Special

DmeEX6018862 @ dm6

Exon Skipping

Gene
Description
The gene Alhambra is referred to in FlyBase by the symbol DmelAlh (CG1070, FBgn0261238). It is a protein_coding_gene from Dmel. It has 14 annotated transcripts and 14 polypeptides (13 unique). Gene sequence location is 3R:7094596..7124185. Its molecular function is described by: DNA-binding transcription factor activity. It is involved in the biological process described with: larval somatic muscle development; regulation of transcription, DNA-templated; haltere development; molting cycle, chitin-based cuticle; instar larval development. 88 alleles are reported. The phenotypes of these alleles manifest in: embryonic/larval somatic muscle; wing; larva; embryonic/larval nervous system; RP2 motor neuron. The phenotypic classes of alleles include: phenotype; fertile; courtship behavior defective; viable. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderately high expression to a trough of low expression. Peak expression observed within 00-18 hour embryonic stages, at stages throughout the pupal period, in adult female stages.
Coordinates
chr3R:7096292-7098483:-
Coord C1 exon
chr3R:7098319-7098483
Coord A exon
chr3R:7096887-7097346
Coord C2 exon
chr3R:7096292-7096820
Length
460 bp
Sequences
Splice sites
3' ss Seq
TCTAACCAAAATGCTTACAGCCG
3' ss Score
3.25
5' ss Seq
GAGGTGAGA
5' ss Score
7.66
Exon sequences
Seq C1 exon
TTGCCTCGCTGCTTAATTGCTTGCACCAGCTGCAGAGCGAAAACCTCCGGCTGGAGGAGCATGTGACCAGCCTGATAGCGCGACGTGATCACCTGCTGGCGGTCAATGCGCGCCTGCAGATCCCGCTGAGTACCATCGCAAGCAACACCAAGGCCGAGGCGCATG
Seq A exon
CCGCCATATCAACAACGGCAGCTCCAACAACCACAACAACAACCTCAACAACAACAGCAACATCAACTTGTACAACTTCTGTCATTTCCACAATAGCTTCCAGCGGCAACAGCAGCACCAGCACCATCGGACTCGGCAGCAGCACGAGTGCCCTTAATGCGGCCACAACAATCGCAGCAGCCGTCTCACTGGCAACAACGGCCATCAATACCACCATCCCCACCATGGCCAATAGCCGGCCAACAGTGGCTGCTGCGAGTTCCAGTGGAGTGCTCGACTATCGCGGACCAGGTGCAACCAGCAACAGCAGCAATAGCAACAGCAGCAACAATACAATTAGCAATAGTGTGAGCAACAGCAGTAGTAATCCTACAAGCTCTTCGAGTGCCAGCGTACCGCCTGCATCATCCATGTCGATCTCCGGCATGAGCATATCCAATGCAACCAATTTGGGAATGAG
Seq C2 exon
ACACGTGTCTGCAGCCCATGGATCCAACAATGCTGGGAACAGCAACAGCAGCGTTTGGAGCTTAACTGCCAGTAGCACCGTCAACAGCAACAGTTTGCATCACCAACATTCATCGCAGCAGCAGCAGCAGCATCAGGCGCAACACCAGTCGCATCCGTTGCAGCAACAGCAGCAGCAGCAGCAACAAGTGCAACATCATCTGCATCAGTCGCACCACACCAGCGCTGCTGTGGCAGCCGCTCATATGCTTGGCGTGGGAATGAGCCTGGGCGCTGGAGGTGGTGCTGCCGGTGGAATTGGACGAGGTGGGTCAGCGACAGCCATGGCTGCAACAGCAGCAACAACCACAACTACTTTTACGACCACAGCGGGCACGGGCATGGGTCAGCAGCACCACCACCCACACCCACACCAACATCCTAGCATTCAGATTCAAGTGGGTGGCGGCGGCGTTGGCGTTGACGGTTTAAGTAGCACCTCCTCCTCCTATGCGGTGCACC
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0261238-'29-18,'29-16,31-18=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=0.156 A=0.713 C2=0.940
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
NO


Main Inclusion Isoform:
FBpp0303393


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
FBpp0289721, FBpp0289722, FBpp0306735, FBpp0306736, FBpp0306737


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TACCATCGCAAGCAACACCAA
R:
CTGACCCACCTCGTCCAATTC
Band lengths:
349-809
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)