Special

HsaINT0167090 @ hg19

Intron Retention

Gene
Description
T-cell lymphoma invasion and metastasis 2 [Source:HGNC Symbol;Acc:11806]
Coordinates
chr6:155565145-155565917:+
Coord C1 exon
chr6:155565145-155565213
Coord A exon
chr6:155565214-155565791
Coord C2 exon
chr6:155565792-155565917
Length
578 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAAT
5' ss Score
8.39
3' ss Seq
AAATCCTGATCTTCACATAGATG
3' ss Score
4.5
Exon sequences
Seq C1 exon
GATTTGAGCTGCCTCTTTGAATTATACTTGGAGCCACTTCAGAATGAGACCTTTCTTACCCAAGATGAG
Seq A exon
GTAAATAAAATCACCTTCCTTCTGTCCAGTGATCCACAGGTTAGTCTCTGTTTGCCTTTTAGCAGAACTCCTATGAGAGTATCTCTGTTGATCCCAAAAGAACATCCCAAGACTTAACGGTCTTCTGAGAGTCCCAGGCATAGCCTCCTCCTAAACCACTGCTGTGGCCTCGGCTGCATGACCCAGTGGCAGAGTGTTTACAAAGGCAGAGGGACGGTTATGGTCTTTTTGAGGTAGAAGAGAGTGTGATCAGAAATTCCTTTTCAATACATACCTTTGTAATGTGAAACCACATAATTAGTTCTACTGACTTACATTTTTCTTAATTTGAATTCTGAGAATTTTACATCCACTTAAAAATTTACTGTAGTAATAGAGAATTATGGGGGATGGAGCTGTGAAACTTTCTATGTATAAGCCATATCCCATAATGAATGTGCTGTCTTCTTAAAGGATTTACTTTCTGTCTGCTTTTCCGTGAAGAATTTCCTTGTGATTTATTTGTGGGCCTAAGAGTTAGCGTGGTGTCCTGAACTTCATGGCTAATCCCCTCATTTCAAATCCTGATCTTCACATAG
Seq C2 exon
ATGGAGTCACTTTTTGGAAGTTTGCCAGAGATGCTTGAGTTTCAGAAGGTGTTTCTGGAGACCCTGGAGGATGGGATTTCAGCATCATCTGACTTTAACACCCTAGAAACCCCCTCACAGTTTAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000146426-TIAM2:NM_001010927:3
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0062115=RhoGEF=FE(11.6=100)
A:
NA
C2:
PF0062115=RhoGEF=FE(21.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Conservation
Rat
(rn6)
No conservation detected
Chicken
(galGal4)
Chicken
(galGal3)
ALTERNATIVE
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GATTTGAGCTGCCTCTTTGAAT
R:
ACTGTGAGGGGGTTTCTAGGG
Band lengths:
190-768
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]