FlyBase Recombinant Construct Report: P{UAS-tsr.V7M.3HA}

UAS regulatory sequences drive expression of tsr (from the LD06785 cDNA clone), mutated to carry a V7M amino acid substitution. This mutation is equivalent to the same amino acid change in the orthologous human CFL2 gene, a variant identified in patients with less severe cases of nemaline myopathy. The coding sequence is tagged at the C-terminal end with 3xTag:HA.

(Balakrishnan et al., 2020)

Sequence Data

Sequence (FB)

Associated Sequence Data

DDBJ / EMBL / GenBank

DNA Sequence

Extent

Segments and Size

Total Size

Left end

Right end

Segments

Num

Orientation

Symbol

Reference

Phenotypic Data

Component Allele

Phenotypic Data

tsr^{V7M.UAS.Tag:HA}

Phenotypic Class Phenotype Manifest In Detailed Description

Expression Data

Reporter Expression

Additional Information

Statement

Reference

Marker for

Reflects expression of

Reporter construct used in assay

Progenitors and Descendants

progenitor(s)

descendant(s)

Comments

Stocks (0)

Stocks containing insertion(s) of this recombinant construct

External Crossreferences and Linkouts ( 0 )

Synonyms and Secondary IDs (3)

Reported As

Symbol Synonym

DmCFL^V7M::HA

(Balakrishnan et al., 2020)

P{UAS-tsr.V7M.3HA}

(FlyBase, 1992-)

UAS-tsr^V7M::3HA

(Balakrishnan et al., 2020)

Secondary FlyBase IDs

References (3)

Report Sections

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