Schema for xenoRefGene
  Database: taeGut1    Primary Table: xenoRefGene    Row Count: 232,365   Data last updated: 2020-09-01
Format description: A gene prediction with some additional info.
On download server: MariaDB table dump directory
fieldexampleSQL type info description
bin 637smallint(5) unsigned range Indexing field to speed chromosome range queries.
name NM_001172417varchar(255) values Name of gene (usually transcript_id from GTF)
chrom chr9varchar(255) values Reference sequence chromosome or scaffold
strand -char(1) values + or - for strand
txStart 6926568int(10) unsigned range Transcription start position (or end position for minus strand item)
txEnd 6928292int(10) unsigned range Transcription end position (or start position for minus strand item)
cdsStart 6926568int(10) unsigned range Coding region start (or end position for minus strand item)
cdsEnd 6928268int(10) unsigned range Coding region end (or start position for minus strand item)
exonCount 2int(10) unsigned range Number of exons
exonStarts 6926568,6928048,longblob   Exon start positions (or end positions for minus strand item)
exonEnds 6927191,6928292,longblob   Exon end positions (or start positions for minus strand item)
score 0int(11) range score
name2 KCNJ13varchar(255) values Alternate name (e.g. gene_id from GTF)
cdsStartStat cmplenum('none', 'unk', 'incmpl', 'cmpl') values Status of CDS start annotation (none, unknown, incomplete, or complete)
cdsEndStat cmplenum('none', 'unk', 'incmpl', 'cmpl') values Status of CDS end annotation (none, unknown, incomplete, or complete)
exonFrames 1,0,longblob   Reading frame of the start of the CDS region of the exon, in the direction of transcription (0,1,2), or -1 if there is no CDS region.

To download this table in different text formats or to intersect or correlate it with other tables, use the Table Browser.

Connected Tables and Joining Fields
        hgFixed.gbCdnaInfo.acc (via xenoRefGene.name)
      hgFixed.gbMiscDiff.acc (via xenoRefGene.name)
      hgFixed.gbSeq.acc (via xenoRefGene.name)
      hgFixed.gbWarn.acc (via xenoRefGene.name)
      hgFixed.imageClone.acc (via xenoRefGene.name)
      taeGut1.all_est.qName (via xenoRefGene.name)
      taeGut1.all_mrna.qName (via xenoRefGene.name)
      taeGut1.refGene.name (via xenoRefGene.name)
      taeGut1.refSeqAli.qName (via xenoRefGene.name)
      taeGut1.xenoMrna.qName (via xenoRefGene.name)
      taeGut1.xenoRefFlat.name (via xenoRefGene.name)
      taeGut1.xenoRefSeqAli.qName (via xenoRefGene.name)

Sample Rows
 
binnamechromstrandtxStarttxEndcdsStartcdsEndexonCountexonStartsexonEndsscorename2cdsStartStatcdsEndStatexonFrames
637NM_001172417chr9-692656869282926926568692826826926568,6928048,6927191,6928292,0KCNJ13cmplcmpl1,0,
637NM_001172416chr9-692656869284036927130692840326926568,6928284,6927191,6928403,0KCNJ13incmplcmpl2,0,
1723NM_001024174chrUn+1491718751491729911491718751491729915149171875,149172007,149172196,149172775,149172910,149171983,149172034,149172478,149172910,149172991,0pcdh2g1incmplincmpl0,0,0,0,0,
167NM_001109152chr1+991981779926070699198177992607061299198177,99230061,99233575,99234232,99240928,99243174,99246923,99248780,99251720,99253144,99255073,99260592,99198288,99230169,99233667,99234290,99241018,99243288,99246930,99248844,99251870,99253225,99255223,99260706,0Gdpd5incmplincmpl0,2,0,2,0,0,0,1,0,0,0,2,
937NM_001013757chr2-462380634625047246238063462504721346238063,46238236,46238338,46238476,46239577,46239802,46241998,46242414,46243319,46244548,46246053,46248763,46250292,46238185,46238317,46238449,46238581,46239700,46240079,46242069,46242627,46243442,46244636,46246215,46248994,46250472,0Vwdeincmplincmpl0,0,0,0,0,2,0,0,0,0,0,0,0,
634NM_146963chr5-642745964281276427459642812746427459,6427734,6427905,6428028,6427481,6427770,6428001,6428127,0Olfr45incmplincmpl0,0,0,0,
594NM_001077277chr25+1222656123526712226561235267171222656,1223756,1224141,1224184,1224356,1224742,1225301,1229447,1230291,1230439,1230615,1231686,1232099,1234073,1234202,1234643, ...1222838,1223838,1224184,1224331,1224359,1224869,1225345,1229902,1230408,1230441,1230783,1231817,1232135,1234124,1234283,1234732, ...0setdb1bincmplincmpl0,2,1,0,0,0,1,0,2,2,1,1,0,0,0,0,2,
82NM_001094539chr7+100924921009856610092492100985661110092492,10092932,10093047,10093690,10093884,10094060,10094260,10094545,10095120,10098265,10098497,10092603,10093001,10093050,10093795,10093914,10094129,10094422,10094671,10095240,10098415,10098566,0slc11a1.Lincmplincmpl0,0,0,0,0,0,0,0,0,0,0,
614NM_001171733chr28-390056339011003900563390110013900563,3901100,0tnfaip8l2.Scmplincmpl0,
585NM_001280587chr24+65903667646590366764365903,66495,66644,66116,66555,66764,0cxcr5.Lincmplincmpl0,1,0,

Note: all start coordinates in our database are 0-based, not 1-based. See explanation here.

Other RefSeq (xenoRefGene) Track Description
 

Description

This track shows known protein-coding and non-protein-coding genes for organisms other than mouse, taken from the NCBI RNA reference sequences collection (RefSeq). The data underlying this track are updated weekly.

Display Conventions and Configuration

This track follows the display conventions for gene prediction tracks. The color shading indicates the level of review the RefSeq record has undergone: predicted (light), provisional (medium), reviewed (dark).

The item labels and display colors of features within this track can be configured through the controls at the top of the track description page.

  • Label: By default, items are labeled by gene name. Click the appropriate Label option to display the accession name instead of the gene name, show both the gene and accession names, or turn off the label completely.
  • Codon coloring: This track contains 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. Click here for more information about this feature.
  • Hide non-coding genes: By default, both the protein-coding and non-protein-coding genes are displayed. If you wish to see only the coding genes, click this box.

Methods

The RNAs were aligned against the mouse genome using blat; those with an alignment of less than 15% were discarded. At least 40 bases must be aligned to DNA that is not repeat masked. 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 1.0% of the best and at least 35% base identity with the genomic sequence were kept.

Credits

This track was produced at UCSC from RNA sequence data generated by scientists worldwide and curated by the NCBI RefSeq project.

References

Kent WJ. BLAT--the BLAST-like alignment tool. Genome Res. 2002 Apr;12(4):656-64. PMID: 11932250; PMC: PMC187518