Special

HsaINT0132962 @ hg19

Intron Retention

Gene
ENSG00000172382 | PRSS27
Description
protease, serine 27 [Source:HGNC Symbol;Acc:15475]
Coordinates
chr16:2762423-2763699:-
Coord C1 exon
chr16:2763530-2763699
Coord A exon
chr16:2762816-2763529
Coord C2 exon
chr16:2762423-2762815
Length
714 bp
Sequences
Splice sites
5' ss Seq
AAGGTGGGA
5' ss Score
6.03
3' ss Seq
TGACTCTGCGTCCCCCGCAGGGC
3' ss Score
11.23
Exon sequences
Seq C1 exon
ACCTCCTGCCCGAACCGCGGATCCTGCAGAAACTCGCTGTGCCCATCATCGACACACCCAAGTGCAACCTGCTCTACAGCAAAGACACCGAGTTTGGCTACCAACCCAAAACCATCAAGAATGACATGCTGTGCGCCGGCTTCGAGGAGGGCAAGAAGGATGCCTGCAAG
Seq A exon
GTGGGAGCAATGTGGTGTCCATGGGGACTCAGTCCCCACCGCCAGGCCCAGGGCAGGGTGGGATCATGCCCCGCTCCATGGGCTATGCATTCAACCAGCTGAGCAGCTTGTTTTGAAAAGGCAGATTCCAGGGCCGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGAGGGTGGATCACAAGGTCAGGAGATGGAGACCATCCTGGCTAACACAGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGCGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCAGTGCACTCCAGCCTGGGCCACAGAGCAAGACTCCGTCTCAATAAAAAAAAAAAAGAAAAAGCAGATTCCTGGACCCCACCCCAGAAGGATCAGAGTCAGTGGGTCTGGGGTGGGGCACAAGAAACTGCATTTTCAACACACACACACACCCTAGTTGATCTGGGGACACTAAAGAATAGGCACTTTAGACAATCGGACTGGCAGGGGATGGGGAGCCGGGCAGAGAGGCTCTGGGATGGAGAGAAGGAATCCATTGCGGAGCTACACACCTCCTGTGCGGCTGCAACTGAGTCTCTGGGAACTCAAGGTGGGCTCTGACGGTGACTCTGCGTCCCCCGCAG
Seq C2 exon
GGCGACTCGGGCGGCCCCCTGGTGTGCCTCGTGGGTCAGTCGTGGCTGCAGGCGGGGGTGATCAGCTGGGGTGAGGGCTGTGCCCGCCAGAACCGCCCAGGTGTCTACATCCGTGTCACCGCCCACCACAACTGGATCCATCGGATCATCCCCAAACTGCAGTTCCAGCCAGCGAGGTTGGGCGGCCAGAAGTGAGACCCCCGGGGCCAGGAGCCCCTTGAGCAGAGCTCTGCACCCAGCCTGCCCGCCCACACCATCCTGCTGGTCCTCCCAGCGCTGCTGTTGCACCTGTGAGCCCCACCAGACTCATTTGTAAATAGCGCTCCTTCCTCCCCTCTCAAATACCCTTATTTTATTTATGTTTCTCCCAATAAAAACCCAGCCTGTGTGCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000172382-PRSS27:NM_031948:5
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

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

C1:
PF0008921=Trypsin=FE(23.5=100)
A:
NA
C2:
PF0008921=Trypsin=PD(18.9=69.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTCGAGGAGGGCAAGAAGGAT
R:
CAAATGAGTCTGGTGGGGCTC
Band lengths:
343-1057
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development