Special

DreEX6043759 @ danRer10

Exon Skipping

Gene
ENSDARG00000098233 | TIAM2 (2 of 2)
Description
T-cell lymphoma invasion and metastasis 2 [Source:HGNC Symbol;Acc:HGNC:11806]
Coordinates
chr20:4602688-4604875:+
Coord C1 exon
chr20:4602688-4602796
Coord A exon
chr20:4602900-4603079
Coord C2 exon
chr20:4604757-4604875
Length
180 bp
Sequences
Splice sites
3' ss Seq
ATTTCATTCTCTCATTGCAGCTA
3' ss Score
10.2
5' ss Seq
CAGGTGACC
5' ss Score
6.54
Exon sequences
Seq C1 exon
AAACTTCTCTTCTCCTTGGGCGGATCCTTCTTATACTATGCAGATCACTTCAAACTTTACAGCGGCTTCTGCGCCAATCACATTAAGGTGCAGAAAGTTCTGGAAAGAG
Seq A exon
CTAAAACAGACCGTGCATTCAAGGAGTTCCTGGAAGCGAGGAATCCCACAAAACAGCACTCGTCCACGCTGGAGTCGTACCTCATTAAACCTGTGCAGAGAGTCCTGAAGTATCCACTGCTGCTGAGGGAACTGGTGTCTCTCACTGACCCAGAGAGCGACCAGCACAACCACCTCACAG
Seq C2 exon
AAGCATTAAAGGCGATGGAGAAAGTGGCCAGTCACATCAACGAGATGCAGAAGATCTACGAGGACTACGGCACAGTGTTTGACCAGCTCGTGGCAGAGCAGAGCGGCCCGGAGAAGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000098233-'25-26,'25-25,26-26=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.066 C2=0.025
Domain overlap (PFAM):

C1:
PF0062115=RhoGEF=FE(18.9=100)
A:
PF0062115=RhoGEF=FE(31.6=100)
C2:
PF0062115=RhoGEF=PD(7.4=35.0)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TTCTCTTCTCCTTGGGCGGAT
R:
CTTCTCCGGGCCGCTCTG
Band lengths:
221-401
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]