Special

GgaINT0048004 @ galGal4

Intron Retention

Gene
Description
heterogeneous nuclear ribonucleoprotein A3 [Source:HGNC Symbol;Acc:HGNC:24941]
Coordinates
chr7:15330119-15331542:-
Coord C1 exon
chr7:15331390-15331542
Coord A exon
chr7:15330245-15331389
Coord C2 exon
chr7:15330119-15330244
Length
1145 bp
Sequences
Splice sites
5' ss Seq
GTGGTAAGA
5' ss Score
8.24
3' ss Seq
ACTTCGTGAATTTATTTCAGGTA
3' ss Score
8
Exon sequences
Seq C1 exon
TCAAAGGTGGCAACTATGGAGGTGGTCCTGGCTATGGCAGCAGAGGGGGTTATGGTGGTGGTGGAGGACCAGGATATGGAAACCCAGGTGGTGGATATGGAGGTGGAGGAGGAGGATATGATGGCTACAATGAAGGAGGCAATTTTGGAGGTG
Seq A exon
GTAAGATGCTAGCTCAAATTAGCTGACCCTTTTCTCATTCAGGTCTGAGTAGGATAGTGCAGAATGCTGTGTTACACAATTCTCCTCCCTCTGGATCAACTTTGATTAAATTATGCAACACTAATTTGCTTGGAACTTAATTTTCACAGAGTAGCTGCTGTAAACGTGTGGTGGTAGAGTAGGAGAACTTCAGTTTTTGTCCAATTGAAATATGCCGTTGGGTATCAGTTTGTACCACGTGGATGGTGTCCTCCTTTGTGAGGACTAAATGTCTTATGTTTATGGAAGCTTTATTGTCTGGTTGTGAAATGAGGTTCCTCAATAATTTTTATAAGAGCAGTCCTTTGGCCTATTTTGCCTTTTGAAATAACCAGGAACCACGTTATTACGTGGCTGTTTTACAGCACTAGCAAGTGTAAACCCTGGATGGCATGGAAGACATAAAACAGAAGTCTAGCTGTGTCCTGTAAAATCAGTTCGGCCATGTTCTTATTCTGTGTTGTCAGTGTTAATATCTTTGCAGGAGTTTCAAAATGATATGGTTAGTTTCTAAATCTGTGATTGCTTCTGGAGAGGCCTTCAATGACGTGTTTCTTGTCAGGGTATACCACAAACACTAAAACATGCGTGGTTCTTGACTAGAATTTTTTGGGGAAGAAGCAGTAGGAACATGCAAGGACTCAGTGCGAGTTGAGGGGGCTAAGCTGCAAAATCTACTGCACAGTTACGAATACCTTCTGGGGTATTTATGCGCTCATTACAGTTTTATCACTTTTTACAGCAAATAAAAATTGCTCTTGGCTTGTAGTTTATGGGATTGTCACGTACAGAGCACTGAACAGTGGAAGAATGATGGTGAAACCGGAGTGTTTATCTGAGTTGGGAGGCATTAACTTTGGCCTACCATGTTAATTTCAAATTGCTACTCAAACCTGTATGAACTTTCTAAGATAGCCTGCTATTTTTCTTCTTCAGTGATATACCGACTTCTCATCTTGGGAATGCTAAGGGTTTTGCTGTCATATGTGCATTGCAAGTAGAGGTAGCGTGCTCAGTGCTTGCAAGTCTATTATAAATTGTTTGAAATAGCTGTTGCAGTTTACACTGAATGTCAGAGTTTCATGAACTTCGTGAATTTATTTCAG
Seq C2 exon
GTAATTATGGAGGCAGTGGAAACTACAATGACTTTGGTAACTACAGTGGACAGCAGCAGTCCAATTACGGTCCCATGAAAGGTGGTGGCAGTTTTGGTGGTAGAAGTTCAGGCAGTCCCTATGGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000009250:ENSGALT00000038715:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.288 A=NA C2=0.767
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
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CAAAGGTGGCAACTATGGAGGT
R:
CACCATAGGGACTGCCTGAAC
Band lengths:
278-1423
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]