A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Gene Dmel\qs

General Information
SymbolDmel\qsSpeciesD. melanogaster
NamequicksilverAnnotation symbol
Feature typegeneFlyBase IDFBgn0003186
Gene Model StatusUnannotated Stock availability 5 publicly available
Also Known Asftd
Genomic Location
Chromosome (arm)Recombination map1-39.5
Cytogenetic map10F1-10F7Sequence location
hide Summary Information
Automatically generated summary

See sections below for more information
The gene quicksilver is referred to in FlyBase by the symbol Dmel\qs (FBgn0003186). It is a gene from Drosophila melanogaster. Its molecular function is unknown. The biological processes in which it is involved are not known. 12 alleles are reported. The phenotypes of these alleles are annotated with: cephalopharyngeal skeleton; cuticle; puparium; denticle belt. It has no annotated transcripts. Gene has not been localized to the genome sequence.

User Contributed Data
hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
qs: quicksilver
Recessive embryonic lethal; denticles and mouthparts unpigmented; cell viable in gynandromorphs causing depigmentation of cuticle, including chaetae; viability reduced owing to weakened cuticle. Used as marker in the analysis of mosaic embryos (Gergen and Wieschaus, 1985, Dev. Biol. 109: 321-35). qs1, qs2, and qs3 hypomorphic in that expression varies with temperature and nutrition; some survival when reared on enriched medium; survivors smaller than normal and incompletely pigmented with a yellowish tinge; some extremely pale with bristles with very little pigmentation and with wings that when expanded are glassy clear and very fragile. The extremely pale qs2/Y never exhibit melanotic wound reaction, and puparia underpigmented. qs embryos derived from homozygous germ-line clones do not hatch and exhibit head defects and abnormalities of germ-band shortening; heterozygous embryos from such clones exhibit 75% survival; homozygous clones behave as meiotic mutant yielding 8% patroclinous males (Wieschaus and Noel, 1986, Wilhelm Roux's Arch. Dev. Biol. 195: 63-73). Phenol oxidase activity of any surviving qs flies significantly depressed, in some cases being undetectable; all three components, A1, A2, and A3, coordinately reduced; activator activity normal. Phenol oxidase deficiency leads to significant accumulations of catecholamine pools in qs2 males 60 to 80 min after eclosion: three-to-eight-fold increases in N-β-alanyldopamine and N-acetyldopamine and two-fold increases in dopamine (Pentz, Black, and Wright).
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FB2013_03
FB2013_02
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hide Detailed Mapping Data
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
10F1-10F7  
Left limit from inclusion within Df(1)RA47 (FBrf0040717) Right limit from inclusion within Df(1)HA85 (FBrf0040178)  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
Experimentally Determined Recombination Data
Location
1-39.5
 
Left of (cM)
Right of (cM)
Notes
Mapping based on qs2.
 
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Comments on Gene Model
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Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Associated CDS (aa)
Additional Transcript Data & Comments
Reported size (kB)
Comments
External Data
Crossreferences
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Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
Additional Polypeptide Data & Comments
Reported size (kDa)
Comments
External Data
Linkouts
Crossreferences
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DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
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Type
Symbol & Location
Additional Notes
References
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Linkouts
Crossreferences
hide Expression Data
hideTranscript Expression
Additional Descriptive Data
Marker for
Subcellular Localization
CV Term
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Additional Descriptive Data
Marker for
Subcellular Localization (GO Cellular Component)
CV term
References
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Associated Tools
Reference
See Gelbart and Emmert, 2010.10.13 for analysis details and data files for all genes.
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Linkouts
hide Alleles & Phenotypes
hide Summary of Allele Phenotypes
Lethality
Allele
Phenotype manifest in
Allele
hide Classical Alleles ( 12 )
For All Classical Alleles Show

Allele of qsClassMutagenStocksKnown lesion
qs12 Yes
qs22 --
qs81 --
qs30 Yes
qs40 --
qs50 --
qs60 --
qs70 --
qs90 --
qsEH4970 --
qsftd-IV80 --
qsunspecified
0 --
hide Alleles Carried on Transgenic Constructs ( 0 )
For All Alleles Carried on Transgenic Constructs Show

