Special

DmeEX0008855 @ dm6

Exon Skipping

Gene
FBgn0016920 | nompC
Description
The gene no mechanoreceptor potential C is referred to in FlyBase by the symbol Dmel ompC (CG11020, FBgn0016920). It is a protein_coding_gene from Dmel. It has 6 annotated transcripts and 6 polypeptides (5 unique). Gene sequence location is 2L:5346200..5365760. Its molecular function is described by: cation channel activity; mechanosensitive ion channel activity; calcium channel activity; ion channel activity; ankyrin binding. It is involved in the biological process described with 13 unique terms, many of which group under: response to abiotic stimulus; multicellular organismal process; nervous system process; system process; response to external stimulus. 31 alleles are reported. The phenotypes of these alleles manifest in: adult prothoracic segment; mechanosensory chaeta; cell projection; larval dorsal multidendritic neuron ddaA; adult neuron. The phenotypic classes of alleles include: sensory perception defective; behavior defective; some die during larval stage; phenotype. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderate expression to a trough of extremely low expression. Peak expression observed within 18-24 hour embryonic stages.
Coordinates
chr2L:5362583-5364426:+
Coord C1 exon
chr2L:5362583-5362812
Coord A exon
chr2L:5363656-5363784
Coord C2 exon
chr2L:5364309-5364426
Length
129 bp
Sequences
Splice sites
3' ss Seq
AAAAACCTATGAAATACTAGGCC
3' ss Score
1.23
5' ss Seq
AAGGTAAAA
5' ss Score
8.38
Exon sequences
Seq C1 exon
TGCGCATGCATCCGATTAACTCGTTCGAGTTGTTGTTCTTCGCCGTGTTCGGACAAACGACGACCGAGCAAACGCAAGTTGACAAAATCAAAAATGTAGCCACGCCCACTCAACCGTATTGGGTTGAGTACCTGTTCAAAATTGTCTTTGGCATTTACATGTTGGTGTCGGTGGTTGTGCTCATTAACCTGCTGATTGCTATGATGTCAGACACCTATCAACGCATTCAG
Seq A exon
GCCCAATCCGACATCGAGTGGAAATTTGGCTTGTCCAAGCTTATACGCAATATGCATCGCACCACAACAGCGCCATCGCCGCTTAATTTAGTTACCACCTGGTTTATGTGGATCGTCGAGAAGGTCAAG
Seq C2 exon
GCACGCATGAAGAAAAAGAAGCGTCCAAGTCTGGTTCAGATGATGGGAATACGTCAGGCCAGTCCGCGTACCAAAGCCGGCGCCAAGTGGCTGTCGAAGATCAAGAAAGGTGAGACAT
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0016920_MULTIEX1-4/4=3-C2
Average complexity
C1
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (No Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.021 A=0.000 C2=0.052
Domain overlap (PFAM):

C1:
PF0052026=Ion_trans=PD(35.1=51.5)
A:
NO
C2:
NO


Main Inclusion Isoform:
FBpp0309913


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
FBpp0289289, FBpp0293383


Other Skipping Isoforms:
NA
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:
AAAAATGTAGCCACGCCCACT
R:
TGATCTTCGACAGCCACTTGG
Band lengths:
244-373
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)