A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\wMcp.scs'.14

General Information
SymbolDmel\wMcp.scs'.14SpeciesD. melanogaster
NameFlyBase IDFBal0102333
Feature typealleleAssociated geneDmel\w
Allele class
Mutagenin vitro construct - regulatory fusion
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Description
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FB2013_03
FB2013_02
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hide Nature of the Allele
Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Construct: Contains the 2.8kb EcoRI Mcp fragment followed by the w enhancer upstream of the w+mC minigene followed by the scs'0.5 element. The proximal end of the Mcp fragment is closest to the w minigene.
Carried in construct
Cytology
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Statement
Reference
Eye colour: P{Mcp-w#14} flies have similar or darker eye colours compared to P{wRW+we}. Position effect variegation can sometimes be seen. Homozygotes do not generally have a darker eye colour than heterozygotes, and can sometimes be lighter in colour. Pairing-sensitive silencing the mini-w gene occurs in about 55% of transformant lines.
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hideSuppressed by
Statement
Reference
wMcp.13, wMcp.scs'.14 has eye color defective phenotype, suppressible by pho[+]/pho1
wMcp.13, wMcp.scs'.14 has eye color defective phenotype, suppressible by pho[+]/phocv
wMcp.13, wMcp.scs'.14 has eye color defective phenotype, suppressible by Sce[+]/Sce1
wMcp.13, wMcp.scs'.14 has eye color defective phenotype, suppressible by ScmET50/Scm[+]
wMcp.scs'.13, wMcp.scs'.14 has eye color defective phenotype, suppressible by Sce[+]/Sce1
wMcp.scs'.14 has eye color defective phenotype, suppressible by Pcl10/Pcl[+]
wMcp.scs'.14 has eye color defective phenotype, suppressible by Sce[+]/Sce1
wMcp.scs'.14 has eye color defective phenotype, suppressible by ScmET50/Scm[+]
hideNOT suppressed by
Statement
Reference
wMcp.13, wMcp.scs'.14 has eye color defective phenotype, non-suppressible by Asx[+]/Asx1
wMcp.13, wMcp.scs'.14 has eye color defective phenotype, non-suppressible by Pc[+]/Pc2
wMcp.13, wMcp.scs'.14 has eye color defective phenotype, non-suppressible by Pcl10/Pcl[+]
wMcp.scs'.13, wMcp.scs'.14 has eye color defective phenotype, non-suppressible by Asx[+]/Asx1
wMcp.scs'.13, wMcp.scs'.14 has eye color defective phenotype, non-suppressible by Pc[+]/Pc2
wMcp.scs'.14 has eye color defective phenotype, non-suppressible by Asx1
wMcp.scs'.14 has eye color defective phenotype, non-suppressible by phocv/pho1
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hideSuppressed by
Statement
Reference
wMcp.13, wMcp.scs'.14 has pigment cell phenotype, suppressible by pho[+]/pho1
wMcp.13, wMcp.scs'.14 has pigment cell phenotype, suppressible by pho[+]/phocv
wMcp.13, wMcp.scs'.14 has pigment cell phenotype, suppressible by Sce[+]/Sce1
wMcp.13, wMcp.scs'.14 has pigment cell phenotype, suppressible by ScmET50/Scm[+]
wMcp.scs'.13, wMcp.scs'.14 has pigment cell phenotype, suppressible by Pcl10/Pcl[+]
wMcp.scs'.13, wMcp.scs'.14 has pigment cell phenotype, suppressible by Sce[+]/Sce1
wMcp.scs'.13, wMcp.scs'.14 has pigment cell phenotype, suppressible by ScmET50/Scm[+]
wMcp.scs'.14 has pigment cell phenotype, suppressible by Pcl10/Pcl[+]
wMcp.scs'.14 has pigment cell phenotype, suppressible by Sce[+]/Sce1
wMcp.scs'.14 has pigment cell phenotype, suppressible by ScmET50/Scm[+]
hideNOT suppressed by
Statement
Reference
wMcp.13, wMcp.scs'.14 has pigment cell phenotype, non-suppressible by Asx[+]/Asx1
wMcp.13, wMcp.scs'.14 has pigment cell phenotype, non-suppressible by Pc[+]/Pc2
wMcp.13, wMcp.scs'.14 has pigment cell phenotype, non-suppressible by Pcl10/Pcl[+]
wMcp.scs'.13, wMcp.scs'.14 has pigment cell phenotype, non-suppressible by Asx[+]/Asx1
wMcp.scs'.13, wMcp.scs'.14 has pigment cell phenotype, non-suppressible by Pc[+]/Pc2
wMcp.scs'.14 has pigment cell phenotype, non-suppressible by Asx1
wMcp.scs'.14 has pigment cell phenotype, non-suppressible by phocv/pho1
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Statement
Reference
The Pairing sensitive silencing effect seen in this allele is suppressed by heterozygous Sce1, strongly suppressed by ScmET50 or Pcl10 and is unaffected by heterozygous Asx1 or pho1/phocv. The Pairing sensitive silencing effect seen in wMcp.scs'.14/wMcp.13 (P{Mcp-w#14}AP-2stummelbein/+, P{Mcp-w#13}116/+) double insertions is suppressed by heterozygous Pcl10, strongly suppressed by heterozygous ScmET50, Sce1 and pho1/phocv, and is unaffected by heterozygous Asx1 and Pc2.
The Pairing sensitive silencing effect seen in this allele is suppressed by heterozygous Sce1, strongly suppressed by ScmET50 or Pcl10 and is unaffected by heterozygous Asx1 or pho1/phocv. The Pairing sensitive silencing effect seen in wMcp.scs'.14/wMcp.scs'.13 (P{Mcp-w#14}AP-2stummelbein/+, P{Mcp-w#13}116/+) double insertions is suppressed by heterozygous Pcl10, strongly suppressed by heterozygous ScmET50, Sce1 and pho1/phocv, and is unaffected by heterozygous Asx1 and Pc2.
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Statement
Reference
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Comments
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Discoverer
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Other Crossreferences
Linkouts
hide Synonyms & Secondary IDs ( 1 )
Reported As
Symbol Synonym
wMcp.scs'.14
 
Name Synonym
Secondary FlyBase IDs
hide References ( 2 )
Research paper
Shanower et al., 2005, Genetics 169(1): 173--184
Characterization of the grappa gene, the Drosophila histone H3 lysine 79 methyltransferase. [FBrf0183454]
Muller et al., 1999, Genetics 153(3): 1333--1356
The mcp element from the Drosophila melanogaster bithorax complex mediates long-distance regulatory interactions. [FBrf0111986]