Allele of qsClassMutagenStocksKnown lesion
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Disrupted in
Duplicated in
Not disrupted in
Not duplicated in
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Transgenic Constructs
Type of construct
Name
Expression data
Insertions
Type of insertions
Name
Expression data
hide Gene Ontology: Function, Process & Cellular Component ( 0 unique terms )
hide Terms Based on Experimental Evidence ( 0 terms )
hide Terms Based on Predictions or Assertions ( 0 terms )
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hide Summary of Physical Interactions
hide Summary of Genetic Interactions
Interacts with
Please look at the allele data for full details of the genetic interactions
qs allele
Gene
References
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Linkouts
DroID - A comprehensive database of gene and protein interactions.
hide Orthologs
hide OrthoDB Orthologs (0) - based on analysis using Dmel annotation version 5.41
OrthoDB Ortholog Groups
Drosophila inclusive ortholog search
No orthologs identified
Dipteran inclusive ortholog search
No orthologs identified
Insect inclusive ortholog search
No orthologs identified
Arthropod inclusive ortholog search
No orthologs identified
Metazoa inclusive ortholog search
No orthologs identified
Orthologs in Drosophila Species (None identified)
No orthologies identified
Orthologs in non-Drosophila Dipterans (None identified)
No non-Drosophilid orthologies identified
Orthologs in non-Dipteran Insects (None identified)
No non-Dipteran orthologies identified
Orthologs in non-Insect Arthropods (None identified)
No non-Insect Arthropod orthologies identified
Orthologs in non-Arthropod Metazoa (None identified)
No non-Arthropod Metazoa orthologies identified
hide Human Orthologs (0)
Gene
OMIM
HGNC
hideAAA Orthologs (0) based on analysis using Dmel annotation version 4.3
No orthologs identified
hide Stocks & Reagents
hide Stocks Listed in FlyBase ( 5 )
Bloomington
Kyoto
107698
hide Genomic Clones ( 0 )
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cDNA Clones, Fully Sequenced
BDGP DGC clones
Other clones
cDNA Clones, End Sequenced (ESTs)
BDGP DGC clones
Other clones
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Linkouts
GenomeRNAi - GenomeRNAi – A database for cell-based and in vivo RNAi phenotypes and reagents
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Source for database identity of
Source for database merge of
Additional comments
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A screen for X-linked genes that affect embryo morphology revealed qs.
qs mutants display unpigmented larvae.
Recessive embryonic lethal; denticles and mouthparts unpigmented; cell viable in gynandromorphs causing depigmentation of cuticle, including chaetae; viability reduced owing to weakened cuticle. Used as marker in the analysis of mosaic embryos (Gergen and Wieschaus, 1985). qs1, qs2, and qs3 hypomorphic in that expression varies with temperature and nutrition; some survival when reared on enriched medium; survivors smaller than normal and incompletely pigmented with a yellowish tinge; some extremely pale with bristles with very little pigmentation and with wings that when expanded are glassy clear and very fragile. The extremely pale qs2/Y never exhibit melanotic wound reaction and puparia underpigmented. qs embryos derived from homozygous germ-line clones do not hatch and exhibit head defects and abnormalities of germ-band shortening; heterozygous embryos from such clones exhibit 75% survival; homozygous clones behave as meiotic mutant yielding 8% patroclinous males (Wieschaus and Noell, 1986). Phenol oxidase activity of any surviving qs flies significantly depressed, in some cases being undetectable; all three components, A1, A2 and A3, coordinately reduced; activator activity normal. Phenol oxidase deficiency leads to significant accumulations of catecholamine pools in qs2 males 60 to 80 min after eclosion: three-to-eight-fold increases in N-β-alanyldopamine and N-acetyldopamine and two-fold increases in dopamine (Pentz, Black and Wright, 1990).
 
