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Schema for HInvGeneMrna
  Database: hg16    Primary Table: HInvGeneMrna    Row Count: 44,560   Data last updated: 2004-06-28
Format description: Summary info about a patSpace alignment
On download server: MariaDB table dump directory
fieldexampleSQL type info description
bin 585smallint(5) unsigned range Indexing field to speed chromosome range queries.
matches 1973int(10) unsigned range Number of bases that match that aren't repeats
misMatches 21int(10) unsigned range Number of bases that don't match
repMatches 0int(10) unsigned range Number of bases that match but are part of repeats
nCount 0int(10) unsigned range Number of 'N' bases
qNumInsert 2int(10) unsigned range Number of inserts in query
qBaseInsert 3int(10) unsigned range Number of bases inserted in query
tNumInsert 9int(10) unsigned range Number of inserts in target
tBaseInsert 12990int(10) unsigned range Number of bases inserted in target
strand -char(2) values + or - for strand. First character query, second target (optional)
qName HIT000020038varchar(255) values Query sequence name
qSize 1997int(10) unsigned range Query sequence size
qStart 0int(10) unsigned range Alignment start position in query
qEnd 1997int(10) unsigned range Alignment end position in query
tName chr1varchar(255) values Target sequence name
tSize 246127941int(10) unsigned range Target sequence size
tStart 4222int(10) unsigned range Alignment start position in target
tEnd 19206int(10) unsigned range Alignment end position in target
blockCount 12int(10) unsigned range Number of blocks in alignment
blockSizes 470,69,108,44,162,199,260,2...longblob   Size of each block
qStarts 0,470,539,648,692,854,1053,...longblob   Start of each block in query.
tStarts 4222,4832,5658,5766,6469,67...longblob   Start of each block in target.

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
        hg16.HInv.geneId (via HInvGeneMrna.qName)
      hg16.knownToHInv.value (via HInvGeneMrna.qName)

Sample Rows
 
binmatchesmisMatchesrepMatchesnCountqNumInsertqBaseInserttNumInserttBaseInsertstrandqNameqSizeqStartqEndtNametSizetStarttEndblockCountblockSizesqStartstStarts
5851973210023912990-HIT000020038199701997chr124612794142221920612470,69,108,44,162,199,260,259,147,99,154,23,0,470,539,648,692,854,1053,1315,1574,1721,1820,1974,4222,4832,5658,5766,6469,6719,7095,7355,7777,8130,14600,19183,
58534474100411911592-HIT000026002353603499chr124612794142661934614108,316,271,303,360,198,661,198,260,250,147,99,154,163,37,145,461,738,1043,1404,1602,2263,2461,2723,2973,3120,3219,3373,4266,4376,4832,5103,5406,5766,5967,6720,7095,7355,7777,8130,14600,19183,
5854213210012293-HIT000007755423604236chr12461279414269859631499,859,1876,0,1501,2360,4269,5769,6720,
5853135190027711784-HIT000017450316103161chr1246127941426919207953,1446,859,198,136,137,147,154,24,0,58,1506,2365,2563,2699,2836,2983,3137,4269,4322,5769,6720,7095,7468,7777,14600,19183,
5851659210022741013259-HIT000014558195401954chr124612794142691920812423,69,108,44,162,199,136,140,121,99,154,25,0,423,492,601,645,807,1006,1142,1555,1676,1775,1929,4269,4832,5658,5766,6469,6719,7095,7468,7803,8130,14600,19183,
58523341300271213247-HIT000012846235402354chr12461279414269198631449,374,69,110,41,162,199,136,137,147,99,154,582,88,0,54,428,497,609,650,812,1011,1147,1284,1431,1530,1684,2266,4269,4318,4832,5658,5769,6469,6719,7095,7468,7777,8130,14600,19183,19775,
5852802000026577-HIT0000145581954391673chr1246127941789814757326,99,157,1281,1307,1406,7898,8130,14600,
585438121000014429-HIT000007722440404402chr1246127941103691920024385,17,2,4387,10369,19183,
5851860270000315-HIT000012176188901887chr124612794193495953974528,146,1165,48,2,530,676,1841,93495,94025,94183,95349,
5852340710033499-HIT000021935242062420chr124612794112463612714681798,76,45,97,161,184,43,7,0,1798,1874,1920,2017,2178,2363,2407,124636,126483,126560,126605,126703,126912,127096,127139,

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

H-Inv (HInvGeneMrna) Track Description
 

Description

This track shows alignments of full-length cDNAs that were used as the basis of the H-Invitational Gene Database (HInv-DB). The HInv-DB is a human gene database containing human-curated annotation of 41,118 full-length cDNA clones representing 21,037 cDNA clusters. The project was initiated in 2002 and the database became publicly available in April 2004.

HInv-DB entries describe the following entities:

  • gene structures
  • functions
  • novel alternative splicing isoforms
  • non-coding functional RNAs
  • functional domains
  • sub-cellular localizations
  • metabolic pathways
  • predictions of protein 3D structure
  • mapping of SNPs and microsatellite repeat motifs in relation with orphan diseases
  • gene expression profiling
  • comparative results with mouse full-length cDNAs gene structures

Methods

To cluster redundant cDNAs and alternative splicing variants within the H-Inv cDNAs, a total of 41,118 H-Inv cDNAs were mapped to the human genome using the mapping pipeline developed by the Japan Biological Information Research Center (JBIRC). The mapping yielded 40,140 cDNAs that were aligned against the genome using the stringent criteria of at least 95% identity and 90% length coverage. These 40,140 cDNAs were clustered to 20,190 loci, resulting in an average of 2.0 cDNAs per locus. For the remaining 978 unmapped cDNAs, cDNA-based clustering was applied, yielding 847 clusters. In total, 21,037 clusters (20,190 mapped and 847 unmapped) were identified and integrated into H-InvDB. H-Inv cluster IDs (e.g. HIX0000001) were assigned to these clusters. A representative sequence was selected from each cluster and used for further analyses and annotation.

A full description of the construction of the HInv-DB is contained in the report by the H-Inv Consortium (see References section).

Credits

The H-InvDB is hosted at the JBIRC. The human-curated annotations were produced during invitational annotation meetings held in Japan during the summer of 2002, with a follow-up meeting in November 2004. Participants included 158 scientists representing 67 institutions from 12 countries.

The full-length cDNA clones and sequences were produced by the Chinese National Human Genome Center (CHGC), the Deutsches Krebsforschungszentrum (DKFZ/MIPS), Helix Research Institute, Inc. (HRI), the Institute of Medical Science in the University of Tokyo (IMSUT), the Kazusa DNA Research Institute (KDRI), the Mammalian Gene Collection (MGC/NIH) and the Full-Length Long Japan (FLJ) project.

References

Imanishi T, Itoh T, Suzuki Y, O'Donovan C, Fukuchi S, Koyanagi KO, Barrero RA, Tamura T, Yamaguchi- Kabata Y, Tanino M et al. Integrative annotation of 21,037 human genes validated by full-length cDNA clones. PLoS Biol. 2004 Jun;2(6):e162. PMID: 15103394; PMC: PMC393292