Special

DmeEX6001375 @ dm6

Exon Skipping

Gene
FBgn0261549 | rdgA
Description
The gene retinal degeneration A is referred to in FlyBase by the symbol Dmel dgA (CG42667, FBgn0261549). It is a protein_coding_gene from Dmel. It has 12 annotated transcripts and 12 polypeptides (11 unique). Gene sequence location is X:8907068..9029476. Its molecular function is described by: diacylglycerol kinase activity; NAD+ kinase activity. It is involved in the biological process described with 14 unique terms, many of which group under: system process; nervous system process; multicellular organismal process; taxis; retina homeostasis. 67 alleles are reported. The phenotypes of these alleles manifest in: tergum; syncytium; plasma membrane bounded cell projection; Z disc; I band. The phenotypic classes of alleles include: flight defective; wild-type; increased mortality; phenotype. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderately high expression to a trough of very low expression. Peak expression observed during late pupal stages.
Coordinates
chrX:9021726-9023326:+
Coord C1 exon
chrX:9021726-9021952
Coord A exon
chrX:9022018-9022239
Coord C2 exon
chrX:9023275-9023326
Length
222 bp
Sequences
Splice sites
3' ss Seq
TTCAATGCCATCCCTTTTAGCCT
3' ss Score
6.75
5' ss Seq
CCGGTAGGA
5' ss Score
8.18
Exon sequences
Seq C1 exon
AGTGAATCCCCTGGAGAAGATGCAGTTGCACATTTTGCGCGTGACCATGCAACAGTACGAGCAGTACCACTATGACAAGGAGATGCTACGCAAATTGGCCAATAAGTTGGGTCAAATCGAAATCGAATCTCAGTGCGATTTGGAGCATGTGCGCAATATGCTCAACACCAAGTTCGAGGAATCCATCTCCTATCCAAAGGTCTCACAGGATTGGTGCTTCATCGACT
Seq A exon
CCTGCACCGCTGAGCACTACTTCCGGATCGATCGTGCCCAGGAGCATCTGCACTATATCTGCGACATTGCCATCGATGAACTGTATATCCTGGACCACGAGGCGGCCACCATGCCGCAGACACCCGATCAGGAGCGCTCCTTTGCAGCCTTCTCGCAGCGGCAGGCACAGAACGAGCGACGCCAAATGGATCAGGCCCAGGGTCGCGGCCCGGGCAGCACCG
Seq C2 exon
ATGAGGATTTGCAAATTGGCTCCAAGCCCATAAAAGTGATGAAGTGGAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0261549-'38-27,'38-26,39-27=AN
Average complexity
A_C1
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.496 C2=0.278
Domain overlap (PFAM):

C1:
NO
A:
PF127962=Ank_2=PU(1.2=1.3)
C2:
PF127962=Ank_2=PU(20.2=94.4)


Main Inclusion Isoform:
FBpp0305778


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
FBpp0291800, FBpp0291801, FBpp0291802, FBpp0291803, FBpp0291804, FBpp0291805, FBpp0305779, FBpp0310579, FBpp0310580


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTGAATCCCCTGGAGAAGATGC
R:
CTTCCACTTCATCACTTTTATGGGC
Band lengths:
276-498
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)