Special

HsaINT0043007 @ hg19

Intron Retention

Gene
Description
chymotrypsinogen B2 [Source:HGNC Symbol;Acc:2522]
Coordinates
chr16:75237994-75238804:-
Coord C1 exon
chr16:75238671-75238804
Coord A exon
chr16:75238221-75238670
Coord C2 exon
chr16:75237994-75238220
Length
450 bp
Sequences
Splice sites
5' ss Seq
ATGGTGAGG
5' ss Score
7.61
3' ss Seq
ACTTCCTCTCCTTCCTGCAGGGT
3' ss Score
12.66
Exon sequences
Seq C1 exon
CCAACAAGACCCCTGACAAGCTGCAGCAGGCAGCCCTGCCCCTCCTGTCCAATGCCGAATGCAAGAAGTCCTGGGGCAGGAGGATCACCGACGTGATGATCTGTGCCGGGGCCAGTGGCGTCTCCTCCTGCATG
Seq A exon
GTGAGGCTGGCCCTGCCCAGGCCCTGGCCAGGCGAGCGGGGTGCAGGGGAGGTCTGGGCTTTCCACCCCTCTCTGCTCTCATCTACTAACCCCACACCCTCCTGGGGCCCAGTGAGGGCCAGGCCTTGGGGTCACAGCCGCCCATGAGGGTTCCTCCAGGCCATGCAGCTGAGGCTGCCCCTGGGGACTTCCTTGCAGCCCTGTGAGCTGGAGGTTTGGAGAGATGGATGGTGCCCCGGCTTAGAGAGGGAAGCCACCTGCCCCAGCTCCCTCCAAGAGTGCATGGCAGAGTGGGGGCTGCCATGTGAACCCAGATCTCAGGACCCCGGCACAGCCCCTATGCCCATGCTTACCATTTCTCCGCACCCCTCCCTAGACTCCACCAGGTCAGGGTCCCCTAGGCCCTGGCACCCCTTTCAGGCCTAGAGATACTTCCTCTCCTTCCTGCAG
Seq C2 exon
GGTGACTCTGGAGGCCCCCTGGTCTGCCAGAAGGACGGAGCCTGGACCCTGGTGGGCATTGTGTCCTGGGGCAGCCGCACCTGCTCTACCACCACGCCCGCTGTGTACGCCCGTGTCGCCAAGCTCATACCCTGGGTGCAGAAGATCCTGGCCGCCAACTGAGCCCGCAGCTCCTGCCACCCCTGCCTTAAGATTTCCCATTAAATGCATCTGTTTAGAAGCCCTGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000168928-CTRB2:NM_001025200:6
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

No protein impact description available

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

C1:
PF0008921=Trypsin=FE(19.7=100)
A:
NA
C2:
PF0008921=Trypsin=PD(20.2=83.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Rat
(rn6)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AACAAGACCCCTGACAAGCTG
R:
CAGGGCTTCTAAACAGATGCA
Band lengths:
358-808
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]