Special

HsaEX1040765 @ hg38

Exon Skipping

Gene
Description
T-cell lymphoma invasion and metastasis 1 [Source:HGNC Symbol;Acc:HGNC:11805]
Coordinates
chr21:31130213-31154426:-
Coord C1 exon
chr21:31154247-31154426
Coord A exon
chr21:31146895-31147003
Coord C2 exon
chr21:31130213-31130315
Length
109 bp
Sequences
Splice sites
3' ss Seq
CCTTTTCTCGTCAAATCCAGAAA
3' ss Score
7.49
5' ss Seq
AAGGTAAGG
5' ss Score
10.51
Exon sequences
Seq C1 exon
AGTACAGAACAGGTGGCCGCATTTTGCCGCAGTTTGCATGAGATGAACCCCTCTGACCAGAGCCCATCTCCTCAGGACTCCACGGGGCCTCAGCTGGCGACCATGAGACAACTCTCGGATGCAGATAAGCTGCGCAAGGTGATCTGCGAGCTCCTGGAGACGGAGCGCACCTACGTGAAG
Seq A exon
AAAGTGCTGTTCTCTCTGGGGGGATCATTCCTGTATTATGCTGACCGCTTCAAGCTCTACAGTGCCTTCTGCGCCAGCCACACAAAAGTTCCCAAGGTCCTGGTGAAAG
Seq C2 exon
GTAGGATCTCACAGGCTTTCCATTTATGAGGACTGGGACCCCTTCAGATTTCGACACATGATCCCCACGGAAGCGCTGCAGGTTCGAGCTTTGGCGAGTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000156299_MULTIEX2-3/9=C1-8
Average complexity
C3
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.550 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
PF0062115=RhoGEF=PU(6.8=21.7)
A:
PF0062115=RhoGEF=FE(18.9=100)
C2:
PF0016924=PH=FE(25.6=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
AGAACAGGTGGCCGCATTTTG
R:
CTTCCGTGGGGATCATGTGTC
Band lengths:
248-357
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains