FB2024_03 , released June 25, 2024
Allele: Dmel\timblind
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General Information
Symbol
Dmel\timblind
Species
D. melanogaster
Name
blind
FlyBase ID
FBal0177468
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: A1128V. Amino acid replacement: L1131M.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Nucleotide change:

C3500027T

Amino acid change:

A1105V | tim-PB; A1104V | tim-PL; A1105V | tim-PM; A1105V | tim-PP; A1073V | tim-PR; A1073V | tim-PS; A1128V | tim-PT; A1105V | tim-PU

Reported amino acid change:

A1128V

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two mutations in this line. The difference in the reported and annotated positions of the mutations is due to the use of a downstream translation start (23aa) in the current tim gene annotations.

Nucleotide change:

C3500019A

Amino acid change:

L1108M | tim-PB; L1107M | tim-PL; L1108M | tim-PM; L1108M | tim-PP; L1076M | tim-PR; L1076M | tim-PS; L1131M | tim-PT; L1108M | tim-PU

Reported amino acid change:

L1131M

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two mutations in this line. The difference in the reported and annotated positions of the mutations is due to the use of a downstream translation start (23aa) in the current tim gene annotations.

Variant Molecular Consequences
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

Under LD conditions, mutant adults behave similarly to wild-type flies in locomotor rhythm assays. The free-running locomotor activity period of homozygous males is 26 hours, 2 hours longer than that of controls. Heterozygous mutants also show a mild lengthening of the locomotor rhythm period under free-running conditions. The free-running eclosion period of mutant animals is the normal 24 hours. Analysis of the phase response curve (PRC) of timblind flies to brief pulses of light indicates that they react with small (1.5 hour) phase delays to light pulses given at ZT15 and ZT17, which normally causes delays of about 3 hours. When the light pulse is given at ZT19, the timblind flies react with a 1 hour phase delay, in contrast to wild-type flies, which react with a 3.5 hour phase advance. At ZT21, the mutant flies show robust phase advances, whereas controls already show a reduction in the amount of phase advances at this time. Overall, the timblind PRC is blunted in the delay portion, and the transition point (where delay changes to advance) is retarded by about 2 hours.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT Enhanced by
Statement
Reference

timblind has abnormal locomotor rhythm phenotype, non-enhanceable by sgg[+]/sgg32

NOT suppressed by
Statement
Reference

timblind has abnormal locomotor rhythm phenotype, non-suppressible by sgg[+]/sgg32

Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

More than 80% of adults expressing sggEP1576 under the control of Scer\GAL4tim.PE in a timblind background rapidly become arrhythmic for locomotor activity after they are placed in constant darkness conditions. The few animals that are rhythmic have a locomotor activity period that is intermediate between that of timblind homozygotes and that of adults expressing sggEP1576 under the control of Scer\GAL4tim.PE in a wild-type background. The increase in locomotor rhythm period length seen in timblind homozygous flies in free-running conditions is not further increased if the flies also carry sgg32.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (2)