A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\spid13

General Information
SymbolDmel\spid13SpeciesD. melanogaster
NameFlyBase IDFBal0028565
Feature typealleleAssociated geneDmel\spi
Allele class
MutagenX ray
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Description
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FB2013_03
FB2013_02
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Allele class
Mutagen
Mutations Mapped to the Genome
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Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
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UniProtKB/Swiss-Prot
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Progenitor genotype
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Caused by aberration
Cytology
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Statement
Reference
Epidermal defects and fusion of the anterior and posterior commissures. In the PNS some sensory organs are missing, there is a ventral-dorsal gradient of severity. Several muscle fibres are always missing in the dorsolateral region and there are variable abnormalities in the number, shape and attachment sites of the eight ventral oblique muscle fibres.
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hide Synonyms & Secondary IDs ( 2 )
Reported As
Symbol Synonym
spid13
 
Name Synonym
Secondary FlyBase IDs
hide References ( 5 )
Research paper
Rutledge et al., 1992, Genes Dev. 6: 1503--1517
The Drosophila spitz gene encodes a putative EGF-like growth factor involved in dorsal-ventral axis formation and neurogenesis. [FBrf0056107]
St. Johnston et al., 1990, Genes Dev. 4: 1114--1127
Molecular organization of the decapentaplegic gene in Drosophila melanogaster. [FBrf0051824]
Irish and Gelbart, 1987, Genes Dev. 1: 868--879
The decapentaplegic gene is required for dorsal-ventral patterning of the Drosophila embryo. [FBrf0046290]
Spencer et al., 1982, Cell 28(3): 451--461
Decapentaplegic: A gene complex affecting morphogenesis in Drosophila melanogaster. [FBrf0037609]
Book
Lindsley and Zimm, 1992, The Genome of Drosophila melanogaster.
The Genome of Drosophila melanogaster. [FBrf0066905]