Special

DmeEX0001223 @ dm6

Exon Skipping

Gene
FBgn0039830 | CG1746
Description
The gene ATP synthase, subunit C is referred to in FlyBase by the symbol DmelATPsynC (CG1746, FBgn0039830). It is a protein_coding_gene from Dmel. It has 7 annotated transcripts and 7 polypeptides (2 unique). Gene sequence location is 3R:31216145..31219630. Its molecular function is described by: proton-transporting ATP synthase activity, rotational mechanism. It is involved in the biological process described with: ATP synthesis coupled proton transport; proton transmembrane transport. 22 alleles are reported. No phenotypic data is available. No phenotypic class data is available. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of extremely high expression to a trough of very high expression. Peak expression observed during early larval stages, during late pupal stages, in stages of adults of both sexes.
Coordinates
chr3R:31217740-31219630:-
Coord C1 exon
chr3R:31219536-31219630
Coord A exon
chr3R:31218943-31219048
Coord C2 exon
chr3R:31217740-31217944
Length
106 bp
Sequences
Splice sites
3' ss Seq
CTCCGTCTATATCTTTGCAGAGC
3' ss Score
9.78
5' ss Seq
GCCGTAAGT
5' ss Score
10.11
Exon sequences
Seq C1 exon
TTTTTCCCAGCTCCCGCTGACGGCCACACTTAGCACCCCCCAAAAGTCAGCGAAATTGTCAAATTCGTTTTACTGTTGTGAAGGGTTCGTTCGAA
Seq A exon
AGCCGTGCGCTAGCTTCAATTTTGTCGTAAGCAAAACAAAAAGGAAATTCAACCGAAAATGTTCGTGTCGACAGTCTCTCGCATTGCCCCAGTTGCCAGGAGCGCC
Seq C2 exon
TTCCTCGCCAACTCCAAGCAGTACTTGCGACCATTGAGCAGCGCCATCATCAGCCAGAGCCAGACTTTGGCCGCTCAGAACACAACCCCCGTTGCATTGCTGCCACAGATCAGGTCATTCCAGACCTCGCCAGTCACGCGTGACATTGACTCGGCCGCCAAATTCATTGGTGCTGGTGCCGCAACAGTCGGTGTCGCTGGATCCG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0039830-'0-3,'0-1,13-3
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref, Alt. ATG (>10 exons))

No structure available
Features
Disorder rate (Iupred):
  C1=NA A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
NA
A:
NO
C2:
PF0013716=ATP-synt_C=PU(23.2=23.2)


Main Inclusion Isoform:
FBpp0085134


Main Skipping Isoform:
FBpp0293653


Other Inclusion Isoforms:
FBpp0085135, FBpp0085136, FBpp0293652, FBpp0297347


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CTGACGGCCACACTTAGCAC
R:
GAATTTGGCGGCCGAGTCAAT
Band lengths:
244-350
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Neural diversity
  • Neurogenesis
  • Neuronal activity
  • Splicing factor regulation (brain)
  • Splicing factor regulation (SL2)