Special

HsaINT1025937 @ hg38

Intron Retention

Gene
Description
NA
Coordinates
chr12:31135580-31136182:-
Coord C1 exon
chr12:31135954-31136182
Coord A exon
chr12:31135710-31135953
Coord C2 exon
chr12:31135580-31135709
Length
244 bp
Sequences
Splice sites
5' ss Seq
GAGGTGCGT
5' ss Score
8.42
3' ss Seq
TGCCATGATTGTTTTCTTAGATT
3' ss Score
7.22
Exon sequences
Seq C1 exon
TTCCTCAGGCTCTGCCAATCTTTCGTTCCTCATTCCTGATACGATAACCCAATGGGAGGCAAGTGGCTTTTGTGTGAATGGCGACGTTGGATTTGGCATTTCCTCTACAACCACTCTAGAAGTCTCCCAACCTTTCTTTATTGAAATTGCCTCACCCTTTTCGGTTGTTCAAAATGAACAATTTGATTTGATTGTCAATGCCTTCAGCTACCTGAATACATGTGTAGAG
Seq A exon
GTGCGTTGTTCTGTTTGATCTGGAGGCAAAAATCTAACAAAGCTAAAATATTCTTAATATTTCCATATTCTCTTTATCCTCAAGTGCAAAATGCTACTATAAAGGTATAAGACTTAGGTCCATATTCCTCAAACAAATACAATTGCTTTCATTCACAGTGACAGTTTAAACAGTGTATTGAGCATGGTGTTTCATAGTGATGTGTGTTCCAGTGCTATCCTCATTGCCATGATTGTTTTCTTAG
Seq C2 exon
ATTTCTGTTCAAGTGGAGGAGTCTCAGAATTATGAAGCAAATATTAATACCTGGAAAATCAATGGCAGTGAGGTTATTCAAGCTGGAGGGAGGAAAACAAACATCTGGACTATTATACCTAAGAAATTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000177359:ENST00000398963:17
Average complexity
IR
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:
PF0020717=A2M=FE(83.5=100)
A:
NA
C2:
PF0020717=A2M=PD(4.4=9.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
GCTCTGCCAATCTTTCGTTCC
R:
AGCTTGAATAACCTCACTGCCA
Band lengths:
305-549
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains