HsaINT0108983 @ hg19
Intron Retention
Gene
ENSG00000169994 | MYO7B
Description
myosin VIIB [Source:HGNC Symbol;Acc:7607]
Coordinates
chr2:128391751-128392258:+
Coord C1 exon
chr2:128391751-128391864
Coord A exon
chr2:128391865-128392170
Coord C2 exon
chr2:128392171-128392258
Length
306 bp
Sequences
Splice sites
5' ss Seq
AAGGTGGGC
5' ss Score
7.93
3' ss Seq
TGTACCTTCCCCTTCCCCAGGTC
3' ss Score
11.49
Exon sequences
Seq C1 exon
ATGCTGGAGGTGGTTGCCAACACACGGGTGCGGGATGTGTGTGACAGCATTGCCACCAGGCTGCAGCTGGCCTCCTGGGAGGGCTGCAGCCTCTTCATCAAGATTTCAGACAAG
Seq A exon
GTGGGCCGGGCTGGGGCTGGGCAGACGGTGGGCGGACGGGCAGTGAGCGAGGCCCTAGGTGCTGCCTGTGGGGGCCTCAGCCTACCAGGGGCACCCATGCTGGACCAGGCTGCACGGCCAGGGCTGCTGGGACAGAGGTAGGTGGGGTCCTGGAGCAGAGCCAGCTCCACACGCCAATAGCCCACGCACAGCCGACTCCAGCGCAGCACCCAGGCCGTAGGCGGCCACTGGACCAGAACCCAGCAGGTTCTCAGGAGGACAGTCCCCGGAAGCCACCCAACTTCCCTGTACCTTCCCCTTCCCCAG
Seq C2 exon
GTCATCAGCCAGAAGGAGGGAGACTTCTTCTTTGATTCCTTGAGGGAGGTGTCTGACTGGGTGAAGAAGAACAAGCCCCAGAAAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000169994-MYO7B:NM_001080527:40
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=NA C2=0.033
Domain overlap (PFAM):
C1:
PF093795=FERM_N=FE(39.4=100)
A:
NA
C2:
PF093795=FERM_N=FE(30.9=100)
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:
CTGGAGGTGGTTGCCAACAC
R:
CTTCTTTCTGGGGCTTGTTCT
Band lengths:
199-505
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Genotype-Tissue Expression Project (GTEx)
- 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)