DmeEX0009490 @ dm6
Exon Skipping
Gene
FBgn0013733 | shot
Description
The gene short stop is referred to in FlyBase by the symbol Dmelshot (CG18076, FBgn0013733). It is a protein_coding_gene from Dmel. It has 23 annotated transcripts and 23 polypeptides (21 unique). Gene sequence location is 2R:13864237..13942110. Its molecular function is described by: microtubule binding; actin binding; protein binding; calcium ion binding; structural molecule activity. It is involved in the biological process described with 23 unique terms, many of which group under: cytoplasmic microtubule organization; wound healing; branching involved in open tracheal system development; cilium organization; regulation of microtubule polymerization or depolymerization. 114 alleles are reported. The phenotypes of these alleles manifest in: membrane-bounded organelle; endocuticle; cellular anatomical entity; stomodeal invagination late; embryonic/larval integumentary system. The phenotypic classes of alleles include: lethal; increased mortality; phenotype; increased mortality during development. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of high expression to a trough of moderate expression. Peak expression observed within 18-24 hour embryonic stages.
Coordinates
chr2R:13917118-13917910:-
Coord C1 exon
chr2R:13917849-13917910
Coord A exon
chr2R:13917566-13917625
Coord C2 exon
chr2R:13917118-13917207
Length
60 bp
Sequences
Splice sites
3' ss Seq
GAATTTCCTGCGATTTTCAGACC
3' ss Score
6.09
5' ss Seq
TCTGTAAGT
5' ss Score
7.96
Exon sequences
Seq C1 exon
ACGAACGCGATGCCATTCAGAAGAAGACTTTCACAAAATGGGTTAACAAACATCTGAAAAAG
Seq A exon
ACCTATACTATGCTACATGTTTGTGTAACCACAAATGGCATACCCTGTTGTTCTCAGTCT
Seq C2 exon
GCCAATCGTCGTGTGGTGGACTTGTTCGAAGATCTGCGCGATGGTCACAATTTACTTTCACTCCTGGAGGTGCTATCTGGCGAACACCTG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0013733_MULTIEX4-2/2=C1-C2
Average complexity
C1
Mappability confidence:
100%=100=100%
Protein Impact
Alternative protein isoforms (No Ref)
No structure available
Features
Disorder rate (Iupred):
C1=0.019 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF0030726=CH=PU(12.9=61.9)
A:
PF0030726=CH=FE(15.7=100)
C2:
PF0030726=CH=FE(28.7=100)
Main Inclusion Isoform:
FBpp0293390

Main Skipping Isoform:
FBpp0086745

Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
FBpp0086742, FBpp0086743, FBpp0086744, FBpp0271730, FBpp0271731, FBpp0271732, FBpp0271733, FBpp0271734, FBpp0290806, FBpp0290807, FBpp0293389
Associated events
Conservation
Human
(hg38)
No conservation detected
Human
(hg19)
No conservation detected
Mouse
(mm10)
No conservation detected
Mouse
(mm9)
No conservation detected
Rat
(rn6)
No conservation detected
Cow
(bosTau6)
No conservation detected
Chicken
(galGal4)
No conservation detected
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
ACGCGATGCCATTCAGAAGAA
R:
AGCACCTCCAGGAGTGAAAGT
Band lengths:
132-192
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)