DmeEX0009481 @ 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:13882401-13901572:-
Coord C1 exon
chr2R:13901437-13901572
Coord A exon
chr2R:13900366-13900449
Coord C2 exon
chr2R:13882401-13882547
Length
84 bp
Sequences
Splice sites
3' ss Seq
TACCCCTCGAAAACCCATAGAAA
3' ss Score
2.73
5' ss Seq
AAGGTAAAA
5' ss Score
8.38
Exon sequences
Seq C1 exon
AATGCGCTCATGCGAGACGGCTATCGGGCTTATGAAGAATCTCCAGTCGAGCGTGCAAGTGGAGGAATCATGGGTGGATGGCACCACGGAGCGACTGTCTGCCATGCCCACCGCCACTTCGGCATACGAACTAGAT
Seq A exon
AAACTGCTCGGAGCTGCAATCGAACGAAAACCAAAAATCGAAAATGTCAACGTGGCTGGAGGACGACTTATACGCGAAGCTAAG
Seq C2 exon
CAAGCAGTATTCGAGAAGTTCAACATGTGCGAAGAGAATGTCAACGATCTGTTGAAATGGGTTACCACTGTGGAACAGAAAATCTCAAGTGTCGGCGGACCTCGTGAAAAGATTGATGAGTTACGCAACCAGATTAATGCCCTTAAG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0013733_MULTIEX1-1/5=C1-C2
Average complexity
ME(1-3[100=100])
Mappability confidence:
100%=100=100%
Protein Impact
Alternative protein isoforms (Ref)
No structure available
Features
Disorder rate (Iupred):
C1=0.137 A=0.000 C2=0.002
Domain overlap (PFAM):
C1:
PF0043516=Spectrin=PD(4.5=10.9)
A:
NO
C2:
PF0043516=Spectrin=PU(37.3=89.8)
Main Inclusion Isoform:
FBpp0086747

Main Skipping Isoform:
FBpp0086744

Other Inclusion Isoforms:
FBpp0086742, FBpp0086743, FBpp0086745, FBpp0271730, FBpp0271731, FBpp0271732, FBpp0271733, FBpp0271734, FBpp0290806, FBpp0290807, FBpp0290808, FBpp0293387, FBpp0293388, FBpp0293389, FBpp0293390, FBpp0293392, FBpp0293393
Other Skipping Isoforms:
FBpp0086746, FBpp0291176
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GAGGAATCATGGGTGGATGGC
R:
GTCCGCCGACACTTGAGATTT
Band lengths:
175-259
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)