Special

RnoINT0071185 @ rn6

Intron Retention

Gene
Description
hemicentin 1 [Source:RGD Symbol;Acc:1564772]
Coordinates
chr13:67949849-67950322:-
Coord C1 exon
chr13:67950152-67950322
Coord A exon
chr13:67950020-67950151
Coord C2 exon
chr13:67949849-67950019
Length
132 bp
Sequences
Splice sites
5' ss Seq
CAGGTATGT
5' ss Score
9.8
3' ss Seq
ATGGTTTTACCTCCCTGTAGTGG
3' ss Score
6.6
Exon sequences
Seq C1 exon
TGCATGGTGGGTTTTCGTTGTGGTCTGCCTGGAGGTCCTGCAGTGTCACCTGTGGAAAAGGCATCCAAAAGAGGAGCAGGCTATGCAACAACCCTCCTCCAGCCAATGGAGGGAGGCCATGCCAAGGCTCAGAGTCAGAAGCACGACAGTGTCAAAATAAGTTGTGTCCAG
Seq A exon
GTATGTCTCTGCATTCAGTGAATAGGCATGTGTTTAATAGACACTAATTTATGTTCCTACCTTTGGCTGCCTCGTGGTCACTACTTGCCATTCGACTTTAGCTAATGATGTAATGGTTTTACCTCCCTGTAG
Seq C2 exon
TGGATGGTCACTGGTCAGAATGGAGCTTCTGGGAAGAATGCTCAAGAAGCTGTGGGCATGGCAACCAAACTAGGACGAGAACTTGCAGTAACCCACCGGCTCAGCATGGTGGGCGGCCATGTGAGGGGTATGCTGTGGAAACCATCATGTGTAACATTCGGCCTTGCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000028627:ENSRNOT00000030971:89
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.103 A=NA C2=0.034
Domain overlap (PFAM):

C1:
PF0009014=TSP_1=WD(100=87.9)
A:
NA
C2:
PF0009014=TSP_1=WD(100=87.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCATGGTGGGTTTTCGTTGTG
R:
TCCTAGTTTGGTTGCCATGCC
Band lengths:
245-377
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]