Special

GgaINT0102126 @ galGal4

Intron Retention

Gene
Description
villin-like [Source:HGNC Symbol;Acc:HGNC:30906]
Coordinates
chr2:4575589-4577455:+
Coord C1 exon
chr2:4575589-4575663
Coord A exon
chr2:4575664-4577258
Coord C2 exon
chr2:4577259-4577455
Length
1595 bp
Sequences
Splice sites
5' ss Seq
CACGTAAGT
5' ss Score
10.16
3' ss Seq
ATCTTTTCCACTTCTTCCAGAGC
3' ss Score
8.93
Exon sequences
Seq C1 exon
AACATGAAGATGGTTCCTGTACCTGAAAAAGCCTATGGGACTTTTTTTGAAGGGGACTGCTATGTAATTCTGCAC
Seq A exon
GTAAGTAAGGTGAACACAAACATTGGTCTCTTTGCAAGGATCAGCATCGTTTCTTGGGTTCCAACTTGATACTGGAGTGGTTGTGCACGTGCATTTGCCATCCAATCACACACCTGAATATAGTGTGGCTGTTGTAATGGCTCTGTGTGTCCAGTAAATCAGAAGTCCTGAGGAACCATTAGCAGTAACTCATTAAAATGATTTATCTTCTCACCCATTGATTTATGTCCAGATGTGGAAAAATGGCTGATATGTCCCCCAGAGTTAAGGCCGTTAAGGCCTGGATTTGCATGGCTTCTGGGAGTGTTTTTGGGATGGGAGAGGTGGCCAACTAGGAAATGTTATTTGCACAAGATGGTCACACCAACAGTGGAGAAGCTCTGCGGCCCTTCTCCCTCTCTCCCTTGGGAGACCTCTGCTGTCCCACCCAAATGTGGTCCAGACTTAATTGCAACCATTTGAACTCGGGCTAGGCAGAAGCACAGGTAAGTCCACCATGCACAGCCCATTATGGTATCTTCTGAGTGTTTTTGGAGAATCAGTTTGGCAGCAGCCACCCAAAGATGTGCTTAGAGCAGAATGTGAGTGTCCTTGCAGAGAGCTGGCTATAATCACTGTAGGTTTTGATGCTCACAGGCTCAGCTTATGTTGCAAGAGCTTCCCCAGGTAACAAAACCCTTAGTCAGTCTGCTGCTCTCCTTCCTCTCTGCAGATAAGTGGGTAAAAATATTCATCTTTGCATTCTGCACCTTAACTGGATGCTTTTCAAACAAAGCTTGTCGGCAGGACAATAGGACTTTGATCATCTTCAGTAACAGTGCATTAAATTGAACAATTTTGCCACAAATTAGTCAGCTGCGCCTAGAGGAATGGTGTTTTATTCAAGCTCTACTGTGTTTTTCGCTGTAGTATCACTGCACAAAGCAAATAAACAGAACTTAGTGTCAAATCGAGTTTATAAAATGAGCTTTTATTATCTTTTCCAGGCATGGATGATAGGACTTTAACACAGTAGGTGCTGAAAAATAACTGGCACGACTCACATAACGATAAGCACACCTGTTCTCAGATCACTTGCCTCTTCTTTCTGGGCTATTGGGTTTTTCTGTAATAAGATGAATCACAGCACGCACACGCGGGCTCAGCTTCATTTGGAGTTGTGTCTCTTTTGCAAGTCAGCAGGAACTCCCAGGCAGTTGGTGTTACTATGTGGTGTCATATGAGAAAGAGAAAGGGAGAGAAAGAATCTGATCTCCAGGCAAATAAGAGAGTATCTGGTACGTTTTTTTAAAGTGATCTATGAGAAGAATGTCCTTTAAGTTTTCATATCAAACTCTGCAAAAGTAGGACAGGTCAAACACATGAGGCTTTGGACTTCCACAGGTGCCTCGTTTTCCTTGATAACATGAGTCGTAAAAGCATATATAGTGGAAGCATGCTTCAGTGGAGCATCATTGGGCTCCATCCTATGGAGAGGGAGAAGGGGATGGGCCTTGGTAATGGGCTCCATGGTTACTTGTTTTGGCCAGTTCTCCCTGGACAGCAGCATTATGGCCTGTGTCTTCAACCTGTCTCATCTTTTCCACTTCTTCCAG
Seq C2 exon
AGCAAAAGAACCTCTCGTGGCACCGCTGTGGATTTGCATTACTGGATTGGGAAGGATTCATCCCAAGATGAGCAAGGTGCCGCGGCCATGTACGTCACCCAGCTGGACGCTGCGCTCAGGGGAAGCCCCGTGCAGCACCGGGAGGTGCAGGGACATGAGTCTGAGACCTTCCAAAGCTATTTCCGCAACGGCATCAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005763:ENSGALT00000009258:3
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=0.106
Domain overlap (PFAM):

C1:
PF0062617=Gelsolin=PU(28.9=96.0)
A:
NA
C2:
PF0062617=Gelsolin=PD(68.7=86.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACATGAAGATGGTTCCTGTACCTG
R:
CGTTGCGGAAATAGCTTTGGA
Band lengths:
264-1859
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]