DmeEX0009739 @ dm6
Exon Skipping
Gene
FBgn0261041 | stj
Description
The gene straightjacket is referred to in FlyBase by the symbol Dmelstj (CG12295, FBgn0261041). It is a protein_coding_gene from Dmel. It has 4 annotated transcripts and 4 polypeptides (3 unique). Gene sequence location is 2R:13805794..13819571. Its molecular function is described by: voltage-gated calcium channel activity. It is involved in the biological process described with 7 unique terms, many of which group under: neuromuscular junction development; synaptic signaling; macroautophagy; divalent metal ion transport; detection of stimulus. 31 alleles are reported. The phenotypes of these alleles manifest in: cell component; synapse; organ system; somatic cell; cell. The phenotypic classes of alleles include: flightless; stress response defective; some die during embryonic stage; phenotype. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderate expression to a trough of very low expression. Peak expression observed within 12-24 hour embryonic stages, during early larval stages, at stages throughout the pupal period, in adult male stages.
Coordinates
chr2R:13807899-13813880:+
Coord C1 exon
chr2R:13807899-13808175
Coord A exon
chr2R:13810753-13810836
Coord C2 exon
chr2R:13813800-13813880
Length
84 bp
Sequences
Splice sites
3' ss Seq
ATTGTTTTTTTCATTAATAGACC
3' ss Score
7.89
5' ss Seq
GCGGTAAGT
5' ss Score
11.37
Exon sequences
Seq C1 exon
CGAATCATGGACACGGCTGAGAACACGGCGTTGTCGCATCAGAACGACATGGCGGACAAGATGTTCTCCTATTATAGTGCCAAGGAGATGCTGGAGCCCGGCGATCCAGTCCCGCCCATTCCCACACCGGCTCCCGACATGGACAAGGATATAGGCGAGCCGCTGATCTACGTCCAGCCGAAGGTGGTGGTGTTGGAACCGCGTCCGGAATTCCACAATACTCCGGTCAACTTTAGCGTCAGTTCGGTCCACGTGCCAGTCAATGTGTTCGATCGAG
Seq A exon
ACCTGGAACCAGCCGGTGGACTCGAATGTGTACCAATTTATGACCACCGTATCGATGCCCATCTACGATCGTCGCGAGAACGCG
Seq C2 exon
ACTAGGATTGCGAATATATTGGGCGTGGCCGGCACGGATGTGCCCATCAATGAAATCAAAAAGCTGCTGTCGCCGTTCACG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0261041_MULTIEX1-4/6=C1-C2
Average complexity
C3
Mappability confidence:
100%=100=100%
Protein Impact
Alternative protein isoforms (Ref)
No structure available
Features
Disorder rate (Iupred):
C1=0.172 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF083996=VWA_N=PU(64.4=93.5)
A:
PF0274313=Cache_1=PU(31.3=92.9)
C2:
PF0274313=Cache_1=FE(31.3=100)
Main Inclusion Isoform:
FBpp0293237
Main Skipping Isoform:
NA
Other Inclusion Isoforms:
FBpp0086757, FBpp0293238
Other Skipping Isoforms:
NA
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:
GCTCCCGACATGGACAAGGAT
R:
GCCACGCCCAATATATTCGCA
Band lengths:
177-261
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)