Special

GgaINT0098648 @ galGal4

Intron Retention

Gene
Description
laminin, alpha 3 [Source:HGNC Symbol;Acc:HGNC:6483]
Coordinates
chr2:102843043-102843675:+
Coord C1 exon
chr2:102843043-102843182
Coord A exon
chr2:102843183-102843559
Coord C2 exon
chr2:102843560-102843675
Length
377 bp
Sequences
Splice sites
5' ss Seq
TTGGTGAGT
5' ss Score
9.27
3' ss Seq
TTAGCTTTTTCTGTTTTAAGGAA
3' ss Score
8.4
Exon sequences
Seq C1 exon
GTTCCTTCAGTGCTTCATTCTGCCCTCATTCTTCTGGCTGTCGGGATCAGGTGATTGCAGAAAACCAAATTGAGCTTGACATTTCTGAACCTGAAGTCTCTGTTACAGTAATGATACCTGACAGAAGAATGCTGGTTTTG
Seq A exon
GTGAGTTTATTACGTAAGTGTACTTGAAAATACTCTTCCAACTTTACCAGCCATTTAGAGATAGGTACAAAGGTGAAAGCTAAGAAGAAAGGATGTGATTTTTAATGTAGTGTTTCAAATTGTTAGAATCTTGTACACTGCTTTTGTTTTTAAGATATCATACACTGCTTTTATTGTATGCTGCTTTTAGAGTAAATTAGAGGAGGAGGGAGGTAACATATCTTCCAAGTATGTTTTCCTACCTTTTTGTTAAAATGTTATATTTTGGGGGGAAAATTCAGTACTCAGAAAGAAGTGACATTAAAAGATAGAAATGCCTCAGCTTGTTTGTTTTGTTTCTTTCCTGAAATGTACAATTTAGCTTTTTCTGTTTTAAG
Seq C2 exon
GAAAGTGTCTTAGTTGTTCCAGCAGACAGCTACAGTTACAAAATTCTTGACAAAAAGACTGTGGACAAGTCATTTGATTTTATCACCCAATGTGGAGGGAACAGTTTTCACATTGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000015056:ENSGALT00000024287:29
Average complexity
IR
Mappability confidence:
NA
Protein Impact

5' UTR

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

C1:
NA
A:
NA
C2:
NA


Main Inclusion Isoform:
NA


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TCCTTCAGTGCTTCATTCTGCC
R:
TCAATGTGAAAACTGTTCCCTCCA
Band lengths:
254-631
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]