Special

GgaINT1005013 @ galGal4

Intron Retention

Gene
Description
alpha-2-macroglobulin-like 1 [Source:HGNC Symbol;Acc:HGNC:23336]
Coordinates
chr1:75541400-75542025:+
Coord C1 exon
chr1:75541400-75541511
Coord A exon
chr1:75541512-75541915
Coord C2 exon
chr1:75541916-75542025
Length
404 bp
Sequences
Splice sites
5' ss Seq
CAGGTAATT
5' ss Score
8.55
3' ss Seq
GTCTTACTGCTTTCATTCAGAGA
3' ss Score
7.62
Exon sequences
Seq C1 exon
ACAGACAATATGGGTTGCTTCTTCACAAATGTGACACTATCCTTCAGCCAAGACTTGAGGTACTATCGGGACAGCATAGTTGCAGAGGCCTCACTGTTGGAGGATGGCACAG
Seq A exon
GTAATTCTGGAAATATCTCTGGGAAGAGGCATGTGAAGATACAATAATCATAGTAAGAATGCCACAGACTTTCAGACTCGCAAGAGCTTTGAGGTTTTTCAGCCCATTGAGGCCTGCCATCTAACCTCATGGATATTGGCAGAGCCACAGATTCCTGAAGGCATGACACTCAGAGTGTCTGTGGTCTAATCTCACATGGTAAAGCTTAGGGACCTTTCTAAGGGATAGAAGATAATGTGAAGGAAACCAGATACCCAGAGCCTTGGATAAGTCATCTTGGTATGAAATATATATGCACAAGTACATCAGTATTACCAGTGGGTTATTCTACAGGCAAATTGCTGACAGGTGCTTGGTTTCCCTGTTTTCCTCCCTTATGTTTCTGTCTTACTGCTTTCATTCAG
Seq C2 exon
AGATACAGGTCAATGCTTCCCATAAATTACTCATCTCCAAGATTGGCGGAATGGCCTTGTTTGATGATGTGAATTCTTACTATCACGCTGGAGAGATGTACAGAGGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000019254:ENSGALT00000037222:10
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=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Human
(hg38)
No conservation detected
Human
(hg19)
No conservation detected
Mouse
(mm10)
No conservation detected
Mouse
(mm9)
No conservation detected
Rat
(rn6)
No conservation detected
Cow
(bosTau6)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
ACAGACAATATGGGTTGCTTCTTCA
R:
CTTCCCTCTGTACATCTCTCCAG
Band lengths:
222-626
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]