Flygut: an atlas of the Drosophila adult midgut

Mouche Logo lab lemaitre Bbcf logo

Home Overview of gut regions Anatomy Histology Transgene expression mapping Gene expression
Search expression data by gene:
Gene name mus312
Flybase description The gene mutagen-sensitive 312 is referred to in FlyBase by the symbol Dmel\mus312 (CG8601, FBgn0002909).
Expression data along the gut
    Crop Cardia/R1 R2 R3 R4 R5 Hindgut Full gut
    Ratio gene/RPL42 -16.2003 -8.1024 -15.74458 -13.9264 -25.310065 -14.4056 -9.42994 -19.948319
    Affimetrix absolute value 4.402 4.614 4.253 4.649 4.172 4.715 5.353 3.972
    Affymetric present call in "x" number of chips 3 3 3 3 1 3 3 2
Intestinal gene expression in different physiological conditions
Ecc15: flies orally infected with Erwinia carotovora carotovora 15.
Pe: flies orally infected with Pseudomonas entomophila.
Pe gacA: flies orally infecte with Pseudomonas entomophila gacA.
For methods and description, see Buchon et al. 2009, Cell Host Microbe, and Chakrabarti et al. 2012, Cell Host Microbe.
Gene details (from Flybase) It is a protein_coding_gene from Drosophila melanogaster.
There is experimental evidence that it has the molecular function: protein binding.
There is experimental evidence that it is involved in the biological process: meiotic chromosome segregation; reciprocal meiotic recombination; mitotic cell cycle G2/M transition DNA damage checkpoint; resolution of meiotic recombination intermediates.
9 alleles are reported.
The phenotype of these alleles is annotated with: presumptive oocyte.
It has 2 annotated transcripts and 2 annotated polypeptides.
Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderately high expression to a trough of moderate expression.
Peak expression observed within 00-06 hour embryonic stages.
This gene is annotated by FlyBase as a dicistronic gene, meaning that some or all of its transcripts encode two or more polypeptide-coding open reading frames (ORFs) , with each ORF assigned to a different gene.
The distribution of RNA-Seq coverage data amongst the different encoded genes cannot be determined.
.