DmeEX6018439 @ dm6
Exon Skipping
Gene
FBgn0037280 | CG1126
Description
The gene Bardet-Biedl syndrome 5 is referred to in FlyBase by the symbol DmelBBS5 (CG1126, FBgn0037280). It is a protein_coding_gene from Dmel. It has 2 annotated transcripts and 2 polypeptides (1 unique). Gene sequence location is 3R:4816318..4817776. Its molecular function is described by: phosphatidylinositol-3-phosphate binding. It is involved in the biological process described with: cilium assembly; intracellular transport. 2 alleles are reported. No phenotypic data is available. The phenotypic class of alleles includes: viable. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of low expression to a trough of extremely low expression. Peak expression observed within 06-18 hour embryonic stages.
Coordinates
chr3R:4816487-4817189:+
Coord C1 exon
chr3R:4816487-4816635
Coord A exon
chr3R:4816696-4816891
Coord C2 exon
chr3R:4816952-4817189
Length
196 bp
Sequences
Splice sites
3' ss Seq
AATTACATTTCCCTAAGAAGCCA
3' ss Score
0.23
5' ss Seq
TCAGTGAGG
5' ss Score
2.91
Exon sequences
Seq C1 exon
GCACAAGAACCTGCGGAGCGGAGAACGAGTGCTCGACTACATTTACCACATCGAAGACAGCAAAGGAAATCCGGGGGACACTGGTCGCCTGATGGTAACCAATTTGCGAATTATATGGCACTCGCTGGTCCACAAGAAGTACAATCTGT
Seq A exon
CCATTGGCTATGCTCGGATTGGCAACACCAACACTCGGGTAGTTCATATGCACTCCAAAGCAAGGATAGCCAGCCAGGCCCTCTACATCCTGGCGGTAAGCAACGAGACCCGCTTTGAGTTCCTTTTCACCGACGTATCTGGGGAAACGTCGCGTCGCGATCAGCCGATCTTCGCCAGCGTGTTCGACGTATATCA
Seq C2 exon
CCTTTATCAGCGTACTTATCTCTACCGCGACCTGAAGCTGCGCGGAGCCATCGTTCAAGCGGGTCAACTGGTTATCCTACCAGATGAGGAGGTCTTTAGCCATGTGCAGGGCGTGTGGAATTTGTCTAGCGACCAGGGCAACCTGGGCAGCTTCGTGGTAACCAATATTCGGCTGGTGTGGTTTGCAGATGCCAACGAGACCTTCAACATCAGTCTACCATATCTACAGATTGAGAGT
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0037280-'1-2,'1-1,2-2=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=0.000
Domain overlap (PFAM):
C1:
PF072896=DUF1448=FE(14.0=100)
A:
PF072896=DUF1448=FE(18.3=100)
C2:
PF072896=DUF1448=FE(22.2=100)
Main Inclusion Isoform:
FBpp0078512

Main Skipping Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CACTGGTCGCCTGATGGTAAC
R:
CCACACCAGCCGAATATTGGT
Band lengths:
252-448
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)