Special

DmeEX0006537 @ dm6

Exon Skipping

Gene
Description
The gene Spinophilin is referred to in FlyBase by the symbol DmelSpn (CG16757, FBgn0010905). It is a protein_coding_gene from Dmel. It has 12 annotated transcripts and 12 polypeptides (9 unique). Gene sequence location is 3L:2505245..2554292. Its molecular function is described by: neurexin family protein binding; actin filament binding. It is involved in the biological process described with: neuron projection development; negative regulation of presynaptic active zone assembly; calcium-mediated signaling; actin filament organization. 29 alleles are reported. The phenotypes of these alleles manifest in: presynaptic active zone; embryonic/larval neuromuscular junction. The phenotypic classes of alleles include: smell perception defective; behavior defective; viable; flightless; neuroanatomy defective; partially lethal - majority die. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of high expression to a trough of low expression. Peak expression observed within 00-06 hour embryonic stages.
Coordinates
chr3L:2511163-2512472:-
Coord C1 exon
chr3L:2512295-2512472
Coord A exon
chr3L:2511878-2511931
Coord C2 exon
chr3L:2511163-2511763
Length
54 bp
Sequences
Splice sites
3' ss Seq
ATTTGTTTTTATTTTCCCAGAGC
3' ss Score
8.45
5' ss Seq
AAGGTTTGT
5' ss Score
7.81
Exon sequences
Seq C1 exon
CCAACAAGAGGAGTACCTGCGCCGCACTCTCGACTATTCCGAGGACTCCACTCAGCCGGTTTCGGCCAACTCGAGTGTCTGCGAGGGACCCTCGAGTCCCGTCCAAGTGGAACATCCAATGGAGGTGGAGGCCACCCACTCGCAGGAGGTAGAGTCGCTCAAGCGGCTGCTACAGGAG
Seq A exon
AGCGAAATGGGTTGCCTGGTTAAAGAGGAGATTATTCAAAATCTTAAACGAAAG
Seq C2 exon
CTGGTCAAGCTCGAGACGACGGGCAATGAGAACGAGCTGCTTAGCGAGCGACTGCGGCAAAGCGAGCGGGAGCTGGGCAATATCCGGAAGGAGGCGGCCAACCTGCAGAACATGCTCCAGCAGTCGCAGGGTCAGTATATGGCGCTGGACAAGAAGTACAACAAGGCCAAGCGGCTGGTCAGGGAGTACCAGCAGCGAGAGCTGGACATGTGCCATCGCGAGGAGTTCTACCAGCAGCTGCTCCAGGAGAAGGACACCGAGTACAATGCGCTGGTGAAGAAGCTGAAGGATCGTGTGATTAATCTGGAACACGAGCTGCAGGAGACGCAGCGCAAGGCCGGTTTTCCAGTGGGCCTGCCCTACGATAGTGCCACTCTGAAGTTGACGCCCCAGATGATGCGTAAGACGCCGCCAAAGCCGCTCTTCCACAAGCTCGAGACGGAGCTGTCGGATACGGAGATATCAGATCTCTCACCCGACGGCGATGGCGTTAAGACAGC
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0010905-'17-14,'17-13,19-14
Average complexity
ME(12_18-13_19[100=97])
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.836 A=0.000 C2=0.550
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
NO


Main Inclusion Isoform:
FBpp0293163


Main Skipping Isoform:
FBpp0293162


Other Inclusion Isoforms:
FBpp0293155, FBpp0293156, FBpp0293157, FBpp0293158, FBpp0293159, FBpp0293160, FBpp0293161, FBpp0311290


Other Skipping Isoforms:
FBpp0311289
Primers PCR
Suggestions for RT-PCR validation
F:
CCACTCGCAGGAGGTAGAGTC
R:
CTTCCGGATATTGCCCAGCTC
Band lengths:
133-187
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)