Special

DmeALTD0004344-2/2 @ dm6

Alternative 5'ss

Gene
FBgn0035533 | Cip4
Description
The gene Cdc42-interacting protein 4 is referred to in FlyBase by the symbol DmelCip4 (CG15015, FBgn0035533). It is a protein_coding_gene from Dmel. It has 12 annotated transcripts and 12 polypeptides (10 unique). Gene sequence location is 3L:4322491..4364102. Its molecular function is described by: GTPase activating protein binding; lipid binding; phospholipid binding; protein binding. It is involved in the biological process described with 13 unique terms, many of which group under: macromolecule localization; plasma membrane organization; membrane organization; mesoderm development; germ cell development. 36 alleles are reported. The phenotypes of these alleles manifest in: multicellular structure; organism; cell junction; cellular anatomical entity; integumentary system. The phenotypic classes of alleles include: increased mortality during development; phenotype; increased mortality; neuroanatomy defective. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of high expression to a trough of moderate expression. Peak expression observed within 00-18 hour embryonic stages, during early pupal stages.
Coordinates
chr3L:4324284-4324996:-
Coord C1 exon
chr3L:4324922-4324996
Coord A exon
chr3L:4324862-4324921
Coord C2 exon
chr3L:4324284-4324447
Length
60 bp
Sequences
Splice sites
5' ss Seq
CGGGTACAC
5' ss Score
3
3' ss Seq
TCCATGGTGAAATCCAGCAGTTC
3' ss Score
-1.39
Exon sequences
Seq C1 exon
ACATTCCAATGGCAGTGCCGATGACCATCATGATGATGGCGACGACCAGCCCGATGATGCTGGCAGCTTAAGCAG
Seq A exon
GTCAGATTCTGAGGATAATGTGGCGCAAATACAAAATGGGCATAATAATAACAATAACGG
Seq C2 exon
TTCGGCAAGTCCCGAGAGTGGCCTTGGCACTTCGCACACATCCCTGCCAGGATCAGGACAGGGCAGCGCCAACGAAAACGCGATTGGCGAGGATACCTACTATGAAACGGAAGTGGAGACCCTTAATCCAGTGGGAAAATGTCGTGCCCTGTATCCATTTGAAG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0035533-23-19,24-19-2/2
Average complexity
Alt5
Mappability confidence:
NA
Protein Impact

Protein isoform when splice site is used (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=0.925
Domain overlap (PFAM):

C1:
PF0157614=Myosin_tail_1=PD(7.8=34.6)
A:
NA
C2:
PF0157614=Myosin_tail_1=PD(2.0=5.4),PF0001823=SH3_1=PU(13.5=12.5)


Main Inclusion Isoform:
FBpp0112051


Main Skipping Isoform:
FBpp0300522


Other Inclusion Isoforms:
FBpp0073195, FBpp0297491, FBpp0300521


Other Skipping Isoforms:
FBpp0297231, FBpp0297232, FBpp0297233, FBpp0297492, FBpp0305747, FBpp0305748
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:
CCGATGATGCTGGCAGCTTAA
R:
AGGGTCTCCACTTCCGTTTCA
Band lengths:
148-208
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)