Special

GgaINT0047749 @ galGal4

Intron Retention

Gene
Description
formin-like 2 [Source:HGNC Symbol;Acc:HGNC:18267]
Coordinates
chr7:35012377-35014482:+
Coord C1 exon
chr7:35012377-35012453
Coord A exon
chr7:35012454-35014388
Coord C2 exon
chr7:35014389-35014482
Length
1935 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGGC
5' ss Score
9.88
3' ss Seq
GCGGCTTGCTTTCTTTGCAGGAC
3' ss Score
9.84
Exon sequences
Seq C1 exon
TATGGATTCAATATGGTCATGTCGCACCCGCATGCCGTTAACGAAATTGCACTAAGTCTGAACAACAAGAATCCCAG
Seq A exon
GTAGGCTGTGCTTGCTGTTAGAGAGTTTAAGAAGTAGTTAAGTGAAGAGTAGAGGGATTTTCATGGATTTATGTACAAACCTGTAGCGAAAATCAGCCTTTGCTCTGACTCAGATTCAGTTTGTGTTACAGTGCAGTTAGATGGGCGATTGCCGTTTGGTTCCATTGGTCTCAGAAGCTGCTGAGTCTGCAGCTCTGCCTTTGCTGCTCAACTGCTGCTGCAGTGCAGACTCTGCTGATCAGGAGCAGCTTTGCATGGGATTTTCCTGAAGAAACTAAATTTTCTGCAGTAAATTTTGTTCTAGCCATCTTCAAGTTTGAGTTTCTGTAAGAGCACATTTTATACTTGTTCTGCCTCTGTACAGTGCCTGACGAAATGTCGGGTGTTTCTTCAACCACAGCAGCAGTCCTCTAATGACACTGTGGAGCTGATTGCTGCAAGGTTATGTCCCCTTTCCCCCCTGCACGCATTTGGGAGCTGGCGCCTACATCCAGCCAGACTGGAGCTGCAGGCATCCCACATACCTGGTGATGCCAGAGCTGAGTACTGGTGTTTTCCAGGGAAGGGAAAAGCAGGAATGAGACAAAACTAAAGTGCACCATATAGAGAGAGCTCCCTTGCCTAGACTGCCTGCTTGCCATGCAGTGTTCTGCTTGAAACCTTGGCCTGATGGAAGTGGGTCCTTCCTTCCTCTCTTCTATTTAGGCTTAAGTCAGCAAGCATGAAGGGGAAGGATACAGGAAGTTTGTTGTGATCATTTGTGTCCTGTCCCTGGAAATCAGGTGATGAAGAGACAGCTTAGCGATGAGTGATGCCAGCACAGCAGGTCCTGTCCCATCCCTGCCCCATCGCAGATGCAGCAGGGGAGTGGGTGCCGTACCTGACGCTGAGACCTGGGCATCCTCCTGGCATCTCCATAGCTCACAGCCCTTCAGAGGATGTTGCCAGTGGGCCATAGGGAGAGCTCCTCGAGCCTGTCTGAAAGAGCTTGGGTTTTCTTCTTGTGGCAGGACAAAAAAATGGATGAGTAAGAATTGAAAGTGATCCGTGTAAAATTTCCTGGGGAAGTGAACATTTTATCTGGTTTCCAAAGATAACCTTGACACTTTGAAAGCCAAAAGGTATTTCTTTTTCTGCAACATCTGGTTTAATGCTCAAGCATGAGACTAATTTCATGTGTGTTTGCATGGTTTCGGTATCTGCTCCCAGCTCATCTGGCTTTAAGATCCCATTGGTGCTTTTGCCTCATGTGAACTGTGTAAGAGAGAACTGGGGATTATTTATGTCAGAGCTATACCGAGTGTTGCATGCTTTTCTTTCAGCAATCAGTTGTATCCTCCCCTCCCTGATATGCTGTGTTAGCTGTCAGTCAGCGCCCAGATTTCAGGTACTGGAGGGGGAGGTGTGCTAAGGCACCTTGTGTTCACTTCAGCAAACCACATCTTGCATTTTTTGTGGCTGTGAATAACACAACTTGTCACAGAGGATAACTCAGATGTGCATCAGGGCAGTGCAGATAGAACTAAAAGCTCTGGCCACAGAGGGGCTGAGACATGGGCTGCTCCTAGCAGCGATGCGTTGCCCCGTGTGCCTCCCCCTGTGGGTTTGTGCAGGAGAGCTCCCACAGTGCCAGCTGCCAGGCTGATGCAGACACCATTGGTTTGCTTGGATTTCCTCAAGTACAATTTGTGATGTAAATTTGTGCATCTTTTGGGAAATATTAAAATGGGGGAGAGTTGCACGATCCTGGGAGGCTCAAACTACCCTGGATCAGACGCTGCTCAGCATTCTGTGTCCTGCAGGTTTGCTTGTCTCAAGAGGCTGAACCACTGGATGCAAAGTACTTCTCCCGGTGGCTGCACGGCACTTTGCAAACAGGTAGAAGGTATTCCTCACCCGCTTGTCACTGACTGCTGCGGCTTGCTTTCTTTGCAG
Seq C2 exon
GACAAAGGCCCTTGTCCTAGAGCTCCTGGCTGCTGTTTGTCTCGTCAGAGGAGGGCATGAAATCATTTTGTCTGCGTTTGATAACTTTAAGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000012525:ENSGALT00000037752:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.179 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF063718=Drf_GBD=FE(33.3=100)
A:
NA
C2:
PF063718=Drf_GBD=PD(18.7=43.8),PF0636711=Drf_FH3=PU(6.8=43.8)


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:
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]