Special

RnoINT0071166 @ rn6

Intron Retention

Gene
Description
hemicentin 1 [Source:RGD Symbol;Acc:1564772]
Coordinates
chr13:67979815-67981407:-
Coord C1 exon
chr13:67981326-67981407
Coord A exon
chr13:67979952-67981325
Coord C2 exon
chr13:67979815-67979951
Length
1374 bp
Sequences
Splice sites
5' ss Seq
ACGGTAACT
5' ss Score
7.53
3' ss Seq
TACGCTGTTCTCATGCTTAGTGC
3' ss Score
7.11
Exon sequences
Seq C1 exon
GTGGAGGACACAGGAAGATACACCTGCCTGGCATCCAGTCCTGCAGGGGACGATGATAAAGAATATCTAGTGAGAGTACACG
Seq A exon
GTAACTTTGGTGATTTATGTTGGAACCACATGCAATCCTAGTTAAAAACTGTACTAGAGAAGGTCCTGACATTTCACAGCACTTCATATGGAGATAAGTTGAGAAATGCATATTTTACAAATTTTATTCATTGTGTTAATAATGTATGAGCTCTTTGGGATATAGTTCATTGGAGTTTTGAGTTATTTGTCTTGTTTTCACCCAAACAATTCAAATTTGGTGACTTAAAAATAACAACATAAATTACAATAATGATTAGAATAAAAACAATCCATAGTCTTACCACACAAGGATACAATGTTTTTTTGTGTCTGTGAATATTTTATAGCTGAGCACAGCAGCATATATCTGTAGTCCCGGCTTCTTGGCAAGTTGAGGCAGGAAGATTGCTTAAGCTTAGGGAACTCATTAGGGAAATAAGAAGATCCTTACTATCAAAAAAAGGAACATTTCAGAACACAGAACTTAAGCCACTTTATGTCTCACTTAATGGCGTGATGAACACTCTTGTGTTAACACATATATTCCATAGCGTCATTTTAAGATTGCATGCTGCCATATATCTTACTCCCTTTTTAGAATTATTTAGACATATTAGGATAGTCTGCCTTTTTATCTATGTTGACAATATGTTAGCTATTTCCTTTATTTTTAAATTTTACTGTCCTACGCTGACTCGTTTCATATGCATGCATGTGCACATATGTCCTTTTAAAGATTTTTAAAATCATTGCCTTTTACTTTCCAGACAGTTTGAATTAACTAGGCCCTTTTGAATATTACTTTTATATATAAATTTAAATCACTCTTCATGGGGAGGAGTGTTTGAAAACCAAACAGAAATTGATCTAATTTTCAGTGCCTGACTGACTAGTCAATGCAGATCGTCTGGTATGAAGTTTCCCTGATATCCCTACTGAAAATTAAGGCCTACCTAAGTAAACCCAAATTATGATATACTGAGAAATATGTCTGTATTAATCAGGAAAAATGGACATTGTTCTTCATACTGCGATGGGCAGTTCCTTATTTGATCATTTTTCAGTAGTCAGAGTAAAGTATTACCCAGTGTGGAAGCTGATGGAAGGACAGCACTGTGCCTCTATTTCCTTACTACCCATCAAAGGTGACGATGGTGTAGTTATCTTATTATTCATGTGCTTTGCTGGAAAGATTCCATTATCTAATCAATAGGAAAGTGGTAAGTAATAAAGATCCAATTTGTTAATAATCTGGACCATACATTAGGTGACTAACCATTAAGGTCCATGCCTCCTTTATCGTCCCATAAACTTAGCCATTGTTGGAGACCAAATAGATCAATCATTTACAGCCCGTTTATCAAATGCACTGATACGCTGTTCTCATGCTTAG
Seq C2 exon
TGCCTCCTAACATTGCTGGAGTGGATGAAGCCCAGGACTTCACCGTGTTAAGGAACAGGCAGGTGACATTGGAATGCAAGTCCGACGCAGTGCCTCCACCTGTGATCATGTGGCTCAAAAATGGGGAGCAGTTACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000028627:ENSRNOT00000030971:71
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.214 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0767911=I-set=PD(29.1=89.3)
A:
NA
C2:
PF0767911=I-set=PU(44.7=82.6)


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:
GGACACAGGAAGATACACCTGC
R:
CTGTAACTGCTCCCCATTTTTGA
Band lengths:
214-1588
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]