Special

GgaINT0039721 @ galGal4

Intron Retention

Description
tenascin N [Source:HGNC Symbol;Acc:HGNC:22942]
Coordinates
chr8:7061619-7062922:-
Coord C1 exon
chr8:7062659-7062922
Coord A exon
chr8:7061883-7062658
Coord C2 exon
chr8:7061619-7061882
Length
776 bp
Sequences
Splice sites
5' ss Seq
CAGGTATTC
5' ss Score
6.49
3' ss Seq
CTTTACACTTTATTTCTTAGAAT
3' ss Score
8.6
Exon sequences
Seq C1 exon
AAATTGACAGCCCCACTCACCTGGTGACTGATCAAGTGACAGAGGACACAGTCACCATCTCCTGGGACAGGGTTCTGGCTCTCATAGATAGGTACATGGTGAATTACACCTCTGCCAATGGTGATACTGAGGAGATAGAAGTGGCGAAGAACAAGACTGCCACAACTCTGGTAGGACTGAAACCTGGCACTGAATATGTCATCTACCTCTGGGCAGAGAAAGGAGTGCGGCAGAGCAAGAGGACCAGCACTGAAGCAGTGACAG
Seq A exon
GTATTCCAGAACAATTCTTGTGGTTCTACCCTATGTTGTGAAGGTGATCTGTTTCTACCCTGTCTGCTTCCTTCTGTTTCAGTGTGTACTAGACAGCAATTTATCTTGTGCCCACCTATGATGTGGAAACATTCATATTACAGACACTTCAAGCTTCAGGTAGAAATACTGCCTCCTCTCAAGTCAGGAGAAAAGATGTTAATTAATTCTAGGAACTAACAACTGATCTGTGAATTTAGAAACTATCAGACCAGTGTGAGCTTCATTATGCTTTGCCAAAGCACTGTAGCCCTCACTTACCACACCAGCCATACATGCTGGTTTTGATCTCGAGGTATGCTGAGCTCTGCAGGTGTGGCTGAGTGCCATTCCACAGTATATAATACTGCTGTTGAATCCTACTTACAATTATGTGCCACTGATAAGAATGGCATTAGCCAACGATTCAAGGCCTGGAAGGAAACACTCCCACTTTATTCATCTTCCATAACCCAAAAGGGTGAAGAATTTTTTGAGCCCAGAACCAGTATCAGTTCACTTCATATCGTGGAGGCCTTTGCTTGCAGCATCTGGATGCTTAGTTAAGCTGAAAACTGACTCACTGGCAGCTTCCTAAAAATGAGGAAAAGATAGAGAAGATGAGAGGTCTCACTATCCTGATTAGCTTGAAGGCAGACACTGTGTACATCATCTGTGTCATGGGGCTATAGAAAGCTAAAGCTTTTAAGAGAAGCGTGTGTGTTTTAGTTACTTATACTTTACACTTTATTTCTTAG
Seq C2 exon
AATTGGACAGCCCAAAGAATCTGGTAACCGACCAAGTGACAGAAGACTCAGCCACGATCTCCTGGGATAGCGTCCGAGCTCCCATAGATAGGTACATTGTGAGCTACACTTCTGCTGATGGGGGCAGCAAGGAAATAGAAGTGGGGAAGGCCAAGAGCGTTACAACTCTGACAGGACTGAAAGCAGGCATGAAGTACACCATCCATCTCTGGGCAGAGCTGGGAAGCATGCAGAGCAAGAAGGCAAGCACTGATGCGCTGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000004538:ENSGALT00000043017:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.287 A=NA C2=0.213
Domain overlap (PFAM):

C1:
PF0004116=fn3=WD(100=89.9)
A:
NA
C2:
PF0004116=fn3=WD(100=86.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGGTAGGACTGAAACCTGGCA
R:
TCAGTGCTTGCCTTCTTGCTC
Band lengths:
349-1125
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]