FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\srpneo45
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General Information
Symbol
Dmel\srpneo45
Species
D. melanogaster
Name
FlyBase ID
FBal0011058
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
srpAS, srpp282
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P{hsneo} insertion within 5' flanking sequences.

Mutations Mapped to the Genome
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

In srpneo45 embryos, the lymph gland does not form but most cardioblasts and pericardial cells do form.

srp3/srpneo45 embryos lack all hemocytes yet show an entirely normal time course of wound reepithelialization.

The average number of crystal cells per embryo is reduced in homozygous stage 13-14 embryos compared to wild type.

Mutant embryos lack macrophages and have defects in the central nervous system axon scaffold (which has a rounded appearance). Increased numbers of repo-positive glial cells are present at the midline compared to wild type, while the glia associated with the longitudinal tracts appear more dispersed than in wild type.

Mutants embryos lack blood cells. During stages 11-13 have some missing tracheal cells. Also a small group of cells near each tracheal visceral branch, and a small group ventral midline cells in each segment, possibly midline glia.

Mutants lack hemocytes.

Homozygous embryos exhibit weak germ band retraction defects, one or no ventral setae remain on the dorsal aspect of the embryo. Kr staining reveals abnormalities in the amnioserosa.

Semi-viable.

Homozygous embryos exhibit severe reduction in number of mature haemocytes and srp2/srpneo45 and srp3/srpneo45 transheterozygous embryos are devoid of any mature haemocytes.

The fat body appears normal in mutant embryos. Hemocytes are missing.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhanced by
Statement
Reference

srpneo45 has phenotype, enhanceable by ush2

Enhancer of
Statement
Reference

srpneo45 is an enhancer of phenotype of ush2

srpneo45 is an enhancer of phenotype of pebhnt-1

Suppressor of
Statement
Reference

srpneo45/srp[+] is a suppressor of lamellocyte | larval stage phenotype of ushVX22

srpneo45/srp[+] is a suppressor of hemocyte | larval stage phenotype of ushVX22

Additional Comments
Genetic Interactions
Statement
Reference

Lamellocyte production is drastically reduced in ushVX22/+, srpneo45/+ double heterozygous mutant larvae, but not quite to wild-type levels. The number of non-lamellocyte cells is reduced to almost half the wild-type value.

Germ band retraction defects are more severe than the single homozygote when in combination with ush2 or pebhnt-1.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

A. Spradling.

Cooley et al.

Comments
Comments

Complements: tara03881. Complements: Akt104226. Complements: l(3)0520305203. Complements: l(3)0872408724.

P{hsneo} insertion specifically affects the srp function required for development of the haemocytes, probably a regulatory region which is essential for the anterior mesodermal srp expression.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (11)
References (25)