HsaINT0129573 @ hg19
Intron Retention
Gene
ENSG00000130714 | POMT1
Description
protein-O-mannosyltransferase 1 [Source:HGNC Symbol;Acc:9202]
Coordinates
chr9:134395467-134396859:+
Coord C1 exon
chr9:134395467-134395580
Coord A exon
chr9:134395581-134396732
Coord C2 exon
chr9:134396733-134396859
Length
1152 bp
Sequences
Splice sites
5' ss Seq
AGCGTAAGC
5' ss Score
6.06
3' ss Seq
CATCTCCCATGTTCCCTTAGGCT
3' ss Score
10.57
Exon sequences
Seq C1 exon
TGGAGGATGCTGGCGCTGAGAAGTGATGACTCGGAACACAAGTACAGCTCCAGCCCACTGGAGTGGGTCACCCTGGACACCAATATTGCCTACTGGCTGCACCCCAGGACCAGC
Seq A exon
GTAAGCGAGCGATGCTGACAGCTGACAGTCATAGATTCATCCTGTTTCTTGAGAATTCCTTGCATTAAGAGCAGCCGCTGCACCCTAGAAAGTGCTGGGTTTCTCCCAAGCTTTTCCTGACAAAGGCCTGTGACTTGGTTTTCTCTAAACGCTTTGGCAACCTGGAGCCAGGAGTAGGGGTGTGGCATGTGTGCCTGTTGAAGGAAACCCGGCTTGATTGCTTTTGTGGAGACACATTGTTCCCCTTTTCCTGGCGAAAGTGGTTTTAAGATATTCCCATTCAATTTTCCGTGTGGCACCTGGTGGTGGAGCTTACCGGTGCTTTGCTGATGTGCGTGCCGTCTCTCCACCCGGCAGAGTGAAAGCATTGGTAGGCCGGGCGCACAGTCAGCGCCCCATAAATATTCACTGAATGGGCAGACGCTGGAAATGCCCACCTTTTTCCTCCTCCCTCAGAGGCGGGTAGGTCGGCTCAGCATGTGCACTGAAGGCAGAGGCTCAGGCCCAGAGGCCGCCCCACCCCGAGCTCTGAGCGCACTTTGCATTCTCCTCCGTGGACAGCGCTGCTGTTACAAAGTGGAGTCATCTGCTCCCAATTTTCAGTTTCCAATTACAAAATTGAGAGCATCAGTGCTGTGTGTGTGTGTGTATGTGAGAGAGAAAGAGAGAGACGGAGTCTTGCTCTGTCATCCAGGCTGGAGTACAGTGGCGTGATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCAAGTAGCTGGTATTACAGGTGCCCACCGCAATGCCCAGCTAATTTTTGTACTTTTTAATAGAGACGGGGTTTCGCCACGTTGGGCAGGCTGGTCTCAAACTCCTGACTTCAGGTGATCTGCCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGCATGTGCCACCACACCCGGCTGGCATCAGTGCTTTTAATGAAAGGTCTGAGTAGGAGCAGACCTGTCCACAGTAGTAGTAAGGCCTAGTGGATGCTAGGCTGTGCCTGGCGTTTTTTCACTCTGCTAAAGTAGTGCGTGCATCTGAATTCCTTTCCTGTGTTCTCTTCTCTTCCCTCCCTGAGCAGAGGGCAGGTGGCTAACAGCATCTCCCATGTTCCCTTAG
Seq C2 exon
GCTCAGATCCACCTACTTGGAAACATAGTGATCTGGGTTTCGGGCAGCCTCGCTCTGGCCATCTACGCCCTGCTGTCCTTGTGGTACCTGCTCCGACGGCGAAGAAATGTCCATGACCTCCCTCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000130714-POMT1:NM_007171:17
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:
NO
A:
NA
C2:
NO
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GAGGATGCTGGCGCTGAGAA
R:
CCTGAGGGAGGTCATGGACAT
Band lengths:
239-1391
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)