FlyBase Allele Report: Dmel\Atpα[CJ10]

General Information

Symbol

Dmel\Atpα^CJ10

Species

D. melanogaster

Name

FlyBase ID

FBal0282773

Feature type

allele

Associated gene

Dmel\Atpα

Associated Insertion(s)

Carried in Construct

Also Known As

ATPalpha^CJ10

Key Links

Genomic Maps

JBrowse

Allele class

Mutagen

ethyl methanesulfonate

Nature of the Allele

Allele class

Mutagen

ethyl methanesulfonate

(Ashmore et al., 2009)

Progenitor genotype

Cytology

Description

Amino acid replacement: G744S.

(Ashmore et al., 2009)

Nucleotide substitution: G?A.

(Ashmore et al., 2009)

Atpα protein expression levels are not significantly altered in heterozygotes.

(Ashmore et al., 2009)

Mutations Mapped to the Genome

Curation Data

Type

Location

Additional Notes

References

point_mutation

3R:20,966,458..20,966,458 [+]

Nucleotide change:

G20966458A

Reported nucleotide change:

G?A

Amino acid change:

Reported amino acid change:

G744S

(Ashmore et al., 2009)

Variant Molecular Consequences

Associated Sequence Data

DDBJ / EMBL / GenBank

DNA sequence

Protein sequence

UniProtKB/Swiss-Prot

UniProtKB/TrEMBL

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 ( 1 )

Disease

Evidence

References

model of familial hemiplegic migraine

CEA

(Ashmore et al., 2009)

model of nervous system disease

CEA

(Talsma et al., 2014)

Modifiers Based on Experimental Evidence ( 1 )

Disease

Interaction

References

model of nervous system disease

is ameliorated by Pu^r1

(Talsma et al., 2014)

is ameliorated by Cyt-c1L^G9163

(Talsma et al., 2014)

is ameliorated by Dyrk2¹

(Talsma et al., 2014)

is ameliorated by Fkbp59^EY03538

(Talsma et al., 2014)

is ameliorated by Gαo^MI00833

(Talsma et al., 2014)

is ameliorated by Sec15²

(Talsma et al., 2014)

is ameliorated by cact⁷

(Talsma et al., 2014)

is ameliorated by pain^EP2451

(Talsma et al., 2014)

is ameliorated by scramb2^EY01180

(Talsma et al., 2014)

is ameliorated by slmb⁰⁰²⁹⁵

(Talsma et al., 2014)

is ameliorated by spz5^e03444

(Talsma et al., 2014)

Comments on Models/Modifiers Based on Experimental Evidence ( 0 )

Disease-implicated variant(s)

Phenotypic Data

Phenotypic Class

abnormal locomotor behavior | dominant

(Ashmore et al., 2009)

abnormal neuroanatomy | dominant

(Ashmore et al., 2009)

bang sensitive | dominant | heat sensitive

(Ashmore et al., 2009)

bang sensitive | dominant | progressive | heat sensitive

(Ashmore et al., 2009)

bang sensitive | heat sensitive (with Atpα^CJ7)

(Ashmore et al., 2009)

lethal

(Ashmore et al., 2009)

lethal (with Atpα^CJ4)

(Ashmore et al., 2009)

lethal (with Atpα^CJ5)

(Ashmore et al., 2009)

lethal (with Atpα^CJ6)

(Ashmore et al., 2009)

lethal (with Atpα^CJ12)

(Ashmore et al., 2009)

lethal (with Atpα^CJ13)

(Ashmore et al., 2009)

lethal (with Atpα^DTS1R1)

(Ashmore et al., 2009)

lethal (with Atpα^DTS2R3)

(Ashmore et al., 2009)

partially lethal - majority die | heat sensitive (with Atpα^CJ7)

(Ashmore et al., 2009)

short lived | dominant

(Ashmore et al., 2009)

viable (with Atpα^CJ7)

(Ashmore et al., 2009)

Phenotype Manifest In

adult brain

(Ashmore et al., 2009)

Detailed Description

Statement

Reference

Heterozygous adults are short lived, as compared to controls.

(Ashmore et al., 2009)

External Data

Linkouts

Interactions

Show genetic interaction network for Enhancers & Suppressors

Phenotypic Class

Phenotype Manifest In

Additional Comments

Genetic Interactions

Statement

Reference

Xenogenetic Interactions

Statement

Reference

Complementation and Rescue Data

Comments

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

ATPalpha^CJ10

(Talsma et al., 2014, Ashmore et al., 2009)

Atpα^CJ10

Name Synonyms

Secondary FlyBase IDs

References (3)

Report Sections

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