Special

RnoINT0040029 @ rn6

Intron Retention

Gene
Description
collagen type V alpha 2 chain [Source:RGD Symbol;Acc:70921]
Coordinates
chr9:52121315-52122748:-
Coord C1 exon
chr9:52122734-52122748
Coord A exon
chr9:52121369-52122733
Coord C2 exon
chr9:52121315-52121368
Length
1365 bp
Sequences
Splice sites
5' ss Seq
AGGGTAAAT
5' ss Score
5.83
3' ss Seq
GCATTTTTGGTCCATTGTAGGGT
3' ss Score
9.3
Exon sequences
Seq C1 exon
CCAATGGGAGAAAGG
Seq A exon
GTAAATATGAATAATAAAATTATTGTTTGTCTCCTCTCCTGAACATGTGTTTTTGAAAGTTGCATGAGTAAAATTGTGAGTAGAAAGGAAACAGAAAGCAAGAAAGAGATGGTGCAGATGCCTCGCAGAGCATAGTGTTTATCTTGATGTAAAAAGAGCCAAATGTTTATTTAAGCTTCACTCATTGATTCAACAAATATCGTCTGACTGATTAGTGTAAGCCAGCTCTACATTGAGTGTTTGGGATATATCAGTGGACAAGAAACTTGTGGTCCTAATCCTCATCTGGGTTGTAGTGGATGGACTTAGTGGGTAGCAAACAGTGAAACACATTGTAGTAAGTGCCCTATACAGTTTTAATTGGTGATAGTGGGGACTAATGATGGGTAGAGATCAGTGACAGCTGCTATATTAGGTGGTAGGAGACACAGGAGTATGAGAAGATAGCAAGTAGGTTGAATCTGGAGGAGAAAAAACCTGCTAGGGAACATGTCAGACAGAACACTCAGTTCTCATCAGAGAAGCAAGAGAGAACTTGGCAGGTTTTCTTTGTTTGTTTGTTTGTTTGTTTTTTGTTTTTTGTTGTTGTTGTTGTTGTTGTTGCTGCTGTTGCTGTTGTTGTTGTTTTTATTTTTGTTTTTTATTGGATATTTTTTTATTTACCTTTCAAATGTTATTCCCTTTCCCAGTTTCCCATTCATAAGCTCCCTATCCCATCCTCTCCCCTTCTGCTATAAGGGTGTTCCCCTTCCCCAAACACCTCCTCTTCCTGCCTCCCCTCCCTGATATTCCCCTGTACTGGGGGGTCCAGCCTTGGTAGGACCAAGGACTTCTCCTCCCATTGGTGCCCAGCAAGGCCTTCCTCTTCTACATATGCAGCTGGAGCCATGGGTCTGTCCATGTGTATTCTTTGGGTAGTGGTTTAGTCCCTGGTTGGCAGTTTTAAAGAATAGAAGAGGGTGGGTCAGTGGGGTACAAGAAAATGGACATGAAGAAACAATGCTGATTTCAATTTGTATAGTTTTAGTATAAGCCAAAGTCTACAAGATGACAGAAAATTCTCTACTGATGACACTTTGATCACTATAATCAGTAACTGTGCTTCTTGTTTCTATATATTAGATTTTTTTGTATTTATTTTACAATTAATTTTTAGAGGGTTTCTTTTGAAAGGTTTGGTTTACTACTCATGTTTGTCAAAATTTCAAGTAATTTTTCTAGTAAGATTATTTTCTTTGTATTTTTATTCTGCTGTGTTAACTTGGTCAGAGCTCTGAAAATCTAATAATACCTGAAATAAATCCTTTTACTAGGTACATGTGCCAATGATAAATATCTCAAAACTGCATTTTTGGTCCATTGTAG
Seq C2 exon
GGTGCTCCTGGCAATCGTGGTTTTCCAGGTTCTGATGGTTTACCTGGACCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000003736:ENSRNOT00000005073:24
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=1.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]