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Mutant Information

Mutant NameFN1135-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1135-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000014 (Panicle Weight) = Low (Between 25% and 74%)
  • TO:0000207 (Plant height) = Normal (Between 75% and 125%)
  • TO:0000445 (Seed Number) = Low (Between 25% and 74%)
  • TO:0000430 (Germination Rate) = Low (Between 25% and 75%)
  • TO:0000639 (Seed fertility) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Phenotype Changes
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Mapping
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Variant Information

Single base substitutions: 25
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr110954371G-AHETINTRON
SBSChr117464025C-AHETINTRON
SBSChr138558000G-THETSYNONYMOUS_CODING
SBSChr138558002G-AHETNON_SYNONYMOUS_CODINGLOC_Os01g66379
SBSChr1017265405T-GHETNON_SYNONYMOUS_CODINGLOC_Os10g32980
SBSChr1017883302T-GHETINTERGENIC
SBSChr106778900A-THETINTERGENIC
SBSChr1113799841T-CHETINTERGENIC
SBSChr1122630088C-AHOMOINTERGENIC
SBSChr1123816458G-AHOMOINTERGENIC
SBSChr119981774G-AHETINTRON
SBSChr123993644C-THETINTRON
SBSChr230653835C-AHOMOINTRON
SBSChr231455036G-AHOMOINTERGENIC
SBSChr33676302C-THETINTRON
SBSChr42009016C-THETNON_SYNONYMOUS_CODINGLOC_Os04g04290
SBSChr56417555C-THETINTERGENIC
SBSChr716719969G-AHOMOINTERGENIC
SBSChr716719970G-AHOMOINTERGENIC
SBSChr721930601G-AHETINTERGENIC
SBSChr77837106C-THETINTERGENIC
SBSChr819681060A-GHETINTERGENIC
SBSChr911657418T-AHOMOINTERGENIC
SBSChr911972150G-AHETINTERGENIC
SBSChr98233485C-THETINTERGENIC

Deletions: 29
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr121779535177956934
DeletionChr72508686250869711
DeletionChr7403011740301203LOC_Os07g07990
DeletionChr115673100567311111
DeletionChr12845984084598422
DeletionChr11991767199176732LOC_Os11g17740
DeletionChr6128139521281397220
DeletionChr101502700115072000450009
DeletionChr615630732156323241592LOC_Os06g27630
DeletionChr1016090738160907391
DeletionChr1117308907173089081
DeletionChr317541140175411411
DeletionChr118185617181856192
DeletionChr11901629619044907286115
DeletionChr719026030190260322
DeletionChr219858325198583261
DeletionChr120022648200226502
DeletionChr820836443208364452
DeletionChr1213140012182500051100076
DeletionChr823451578234515879LOC_Os08g37115
DeletionChr4241322762413228913
DeletionChr7253706862537071529
DeletionChr3255808162558082913
DeletionChr326689070266890788
DeletionChr627010691270106976
DeletionChr427753065277530661
DeletionChr428962794289627951
DeletionChr129365632293656375LOC_Os01g51120
DeletionChr2336730503367308131

Insertions: 7
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1123050004230500052
InsertionChr1220273258202732592
InsertionChr1223551114235511152
InsertionChr212353499123535024
InsertionChr418959179189591802
InsertionChr426251100262511001LOC_Os04g44320image
InsertionChr627095370270953701

Inversions: 4
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr101503031016265459
InversionChr71638824217687708LOC_Os07g30020
InversionChr71638840117687730LOC_Os07g30020
InversionChr137890259381563052

Translocations: 5
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr93712680Chr1218258152
TranslocationChr46944309Chr137473759
TranslocationChr46944318Chr137472724LOC_Os01g64590
TranslocationChr716718148Chr121760272LOC_Os01g38780
TranslocationChr717792809Chr1217605732