HsaINT0065171 @ hg19
Intron Retention
Gene
ENSG00000161791 | FMNL3
Description
formin-like 3 [Source:HGNC Symbol;Acc:23698]
Coordinates
chr12:50048693-50050280:-
Coord C1 exon
chr12:50050187-50050280
Coord A exon
chr12:50048768-50050186
Coord C2 exon
chr12:50048693-50048767
Length
1419 bp
Sequences
Splice sites
5' ss Seq
GAGGTCAGT
5' ss Score
7.7
3' ss Seq
GAGAAAGTTTGCTCATTCAGGTA
3' ss Score
4.27
Exon sequences
Seq C1 exon
GACCAAAGCCCTTGTCTTAGAGCTTCTGGCAGCTGTGTGTTTGGTGCGAGGAGGTCACGAAATCATCCTTGCTGCCTTTGACAATTTCAAAGAG
Seq A exon
GTCAGTCTTTTCGCTTCGCGTGTGTGTGTGTGTGTTTGCGGGGGAGAAGGCAGGGAGCTAGGTTGGTAAGCACCATTTCCTGTGATCTGCAATGATTTTTAACATCCCAATGCTTGGCCAAGCAGCCTCTCTCCTGAACTCCCAGTATTTTTAAAACCAGAACTTTAGTCTTACTAGATCTTCAGGCCAGGAAACCTCCTGATTGGCCAGCTAAAGATACCCTCAGCTAGCTGAGGGCTATAGTCCAATGGTCCTAGTTGGGCCCTGCATCCAAATCACCTAAGGAGCTTGTTAAAAGTACAGATCCCTGTGCTCTAGTTCAGACCCACTGGAGGCCTGAGTATATGTACTTAAGTGACTCCCCAGATGGGAGTCTGATGCGGTGAACCCATTGGTAGAACCCAAAGCACATGTGTTTTGAAATGGGAGGAGAAGGTAAGCAAGGATGTCTCCTGATTTGTTGGCTGTTATTGGTGAGGGGAGAAGGAACTCCTGTGTGGAATTTCCCCCAGCCCCTGGGCCTGCCTCTGAAACCCCTATCTACTTGAACATAGGATTCTTCGACATCCAGCCACAGCTGGTGGTCCCACCCCTTCCTCTTCTTTGGACCTCTTCCCTAGCATCCATTGTTCAAGCCAGGAAATGGCTCTTCCTCCTTGAAGCCCAGAGGCTCAGAGGAGCCTCTAGACCCCTCTCAGAGAGGGCTTTCCTGTACACTGGCCCTTCCCCTGCATCCCCACTAGGACTGCAGCCTCCTGTCTCAGGCATGGCCTTCCTCCCTTCCTCCTTCTTTCCCTCCTTCCTTTAGTAACTTGGCAGCATCAGACCCCTATGTTTCTTCTTGGCCTATCCCCAGAGGCACCTAAAGCCCAGCTTAAGGGCACAGGCTTTACTGAATTCCCTCAGCAATTTGGTGGGGGACCACAGACCCAGAGCCAGATTGCAGGTCCCAGTTTTCTTTATTTTCTTTTTTGAGATGGAGTCTCACTCTGTGGCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACTTCCACCTCCCAGGTTCAAGCGATTCTTCTGCCTCTGCCTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCATGCCCGGCTAATTTTTGTATTTTGAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGTTCTTGAACTCCTAACCTCAGGTGATGTGCCCATCTCGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACCGCGCCTGGCCCCAGGTTTTCTTTTATAGTGTCCAGAATGGCCTATTTCATATATAGAGCTGTGGTTAAGCTTGGTCTGAACCAGTCCTTTGCCATGATGTTCCTAGGAGCCAGAGCGCAGGGGCTTGGGTTCTGCATGGAGCAGATCCTTTCACTGAGAAAGTTTGCTCATTCAG
Seq C2 exon
GTATGCAAGGAGCTGCACCGCTTTGAGAAGCTGATGGAGTATTTCCGGAATGAGGACAGCAATATTGACTTCATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000161791-FMNL3:NM_175736:9
Average complexity
IR-S
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:
PF063718=Drf_GBD=PD(19.7=43.8),PF0636711=Drf_FH3=PU(6.9=43.8)
A:
NA
C2:
PF0636711=Drf_FH3=FE(11.9=100),PF061486=COG2=PU(1.2=8.0)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
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]
SPECIAL DATASETS
- Autistic and control brains
- Pre-implantation embryo development
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)