Special

HsaINT0126521 @ hg19

Intron Retention

Gene
Description
plasminogen activator, tissue [Source:HGNC Symbol;Acc:9051]
Coordinates
chr8:42044916-42045534:-
Coord C1 exon
chr8:42045424-42045534
Coord A exon
chr8:42045091-42045423
Coord C2 exon
chr8:42044916-42045090
Length
333 bp
Sequences
Splice sites
5' ss Seq
TAGGTGAGT
5' ss Score
8.83
3' ss Seq
CATGCCCTGCTCTCTGTCAGATA
3' ss Score
8.7
Exon sequences
Seq C1 exon
GTTGCAGCGAGCCAAGGTGTTTCAACGGGGGCACCTGCCAGCAGGCCCTGTACTTCTCAGATTTCGTGTGCCAGTGCCCCGAAGGATTTGCTGGGAAGTGCTGTGAAATAG
Seq A exon
GTGAGTAGGTGAGAGCACGTGAAACGAGCTGAAATCCCACCTCTCCAGTCTCCCCCGCCCCCGGAAGGAAAGGCAGGGTGCGATGGCAGGGCCAGGGGTGGGGGCCAGGGACAGGGAAGGCGCTTCTGCCATGGGTCAGGAAGCACAGTGCCACACAGCAAGCAGAGCCTAGGTGTGACCCTGAATCCAGGCTGGCACCCTTGCCACCCAGCCTGTGGCTTCCGAGCCAGCCTGCATCAGGCCTGGGGGAGGACGGGGCAGAGAGGGGAGCCTCCTGAGGGCTGAATGAAAGGGGACTCCCATGTGAGGCATCCATGCCCTGCTCTCTGTCAG
Seq C2 exon
ATACCAGGGCCACGTGCTACGAGGACCAGGGCATCAGCTACAGGGGCACGTGGAGCACAGCGGAGAGTGGCGCCGAGTGCACCAACTGGAACAGCAGCGCGTTGGCCCAGAAGCCCTACAGCGGGCGGAGGCCAGACGCCATCAGGCTGGGCCTGGGGAACCACAACTACTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000104368-PLAT:NM_033011:4
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:
PF0000822=EGF=WD(100=84.2)
A:
NA
C2:
PF0005113=Kringle=PU(64.6=89.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Zebrafish
(danRer10)
LOW PSI
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GTTGCAGCGAGCCAAGGT
R:
CTGCAGTAGTTGTGGTTCCCC
Band lengths:
286-619
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