Special

DmeEX0008586 @ dm6

Exon Skipping

Gene
Description
The gene muscleblind is referred to in FlyBase by the symbol Dmelmbl (CG33197, FBgn0265487). It is a protein_coding_gene from Dmel. It has 19 annotated transcripts and 19 polypeptides (18 unique). Gene sequence location is 2R:17216549..17379376. Its molecular function is described by: RNA binding; metal ion binding; nucleic acid binding. It is involved in the biological process described with 9 unique terms, many of which group under: regulation of nucleobase-containing compound metabolic process; reproductive process; programmed cell death; apoptotic process; organic cyclic compound metabolic process. 93 alleles are reported. The phenotypes of these alleles manifest in: fascicle; larva; rhabdomere; visceral muscle; cytoskeleton. The phenotypic classes of alleles include: increased mortality during development; some die during embryonic stage; phenotype; courtship behavior defective.
Coordinates
chr2R:17265518-17351264:+
Coord C1 exon
chr2R:17265518-17266211
Coord A exon
chr2R:17275410-17276063
Coord C2 exon
chr2R:17351094-17351264
Length
654 bp
Sequences
Splice sites
3' ss Seq
CTCTTTTACTCTCATTTCAGATA
3' ss Score
10.53
5' ss Seq
AAGGTCAGT
5' ss Score
8.68
Exon sequences
Seq C1 exon
AAAAGTTTTAGCCTACAACTCTAGAAACGCGGAAAAATTTGTCAAAAATACAACTAAAAAAACAACAACGCGAGTGCACGTGTATGTGAGGTGCTCAGTAAGAGTGTTTGCGTGTGTTCGTTTCTGTGTGTGACAGATAATAAAAGGAGAAAAAAAGAAGTTGTCGAAAGTCGTTCGTGAAAATTCAAGAAAAATAGTGCAAGCGCTGCAGGGAAATTGTCCGGAAAAATCGCAAAATCCATTGTTTTTAGCCGGCATCTTAAAAACCAACGATAACAACAGCTTCTGCAACAACGCGCGTGTTTAGTTCACACACACACCACGGAGCGTCGAGAAAAAAAGGTTAAAAATACATTTTCAATTCACCATCGGCGTAAAAGTAAAACAATAAACAAATACAAGAAAATAAAACAGCAGCCGCTTTTTCACCCAACAACAACAATTTCAACAACTTCAACTTCGCCAGCAGCAACAACAACAAGTCAGCTGGACAACCGAAG
Seq A exon
ATAATGTAAACTCAGCTTACACACAAAAAAGCAGTAAAATATAAAATACAAAAATTAACAGCTGCGTTTATCTATAGATATATATATACACATCTATATATTTGAATAAGCGTTCGATTTGAATCAAAATTATAGCCCAAGCTATCAGCTACCCCCACAAGCTTTGTACTCCACAAAAACGCTAACGAGCAAAATCGATAAAGACCAGATAGCAAATGAAATCATACCATCTGCCATAGATCTATGCTATAAACATATATAGGTGCTGATCTGTGCTCTTGAATTTAGTGTTTTTTGTGTGTGCGTGTCGCGAGAGGAGCACTCAAAACCAAAAAAAAAAAAAAAAACGTATAGTAAAACAAAAAACTATCTCTAGTCGCTAGGCTATAACTATACAAACTCCAGCTATCCCAGATCCAGATCCGTAAACAGCAAATAGTTATATATCTATAACCCCAAAATACGATGGCCAACGTTGTCAATATGAACAGCCTGCTCAACGGCAAGGATTCGCGCTGGCTGCAATTGGAGGTCTGTCGCGAGTTCCAGCGCAACAAATGCTCGCGCCAGGACACCGAATGCAAGTTCGCCCATCCCCCGGCCAACGTGGAGGTCCAGAACGGCAAGGTCACCGCCTGCTACGACAGCATCAAG
Seq C2 exon
GGCCGCTGTAATCGTGATAAACCGCCGTGCAAATACTTTCATCCACCACAGCATCTGAAGGATCAGTTATTGATAAATGGACGCAATCATTTGGCCCTCAAGAATGCACTGATGCAACAGATGGGCATCGCGCCCGGCCAACCGGTCATATCGGGCCAAGTGCCAGCCGTG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0265487-'7-18,'7-11,10-18
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref, Alt. ATG (>10 exons))

No structure available
Features
Disorder rate (disopred):
  C1=NA A=0.232 C2=0.286
Domain overlap (PFAM):

C1:
NA
A:
NO
C2:
NO


Main Inclusion Isoform:
FBpp0307871


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
FBpp0086143, FBpp0086144, FBpp0086146, FBpp0297556, FBpp0297558, FBpp0297559, FBpp0297561, FBpp0301759, FBpp0301760, FBpp0302029, FBpp0307872, FBpp0307873


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CAACAACGCGCGTGTTTAGTT
R:
CGATGCCCATCTGTTGCATCA
Band lengths:
342-996
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)