DmeEX6006338 @ dm6
Exon Skipping
Gene
FBgn0032252 | loh
Description
The gene lonely heart is referred to in FlyBase by the symbol Dmelloh (CG6232, FBgn0032252). It is a protein_coding_gene from Dmel. It has 4 annotated transcripts and 4 polypeptides (3 unique). Gene sequence location is 2L:10442534..10450080. Its molecular function is described by: peptidase activity. It is involved in the biological process described with: positive regulation of extracellular matrix assembly; larval heart development. 25 alleles are reported. The phenotypes of these alleles manifest in: embryonic/larval heart; embryonic/larval cardial cell; embryonic/larval pericardial cell; embryonic/larval alary muscle. The phenotypic classes of alleles include: lethal - all die during P-stage; viable; lethal - all die before end of larval stage; short lived; cell shape defective. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderately high expression to a trough of extremely low expression. Peak expression observed within 12-24 hour embryonic stages.
Coordinates
chr2L:10447781-10449299:+
Coord C1 exon
chr2L:10447781-10447982
Coord A exon
chr2L:10448049-10448230
Coord C2 exon
chr2L:10448292-10449299
Length
182 bp
Sequences
Splice sites
3' ss Seq
TCTCTTTCGTGGAATTCCAGTCC
3' ss Score
4.2
5' ss Seq
ATGGTAGAG
5' ss Score
1
Exon sequences
Seq C1 exon
GCAGTGCAAGCCAGTGGCGAAATCGATGGATTGTATGCGCACAGTGGATCCGTGAGCTGTGGTGGATTACTTTGCCGGCCAGTTACGGGCATCTTTACCAGAAATCCTCTGCCGGAACATGCCTATATACATGTTACCACATTGCCAGTGGGTGCCTCCAATATTTCGATAACTGAACTTAAGAATAGCATCAACTTGCTGG
Seq A exon
TCCTGCGCACCTCCAATGAGCTGGCCATTTTCAATGGAGAGAACACTGTCTCGGAGAGCGGATCCTACGAAGCGGTTGGTGCTGTCTTCGATTATCATCGAATCGACGGAGCTGAGGACAGCAATGGGGTGACCGAGTGGATAACGAGTATTGGACCCATTCGGGATTCATTGCAACTTATG
Seq C2 exon
GTTTTCACCAAGTCAGCCAATAATACTGGCGTGAAGTACGAGTACATGCTGCCCATAGTATCCGAGTCCGAGGAGAACGAGATGTCGCTGGAGAGCAGCGATGGCCTGTTGAGATCCGGTATGGAGGACACCAGTTCATCCAGTAGCTCGCGGGCGGGACGCAAACGTATTTTTAATTGGAAAGTAATTGGGTTCAGTAGTTGCACGAAATCCTGTGGCGGCGGCACGCAGACACCCATCATCCGTTGCATTCGAAAGAATCCATTGCGGTATTACTCGCAGCGACGTTGCACGCATTCCGTGAAACCGGTGTTGAACGAGAACCTATTGCACTGCAACACGCAACCCTGTCCGGCGTATTGGAGATTTGACGATTGGGGCGAGTGTCGCTGCTCGTCGAGCGGCGGTCTGCGTCGCAGGGAGGTTAGCTGTGTCCAGGAATTGGCTTCCGGACTGGTCATACACGTCGATAAGGCCGCCTGCATGGAGGATCAGCCACC
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0032252-'7-9,'7-8,8-9=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=0.104
Domain overlap (PFAM):
C1:
PF059869=ADAM_spacer1=PU(34.7=61.8)
A:
PF059869=ADAM_spacer1=FE(49.6=100)
C2:
PF059869=ADAM_spacer1=PD(14.0=5.1),PF0009014=TSP_1=WD(100=15.2),PF0009014=TSP_1=PU(10.2=1.8)
Main Inclusion Isoform:
FBpp0079619
Main Skipping Isoform:
NA
Other Inclusion Isoforms:
FBpp0293074, FBpp0307931
Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCGTGAGCTGTGGTGGATTAC
R:
TCTCCAGCGACATCTCGTTCT
Band lengths:
247-429
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)