Special

BtaINT0063160 @ bosTau6

Intron Retention

Gene
Description
formin-like 1 [Source:HGNC Symbol;Acc:HGNC:1212]
Coordinates
chr19:45518056-45518573:+
Coord C1 exon
chr19:45518056-45518219
Coord A exon
chr19:45518220-45518471
Coord C2 exon
chr19:45518472-45518573
Length
252 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGC
5' ss Score
8.07
3' ss Seq
CTGACAGCCTGTGCCCACAGGAA
3' ss Score
7.43
Exon sequences
Seq C1 exon
TGTCCCTGGACAGCGTGCTGGGGGATGTCCGCTCCCTGCAGCGAGGCCTGGAGTTGACCCAGCGGGAGTTTGTGAGGCAGGATGACTGTGTGGTGCTCAAGGAGTTCCTGAGGGTCAACTCACCTGTCATGGATAAACTGCTGGCAGACAGCAAGACAGCTCAG
Seq A exon
GTGGGCTGGGGCTGGCCCCCGGCCAGGGAGGCGGGGAGGCTGTGGTGGGGGTGAAGGACCACCTAGGTAGGGTTGTGTAGCCAAGGCCTGGAGCCCTGTGACCCGGGAAGAACACCTTAGGGGATGGCACAGGAGGTGGCAGCCACCTGCCTGGAGGAGGAGAGATGAAGTGGCCAGTGTCCTAGCGGGTAGAGAGCAGTGGTCAGGGCCTTAGGGGTCTGGGCTGGTGAGGCTGACAGCCTGTGCCCACAG
Seq C2 exon
GAAGCCTACGAGTCTGTGGTGGAGTACTTCGGAGAGAACCCCAAGACCACATCCCCCTCCATGTTCTTTTCCCTCTTTAGTCGCTTCATCAAAGCCTATAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000004196:ENSBTAT00000034825:22
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=0.029
Domain overlap (PFAM):

C1:
PF0218118=FH2=FE(14.7=100)
A:
NA
C2:
PF0218118=FH2=FE(9.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTCCCTGGACAGCGTGCT
R:
TGATGAAGCGACTAAAGAGGGA
Band lengths:
254-506
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development