Special

GgaINT0038832 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr8:6774594-6777572:-
Coord C1 exon
chr8:6777018-6777572
Coord A exon
chr8:6774739-6777017
Coord C2 exon
chr8:6774594-6774738
Length
2279 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGA
5' ss Score
10.57
3' ss Seq
CATCTGACCTTTTCCTTCAGGAC
3' ss Score
10.7
Exon sequences
Seq C1 exon
GACAACTGCCGTCGAGCTGAAAATGTGCTCCGTCTCTGGATCATTGAGGCAAAGGACCTGGCCCCCAAGAAGAAATACTTCTGTGAGCTGTGCCTTGATGACACTCTCTTTGCCCGCACCACCAGCAAAACGAAAGCAGATAACATTTTCTGGGGGGAGCACTTTGAGTTCTACGGCCTCCCAGCTCTTCACAGCATCACGGTTCACATCTACAAGGATGTGGAGAAGAAAAAGAAAAAGGACAAAAACAATTACGTCGGCCTGGTCAACATTCCCATGGCCACTGTAACGGGGCGCCAGTTTGTGGAAAAATGGTACCCAGTCAGCACACCTACACCCAACAAAGGGAAATCAGGAGGCCCTTCCATTCGCATCAAGTCGCGTTATCAGACCATCACCATCTTACCCATGGAGCAATACAAGGAGTTTGCAGAGTTTGTTACCAGCAACTACACGATGCTGTGCTCTGTGCTGGAGCCAGTCATCAGCGTAAGGAATAAGGAAGAGATGGCTTGTGCAATGGTGCACATTCTTCAGAGCACGGGGAGAGCCAAG
Seq A exon
GTAAGAGTGGGCGGCCCCTGCCAAAATGGCTCCTTCCTCCTGATGATAGGTGATACCTTCTCAACTATTAGCCTGTAGAAAATAGGCTTCCTGGGCTGGTGTGACCGCAAGCAGCCACACAAGGTGCCCGATGGGCTAAGGCTGAGAAGAGGGCCTCAAAAGTGTTTCTAAAGACTTGGCGATTACATCCACCAGGAAGGCATGCAAATAGGTACCACACCAACACAAATTAAGTGCCTGAGTTGATAGGAAGGTTAAAGATACTGTGTACAGAGCGTAAGTGGGAGGACTGAAAAATGAGAGCCTGCACTCTAAGTATTCAGGAACCTTTTCTGTGTTTCTAGAATTGTGATACTAAATAAAGAGATAAGTAAGCAAGAGTTAAATAGACCAGAGAATAACTTCTATAAATACATCTCCAATACAGTGAGCAGCAGCATGTTGATTCAGTGCTAAGTCAGCTAATCGACGTGAACATTGATTTGGTCAGCAATTGAACAGCCATTTGGAGAATCCAGGCTCAGTTAATGGTGATCCCACCTGCCCCAAGAACGGTATTAGGACTTCCAGGTGCACGCTGGTGGTTCTCTGTAATGCAGTAATTGATGTGAGCCCTGGTTTCTTTGAACAGATTGTGGGAGAATATCCTGCAGGATTCCAGAAATTCTGAGAAGCATTAACAAGCATTGATTGATCCAGGTGCTGCCTGCCAAGTGGCTGTATGGGAGTAGTACCAAGCTGTAGCCAGCTCCTTCCAGTAATGCCAGCTAGAGCAAGTTAAGCACCACTGAGCACAGGCTGGAGTTGGAGGTGTGAGACAATGACCACAAGCAGCAGTCAAGGGACAGCTTAAAAATTAACTGCTCTGAAAAGATCCCATTGTAACTCTCAAGAGTTACCACTCTCTGCTGTTCCCTGTTGCTTGATGTAGAGCTCAGGAAGGCTGGTGCTCTGTGGCACTGCGTGATTCCCTTGGTTACTTAGCAGCTGTTTGTCTGACCTAGAGAGGTTGGTAGCTGGGGCAGCTCCTGCAGAGCTGTGCTGAAATCCTCCTGGAAGGTGGGCTCTGGTTTATTTATCTCCAGCAGGTAGATAAGTCACTGTGATAACATTGCCCTCTTAGTGCCTGTAAATTTGAAGCTCTCTTTGCTGGAAGCACTGAGTTCCTTAGGCTGCCATAGCCTTAATCTGCAAAGAAGGTACCTTTCCATGCCACACTGTGGTGGTGCAGCTGATATTTGCGCCAGGTGAAAATGAAAAGAAGCAGTAATAAGGGGGTGAAAAACAACAGTCCTGCAGGTGTTTTTCATACGTTCCTATCCTATATCATTTGTTCTGGGTATTTTGCATTCATATGGCAGCACCGCATCTTGGATTGCATCCTTAACGGGGTTACAAATCCTTACCATAGTGCTCTTCAATCTGCTGTCACTCAGCCCTAATTGATGTCACATTATGATGTTTCTGTTTTTGTTTGCTTTGGGTTGTTTTTTTTTCCCTTGGTTGGTTGGTTTTCGGGTGGGAGGGTTGGAAGGGTGTTAAGAGAGAGCGGTGATGGGGAGGAACGGTGGTTCCTCTCCTGGGGAACTCTGCAGGGGCTGCCGTGGGCTGCAGAGAAACAGGAGTGTTCCTTGTGAAATGCTGAGCGTCCTCGACTCAAGTGGAGCTGTCGCTTCAGGAAAGAAGTGTGCCTGTAGAGCTGGACCCTGTATCAAGGGAGAATTCACTGCATCGAGACTCGCCCGTTGTCCTTTGAGTGCAGGACAAGTTAAGCCATGCAGATACGCAGCAGCCACATCAACTTTCTTCCCAAATCCTGAATCGCTTCTCTTTTCTGAATTAAATTGTTGTAAGCATTTCTTCATGCTTCTCAAAGCTGTGAGAATTTGTGCAGCACTTCTGTTTGGGATTTTTAAATCCAAGGTTGTATGCAGTATTCAGTATTAAAATACAAATATAATATCACAGTTGGTTTCAGCAGACTAAACCGATGATAAACCAACTGATGAGGATTTCTGTTCAGGATCTAAACTGAAACACAAGCTTGGCTGTCAAGGCTTGCTTTGCTTCTCCCTTTATAAATTGTGATTTACAATACTTTTAAATATAATAAATACAAGAGGAGCTCTGGCTGTACAGGTATATGGAGCCCTTGTCCCAAGCTGGGCAGTTGTTCCAGTAATTCTCTGGCTCCTCTGCTTTTCCTTCCTTCTTGGCCTCTGCACTTAGCCTGGTGTGAGTCTGGTTAAGCTAACCTGCCATCTGACCTTTTCCTTCAG
Seq C2 exon
GACTTCCTAACGGATCTGGTGATGTCTGAGGTGGATCGCTGCGGGGAACACGATGTCTTGATCTTCAGGGAGAACACACTTGCTACCAAAGCTATTGAGGAATACCTGAAGTTGGTAGGGCAGAAGTATCTCCATGATGCGCTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000004323:ENSGALT00000006891:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.043 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0016825=C2=WD(100=43.8)
A:
NA
C2:
PF0061614=RasGAP=PU(27.3=95.9)


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:
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]