downloads server for local
The data in the RefSeq Other track is organized in a
bigBed file format; more
information about accessing the information in this bigBed file can be found
below. The other subtracks are associated with database tables as follows:
- genePred format:
- RefSeq All - ncbiRefSeq
- RefSeq Curated - ncbiRefSeqCurated
- RefSeq Predicted - ncbiRefSeqPredicted
- UCSC RefSeq - refGene
- PSL format:
- RefSeq Alignments - ncbiRefSeqPsl
The first column of each of these tables is "bin". This column is designed
to speed up access for display in the Genome Browser, but can be safely ignored in downstream
analysis. You can read more about the bin indexing system
The annotations in the RefSeq Other track are stored in a bigBed file,
ncbiRefSeqOther.bb, that can be obtained from our downloads server
Individual regions or the whole set of genome-wide annotations can be obtained using our tool
bigBedToBed which can be compiled from the source code or downloaded as a precompiled
binary for your system from the utilities directory linked above. For example, to extract only
annotations in a given region, you could use the following command:
-chrom=chr16 -start=34990190 -end=36727467 stdout
The genePred format tracks can also be downloaded in GTF format using the
genePredToGtf utility, available from the
utilities directory on the UCSC downloads
server. The utility can be run from the command line like so:
genePredToGtf hg38 ncbiRefSeqPredicted ncbiRefSeqPredicted.gtf
Note that using genePredToGtf in this manner accesses our public MySQL server, and you therefore
must set up your hg.conf as described on the MySQL page linked near the beginning of the Data Access
A file containing the RNA sequences in FASTA format for all items in the RefSeq All, RefSeq Curated,
and RefSeq Predicted tracks can be found on our downloads server
Please refer to our
mailing list archives
This track was produced at UCSC from data generated by scientists worldwide and curated by the
NCBI RefSeq project.
BLAT - the BLAST-like
alignment tool. Genome Res. 2002 Apr;12(4):656-64.
PMID: 11932250; PMC: PMC187518
Pruitt KD, Brown GR, Hiatt SM, Thibaud-Nissen F, Astashyn A, Ermolaeva O, Farrell CM, Hart J,
Landrum MJ, McGarvey KM et al.
RefSeq: an update on mammalian reference sequences.
Nucleic Acids Res. 2014 Jan;42(Database issue):D756-63.
PMID: 24259432; PMC:
Pruitt KD, Tatusova T, Maglott DR.
NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D501-4.
PMID: 15608248; PMC: PMC539979