Special

GgaINT0069295 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr4:82880307-82881722:+
Coord C1 exon
chr4:82880307-82880387
Coord A exon
chr4:82880388-82881627
Coord C2 exon
chr4:82881628-82881722
Length
1240 bp
Sequences
Splice sites
5' ss Seq
AAGGTATGT
5' ss Score
9.79
3' ss Seq
AGTAACTTTGGCTTTTGTAGATG
3' ss Score
6.27
Exon sequences
Seq C1 exon
AGCTATACGATATTTGTCTGGCTCGTGCCAAAGAAAAATGGCGATCACGTAGCACGGTAGGAGCTGAGGTAGAATGTGAAG
Seq A exon
GTATGTTTTCTTTTGGTGAATAACTTACAGTGTGCTACAGAATATATAGAATATATTCTGTATGTGTGTATATATATATATAAATATATAGAATATATATACAGAATATAAAGATGAAATTGATTTAAAAAAAACAAGCAAAAAAACCTTTGTTGTGGAAGAAACAGGTGCATTCTTCTTAATTAATCTTTTGTCTCTTATATACCATGCTTGTTCAGTTTTTTTTTTGAAATCTTTCTCTAGGTACAGTTATGAATTGATACCTAATTTGTAGGAAAACTAGGAACGTTTGGGAGGTTCTAATTTGGACTGAAGCACAAATATTTTGCTGCCTCTGCAGTTTTGTAATTGAAACTCAAATCATAGCAGAAAGTTAAATTTTAGTTCCTTAGTGCAGCTTTAGGTCCATCTCTTGGGCATGTTTCAGAGAGAAGCAATTTATTTTTGCATATGAAGTGGTTTGAGATTTACTAATTGATTAGAGGAGTTGTATTTTTGAAAGTATTACGTTGCTGCTTGAAGTTTGTCTTTGATAAATAATTACACTGAGCAGAAAAAGGAGAACATATGTACTGCTGGTGTTTATCCACAGAAAAGTATGGTTAGTTGGAAACCCCCAACTTTGTTTTCTTAAGATGCAATTTCCTGCATCTTAATTGTGATGACATTGGGTGCATTTCCAGCTTTCTCTTGCATTTTATTTTCTGGAATACGTATCTTCGTATGGTTGTTATAAATTACTGCTTTTTGCTAGTGACAAGTCTTATTTTTTCATTACTCCAGAAGTGGTAATGGCTAGTTCCCAACTATATTTAACCAGGACAAGTGAAATAGAACTGAAGTTTTTGGGTCTCGCATACTTTAGAAACTGACTTTCAGTGAGGTCTGCTTCAGTTTTGGACCATGATCTTTAACAGAGCATACGAAGAGTGAATATGATTCTGGAATGTGAGCCAACAGTAGTAGACATTGATGACATGCAGTCTATAATTCTTTAGATCTTCTCTCACCAGAACCTCTCTACGGAGGTGACTACTTAAAGAGCTATTGGAAGCCCTGTTTGAAAGCCAACAGGCTTGTGTGCGTCCATTGGTTTGTCAAAAAATGCCAATGAAATTCCTGGCTTGTTTTGCCTTGCCTCCTTCTCTTTCTCTCTACCCTCATGACTTCATAACAGTTGTGGGGGGGAAAAGGTGTACACTGATCCATGTAATAAGAGCAGTAACTTTGGCTTTTGTAG
Seq C2 exon
ATGCTGGATTTTCTACAGCTGACAGAGAAGCAAGTTTGGAGTTAATAAAACTGGATATCTCAAGAACGTTTCCTAATCTCTGTATATTCCAACAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000015546:ENSGALT00000025058:7
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=0.000
Domain overlap (PFAM):

C1:
PF0056613=RabGAP-TBC=FE(11.8=100)
A:
NA
C2:
PF0056613=RabGAP-TBC=FE(13.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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]