DmeEX6000980 @ dm6
Exon Skipping
Gene
FBgn0040918 | schlank
Description
The gene schlank is referred to in FlyBase by the symbol Dmelschlank (CG3576, FBgn0040918). It is a protein_coding_gene from Dmel. It has 3 annotated transcripts and 3 polypeptides (1 unique). Gene sequence location is X:6257668..6267228. Its molecular function is described by: N-acyltransferase activity; DNA binding; sphingosine N-acyltransferase activity. It is involved in the biological process described with: SREBP signaling pathway; triglyceride metabolic process; negative regulation of lipid catabolic process; positive regulation of lipid biosynthetic process; ceramide biosynthetic process. 30 alleles are reported. The phenotypes of these alleles manifest in: prothoracic gland; terminal bouton; wing; endosome; trichogen cell. The phenotypic classes of alleles include: visible; lethal; increased mortality during development; phenotype. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of high expression to a trough of moderate expression. Peak expression observed at stages throughout embryogenesis, during late larval stages, during early pupal stages.
Coordinates
chrX:6259312-6267228:-
Coord C1 exon
chrX:6266407-6267228
Coord A exon
chrX:6259604-6259724
Coord C2 exon
chrX:6259312-6259533
Length
121 bp
Sequences
Splice sites
3' ss Seq
AAACTCAATATTACTTGCAGTTT
3' ss Score
3.48
5' ss Seq
AAGGTGAGT
5' ss Score
10.47
Exon sequences
Seq C1 exon
AATTCGATTCGGCGGTTTTTGTTTTTTTGCCAGTGTGTGTTTGTGCTACGCTGTGAGTGTGCATTAGTGTCCGGTGCTCCTGTTGTTGTTCTTGTTGCTGTTGTTGTCGCTTATTGTTGTTCTTGCTGTTATTGTTGCTGTTGTTCGCAAGGCACAATAACACAGGCTCATACAATTGCGAATATTTAGAAAAAGCAAAGCATATACATATGTGACAACAAACGCCAAGGAAAAACTGGAAAGCTAAGCAAAGGAAAACCAAGAAAAAGAAAACAAACAATTGAGAAATTAAGAAGCGGCAACTGAAGCAGCAACATGGACATATTGAATGAGTTCAGCAATGTATTCTGGAGTACGCACATTTGGCTGCCGCCGAACACAACCTGGGCGGACATTGCGCCCGGCTCGCGTCCAGATGTGGTGCACGCCAACTACAAGGACCTCATATGGCCCATTCCATTCGCCGCTGTTGTCATGCTGGTCCGCTACACGCTGGAGCG
Seq A exon
TTTCTGGATATCGCCCGTAGGCAAATCACTTGGCATACGTAGTTCTAGGCCTAAGAAAGCGGCAAATGTTCCTATTCTGGAGAAGACCTATGCCAAATCGACGCGATTGGACAAGAAAAAG
Seq C2 exon
CTGGTTCCGCTGTCCAAGCAGACGGATATGAGCGAGCGCGAAATCGAGCGCTGGTGGCGTCTACGCAGGGCCCAGGATAAACCGTCAACGCTGGTGAAGTTCTGCGAGAACACGTGGCGTTGCATCTACTATCTGTACAGCTTCATCTTTGGCGTGATCGTGCTGTGGGACAAGCCCTGGTTTTGGGATGTGAAGAGCTGCTGGTACGGCTACCCGCATCAG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0040918-'4-7,'4-6,11-7=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
NO
A:
PF0004624=Homeobox=PU(48.2=65.9)
C2:
PF0004624=Homeobox=PD(48.2=36.5),PF0379811=TRAM_LAG1_CLN8=PU(21.2=55.4)
Main Inclusion Isoform:
FBpp0070898

Main Skipping Isoform:
NA
Other Inclusion Isoforms:
FBpp0070899
Other Skipping Isoforms:
NA
Associated events
Conservation
Mouse
(mm9)
No conservation detected
Chicken
(galGal4)
No conservation detected
Chicken
(galGal3)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CTGGAGTACGCACATTTGGCT
R:
AGAACTTCACCAGCGTTGACG
Band lengths:
256-377
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)