Special

RnoINT0156977 @ rn6

Intron Retention

Gene
Description
TSC complex subunit 1 [Source:RGD Symbol;Acc:620124]
Coordinates
chr3:7238977-7239890:+
Coord C1 exon
chr3:7238977-7239080
Coord A exon
chr3:7239081-7239737
Coord C2 exon
chr3:7239738-7239890
Length
657 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGT
5' ss Score
10.47
3' ss Seq
TTGATGTTTTATATTTTCAGCAC
3' ss Score
7.77
Exon sequences
Seq C1 exon
AACGTGGGCCTATGCTTGTAAACACGTTGGTGGATTATTACCTGGAAACCAATTCTCAGCCGGTCTTGCACATCCTGACCACCCTGCAAGAGCCACATGATAAG
Seq A exon
GTGAGTGCTGGTGGGATAGCATGGCAGTCCGTATATCCTCAGCCAAGCGAGGGTGGGTGTGAGCCGCAACAGCTCCTCCATAGGTTGGAAAATCGACATGGAAAATCTGAACATCGACAAAATAGCACTGATTTCAGAGGCTTTTTACAGATCTTGCTCTTTAAAGAAATCTTATAATTCTAGTACTAGAGTAAATTAATGACAGTTGAAATAAAGATCTTTAAACCTGTGCTGTGAGTCGGGTTTTTGGATTTACCAAGCAGGGGAAAGCCCTGGTGCAGCCCTCTACGTCTGCATGTGCTGGTGAAGTTGTTCACCCAGGGCTGCATGCTCTTCTTTATTCTGGGCTGAGTGCAGCAGCATAGCGCCTGCCTTCTAGCTGAGGCTAGAGCGTATGTGCTTGGCTGTTACAGTCGTTAGGGATCCTTTTTCTTACACTGCAGCTGTTCTCTCAGGCCACAGGAAGAAAACTTTGTTCACTAGTGTGGTTCTGAAATCCTGGATTGAACAAGCCCTAGCCTTTACAGGGCAGGTGCATCGCCAGCCCATCTTTTGGTGCTTGTGTTAGAGGAAGTCTTGAGACCTTGGAGTTTATCAGTTTATTGGTAAACTTCATATGCTTCCCGGAAATTTTCTCTTGATGTTTTATATTTTCAG
Seq C2 exon
CACCTCTTGGACAAAATGAATGAGTATGTAGGCAAAGCTGCCACCCGCTTATCCATCCTCTCGCTGCTGGGGCATGTTGTGAGGCTGCAGCCATCTTGGAAGCATAAGCTCTCTCAAGCACCTCTTCTGCCTTCTTTACTGAAATGTCTCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000011470:ENSRNOT00000016904:2
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:
PF043887=Hamartin=FE(4.7=100)
A:
NA
C2:
PF043887=Hamartin=FE(7.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACGTGGGCCTATGCTTGTAAA
R:
TGAGACATTTCAGTAAAGAAGGCAGA
Band lengths:
254-911
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]