Special

DreINT0022387 @ danRer10

Intron Retention

Gene
Description
villin-like [Source:HGNC Symbol;Acc:HGNC:30906]
Coordinates
chr24:20288206-20290753:-
Coord C1 exon
chr24:20290548-20290753
Coord A exon
chr24:20288285-20290547
Coord C2 exon
chr24:20288206-20288284
Length
2263 bp
Sequences
Splice sites
5' ss Seq
CCAGTATGA
5' ss Score
2.36
3' ss Seq
TTGCTTGGGTTTTTTCACAGGGT
3' ss Score
8.05
Exon sequences
Seq C1 exon
GCTGTTATGTTGGCTCAGGACATCAGGGACCGAGAGAGAGGAGGACGGGCTCAGATTGGCGTGATTGAGGGTGCACAGGAGGAAGCTTCTCCTGAGCTAATGAAGGTCATGGTCTCGGTTTTGGGTCAGAGGATTGGTCAAATGAAAGAGGCAATACCTGATGACAAACCAGGCCAAAACCAGATCTCCAATGTCAAACTCTACCA
Seq A exon
GTATGAACACTTTCATCAGTCTTTCTAACTGTAAAGTTTATGTCATATAAAAATGCAGAAAAACACAAACTTAAAAAAAGCAAAACAGCCTTCCTGAAGGGTTTAAACACTAAACAACAAAAAAATTGTATCGTACAAACAGTCCCAGACCTTGAGCTGGTCTCAAAAAGGGACTAAACAAGGACAGACAGATACAAACAGGTGTTAATCGGCTAGCAGCTAGTTCTCTGCAGCTCCCACTGAAGTTAAACAGAGTTGTACCTGGTAAGTACATGAATTGTAGAACACATGTGAAAGTCAGATGAGGCCTTAGATTCAACCCAGGCTCATTCTAGAACCATACCTCTATATACATTTCTGGAGAGCACCAAATGCGTCCCAGGAGCTACGTATTTTTTGCAGTTTTTGTTTTCGCGAATCCACTTGTGTATGCTTTTTGAGATCTCAAATTTCTCTCGCGAGTGCCATTCGCCGCTGCTGTTCCATGTAAATCCACCAGAGGTCGTTGTTGACTGACTGAATGACTGACTGACTGACCGATTGATTAAACCACCCTCCTCCTTCCCTAAACCCAAGCAATAGTGTTATTAAAAGCAACGATTGAACCGGCTCAAGTCCCCCGACGTACATGGTAATCTACAGAACAAACTTGTAACAGCGAGAAAGCCTCAGCTGGTAAGCGCGAAAAGGAACAGTGTCATACTGCCCCATGTCATTGGTTTTAAAGAAGAAATGCAGCCATATGTAATTCTGGCTTCATATTATCTCTTATCTCATACTTATCTCTTTTGCTTGTTTGCTTATTTTTAATTGTTATTGTGTCTGAACTTGCTAAAGTGCTCTGTGAGTCCAAAGAAAATTTCCCCTTGAGGAAAAATAAAGTATACAAATGAACAAACAAACATAATTTGCAATTTCCAGAAACGTCTACAGGGCTACATTTTCAGGATGAGCCTATGTTGCTTAGATTATAGTGCCACGATATATCAACAGGGACACTGTACTCTCGGTGAGAGTTGTCCTTCAGATGAGATATTAAACCATAGTCCTGACTCTCTGTTGTCATTTAAAATACAAGGATTTCTTTCAAACAAAGCAGCATTGTGTTCCTGGCATCCTTGCCAAACTTGCACACTTGCCTCTGTCCATCATGGCCTCCTAACTATCACCATACCATCAAATTGGCTTCATCACATCACAGTCCCACCCTTTGAGTGCCCAGAAAAGCATTATATAAATGTAATGAATTATTATGAATAATTATATAATGAATTGCCATTACAAATAAGGAACAAACTTGAATATGGAGCAAAGAAAACAAAATCCTTAAACCAAAGCTAAGCTGACATCTGGGAAGACCTGACTTCAAGCTGTAACTGATAAATTGTGGGGTTGATGGTGAAGGTTCCGATGGCAGAATAGGGGTTGAGGGAAACAGATGGTATGCCATGAATGAACTGAGGAAGGAATTCTGAAGGAGCTTGTGGTGGGATGATCCATGATAGAATTTTAAGGCCAGCTGACAGACGTGATATAACAGACAGAGGTTCCTGATGGGCTGAGAAATGAGGTGCCACAGAAGGACCAAAAGATCAAGACTGAGATACGACAAGCAGCTGCTGTAGAGTTGATGATGGTGTGAGTGAGGATAGAGGTGGAGGTAAGGAGGAGCATGCTGGAGGTGGAGGAATGAAGTACTGTCAAAAGTCCAGAAGTTCATGGCAAAGGTACAGCTGTGACTGGCCAAGATGGAGCTGGAAGGATGTTGCCCCCTAGTGGAACTGATGGGATGAGGAGGCTGGACAGTGTCAGTTGGTTGATGAGCTGAGGTTGAATTGAGGTTACCGAAAGATGAGGCAGAAACAGAGAATCAGTACACTATGACAAAGCTAGAGAATGGAAGCCCCATGGCAGAGCCAATAGAAGAGCCAACAAGAGTGAAAAAACTGGGTATGAACCTAAAACACAGAGCATGTGCTGCATGAGGAAACAAACAACTCAAGAACAGGTGAAGAACAAATGAAGAACAGGTAGTGCTGGATGGGACCAGAAGCAATGAATCTCTTCCATTTCACTTGCTATTTCCATTTCCTAGTCAATCAAACAGGGCTCTTCTCATCCAGCTCAATGATTGATTGTGTAAATAGCTAGCATTGAAGCATTAGCAACATCCTTGTTGTTGATAACAACTGCTGATAATTACTTGATAATTTAGTGCTAACATTAAACAAAATAACTTTAATTTGCTTGGGTTTTTTCACAG
Seq C2 exon
GGTGTCAGACGCCAGTGGTCAGCTGTTGGTACAGGAAGTGGCTGTCAGTCCACTCACCCAGGATCTGCTGTGCTCCTCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000001909:ENSDART00000048940:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.203 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0062617=Gelsolin=PD(40.5=43.5)
A:
NA
C2:
PF0062617=Gelsolin=PU(20.8=59.3)


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:
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]