Special

DmeALTA0009263-1/2 @ dm6

Alternative 3'ss

Gene
Description
The gene still life is referred to in FlyBase by the symbol Dmelsif (CG34418, FBgn0085447). It is a protein_coding_gene from Dmel. It has 14 annotated transcripts and 14 polypeptides (12 unique). Gene sequence location is 3L:5657913..5749599. Its molecular function is described by: Rac guanyl-nucleotide exchange factor activity. It is involved in the biological process described with 11 unique terms, many of which group under: sensory perception of light stimulus; sensory system development; activation of GTPase activity; regulation of molecular function; sensory perception. 26 alleles are reported. The phenotypes of these alleles manifest in: retinal pigment cell; eye; mesothoracic tergum; chaeta; interommatidial bristle. The phenotypic classes of alleles include: cell number defective; behavior defective; locomotor behavior defective; 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 12-24 hour embryonic stages, during early larval stages, during late pupal stages, in adult male stages.
Coordinates
chr3L:5731440-5734609:+
Coord C1 exon
chr3L:5731440-5731636
Coord A exon
NA
Coord C2 exon
chr3L:5734466-5734609
Length
0 bp
Sequences
Splice sites
5' ss Seq
CAAGTAAGT
5' ss Score
10.08
3' ss Seq
GATTTTGTCGTTCACCCCAGGAA
3' ss Score
8.84
Exon sequences
Seq C1 exon
ATGGCACTAGCAAGGATTTGTACTCGCCGGAGGCTGAAAGCTCGCCGGCCACCTCCTTTGTGGATCCTGCCGCAATGGCCGCCCAGCTGGCGGTGGGCGGCGTGGGAGGCGTGGTCGTGGGCGGACTGGGCGTGGCCAAGCCAACGTCGCGTACGAGCAGCTTTGAGATTGAGAATCTGCTAAAGACCGCGGAGCAA
Seq A exon
NA
Seq C2 exon
GAAACGCGGAAATCGAGCCCAACCGGCTCGGTCACCTCATCGGTGTCGACCACGGCATTAACACCATCACGGCAGCTGACCGATGCGGAGAAGCTGCGCAAAGTCGTCATGGAGCTGGTGGACACGGAACGCACCTATGTGAAG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0085447-40-40,40-39-1/2
Average complexity
Alt3
Mappability confidence:
NA
Protein Impact

Protein isoform when splice site is used (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.367 A=NA C2=0.515
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0062115=RhoGEF=PU(6.8=27.1)


Main Inclusion Isoform:
FBpp0303156


Main Skipping Isoform:
FBpp0303159


Other Inclusion Isoforms:
FBpp0111620, FBpp0111621, FBpp0111624, FBpp0303155, FBpp0312426


Other Skipping Isoforms:
FBpp0111622, FBpp0303157, FBpp0303158, FBpp0309505, FBpp0309506, FBpp0309507
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:
GCGTACGAGCAGCTTTGAGAT
R:
TGTTAATGCCGTGGTCGACAC
Band lengths:
112-139
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)