A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\ea161.13

General Information
SymbolDmel\ea161.13SpeciesD. melanogaster
NameFlyBase IDFBal0031156
Feature typealleleAssociated geneDmel\ea
Map ( GBrowse ) GBrowse View Helpdetailed view FBal0003481 FBal0003466 FBal0003477 FBal0003468 FBal0003482 FBal0003476 FBal0003479 FBal0003480 FBal0003455 FBal0003474 FBal0003462 FBal0031156 FBal0003483
Allele classgain of function allele
Mutagenethyl methanesulfonate
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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
Type
Location
Additional Notes
References
point mutation
evidence=experimental
na_change=G11156015A
pr_change=G371R|ea-PA
reported_na_change=G5564A
reported_pr_change=G371R
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Nucleotide substitution: G1314A.
Amino acid replacement: G371R.
Cytology
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Statement
Reference
62% of embryos derived from ea161.13/+ females crossed to wild-type males die. 100% of the dead embryos are very weakly ventralised (head involution does not occur and some embryos have a tail up phenotype, Filzkorper are normal).
62% embryos from heterozygous females crossed to wild type males die and are weakly ventralised. Embryos show failure of head involution and 25% have a 'tail-up' phenotype due to an incomplete retraction of the germ band.
Weakly ventralised embryos. When maternal or zygotic tkv levels are reduced most of the embryos die and show an increased level of ventralisation.
Embryos weakly ventralized.
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Statement
Reference
ea161.13 has phenotype, enhanceable by put135
ea161.13 has phenotype, enhanceable by shn1
ea161.13 has phenotype, enhanceable by vri1
ea161.13 has phenotype, enhanceable by vri2
ea161.13 has phenotype, enhanceable by vri5R4.11
ea161.13 has phenotype, enhanceable by vri5R5.7
ea161.13 has phenotype, enhanceable by vri5R5.24
ea161.13 has phenotype, enhanceable by vri5R7.2
ea161.13 has phenotype, enhanceable by vri5R8.4
ea161.13 has phenotype, enhanceable by vrik03801
ea161.13 has phenotype, enhanceable by vrik05901
ea161.13 has phenotype, enhanceable by vrik09602
ea161.13 has phenotype, enhanceable by vrik09713
ea161.13 has phenotype, enhanceable by vrik11805
ea161.13 has stage 14 embryo phenotype, enhanceable by cype[+]/cype03771
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Statement
Reference
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Statement
Reference
99% of embryos derived from cype03771/+ ; ea161.13/+ females crossed to wild-type males die with a ventralised phenotype. 10% are very weakly ventralised (head involution does not occur and some embryos have a tail up phenotype, Filzkorper are normal), 80% are weakly ventralised (the head is not involuted, the posterior segments are internalised and the Filzkorper are disorganised) and 10% are moderately ventralised (the ventral denticle belt is extended laterally, Filzkorper are reduced and disorganised, the head is not involuted and the head and thorax are extended and convoluted).
When in combination with vrik05901, vrik09713, vri5R5.7, vri5R5.7 and vri5R5.7 all embryos die. When in combination with other vri alleles, Df(2L)tkv2, shn1 and put135 lethality is greatly increased and embryos are more strongly ventralised.
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Reference
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Comments
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Discoverer
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hide Synonyms & Secondary IDs ( 1 )
Reported As
Symbol Synonym
Name Synonym
Secondary FlyBase IDs
hide References ( 4 )
Research paper
Szuplewski and Terracol, 2001, Genetics 158(4): 1629--1643
The cyclope gene of Drosophila encodes a cytochrome c oxidase subunit VIc homolog. [FBrf0138407]
George and Terracol, 1997, Genetics 146(4): 1345--1363
The vrille gene of Drosophila is a maternal enhancer of decapentaplegic and encodes a new member of the bZIP family of transcription factors. [FBrf0094777]
Terracol and Lengyel, 1994, Genetics 138(1): 165--178
The thick veins gene of Drosophila is required for dorsoventral polarity of the embryo. [FBrf0076541]
Jin and Anderson, 1990, Cell 60: 873--881
Dominant and recessive alleles of the Drosophila easter gene are point mutations at conserved sites in the serine protease catalytic domain. [FBrf0051391]