hide External Crossreferences & Linkouts
Sequence Crossreferences
Other Crossreferences
Linkouts
DroID - A comprehensive database of gene and protein interactions.
GenomeRNAi - GenomeRNAi – A database for cell-based and in vivo RNAi phenotypes and reagents
hide Synonyms & Secondary IDs ( 7 )
Reported As
Symbol Synonym
l(1)10Fl
 
Name Synonym
faintoid
 
quicksilver
Secondary FlyBase IDs
hide References ( 20 )
Research paper
Cook et al., 2010, Genetics 186(4): 1095--1109
A new resource for characterizing X-linked genes in Drosophila melanogaster: systematic coverage and subdivision of the X chromosome with nested, Y-linked duplications. [FBrf0212582]
Anaka et al., 2008, J. Neurogenet. 22(4): 243--276
The white gene of Drosophila melanogaster encodes a protein with a role in courtship behavior. [FBrf0207087]
Lammel and Saumweber, 2000, Dev. Genes Evol. 210(11): 525--535
X-linked loci of Drosophila melanogaster causing defects in the morphology of the embryonic salivary glands. [FBrf0134551]
Harbecke and Lengyel, 1995, Rouxs Arch. Dev. Biol. 204(5): 308--329
Genes controlling posterior gut development in the Drosophila embryo. [FBrf0082073]
Pentz et al., 1990, Biochem. Genet. 28(3/4): 151--171
Mutations affecting phenol oxidase activity in Drosophila: quicksilver and tyrosinase-1. [FBrf0051216]
Eberl and Hilliker, 1988, Genetics 118: 109--120
Characterization of X-linked recessive lethal mutations affecting embryonic morphogenesis in Drosophila melanogaster. [FBrf0048191]
Alexandrov and Alexandrova, 1986, D. I. S. 63: 159--161
Report of new mutants. [FBrf0044054]
Wieschaus and Noell, 1986, Rouxs Arch. Dev. Biol. 195(1): 63--73
Specificity of embryonic lethal mutations in Drosophila analyzed in germ line clones. [FBrf0045374]
Gergen and Wieschaus, 1985, Dev. Biol. 109: 321--335
The localized requirements for a gene affecting segmentation in Drosophila: Analysis of larvae mosaic for runt. [FBrf0042365]
Craymer, 1984, D. I. S. 60: 234--236
[New mutants report.] [FBrf0063387]
Wieschaus et al., 1984, Rouxs Arch. Dev. Biol. 193: 296--307
Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster. [FBrf0040178]
Wieschaus et al., 1984, Dev. Biol. 104: 172--186
Kruppel, a gene whose activity is required early in the zygotic genome for normal embryonic segmentation. [FBrf0040717]
Sherald, 1981, Mol. Gen. Genet. 183: 102--106
Intergenic suppression of the black mutation of Drosophila melanogaster. [FBrf0037053]
Review
Martinez Arias, 1993, Bate, Martinez Arias, 1993: 517--608
Development and patterning of the larval epidermis of Drosophila. [FBrf0064786]
Wright, 1987, Adv. Genet. 24: 127--222
The genetics of biogenic amine metabolism, sclerotization, and melanization in Drosophila melanogaster. [FBrf0045547]
Personal communication to FlyBase
Gornek et al., 2000.2.4, Dp(1;Y)s for the 10C to 11D Region.
Dp(1;Y)s for the 10C to 11D Region. [FBrf0125111]
Abstract
Peyre and Aigaki, 2001, A. Dros. Res. Conf. 42: 59
Molecular and genetic analyses of Sex-Peptide action in Drosophila melanogaster. [FBrf0133666]
Stock list
The Moscow Regional Drosophila melanogaster Stock Center, Dubna, Russia, 1997, D. I. S. 80: 109--130
Stock list. [FBrf0098381]
Tearle and Nusslein-Volhard, 1987, D. I. S. 66: 209--269
Tubingen mutants and stock list. [FBrf0045941]
Book
Lindsley and Zimm, 1992, The Genome of Drosophila melanogaster.
The Genome of Drosophila melanogaster. [FBrf0066905]