Special

GgaINT0042860 @ galGal4

Intron Retention

Gene
Description
ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) [Source:HGNC Symbol;Acc:HGNC:74]
Coordinates
chr6:17104171-17105576:+
Coord C1 exon
chr6:17104171-17104230
Coord A exon
chr6:17104231-17105461
Coord C2 exon
chr6:17105462-17105576
Length
1231 bp
Sequences
Splice sites
5' ss Seq
TTCGTGAGT
5' ss Score
7.9
3' ss Seq
TGCCTGGTGTTTGTCTGAAGTCT
3' ss Score
4.21
Exon sequences
Seq C1 exon
TGGCATTATGAAGCCAGGCTTGAATGCTATCCTGGGGCCAACAGGGAGCGGCAAATCTTC
Seq A exon
GTGAGTACTTCTTTTTGCTCTTCAAATGGCCAGTCACCTGTTCAAAGGGGATGTGGGACAGTTAAGGTTGGGAGAGGATATGAGGGACCCTCAGGCTCAGACTTTGGTGTGCCTGTGAGAAATCTGGTGATGCAGTTTGACCTCACATCCTGCCCCTCTGATGTCAGCTTTGCTGGCGTTCTTGTCCTGCATTTGTGCCACACCCTTCCTATCTGTGGTCTGTGTTACTGTCATCAGCTTTGATGGTGGCCTGAGTTGAGATACCAGGGGAACAGGAGCGACTTAAGCTCAGGTGTGGGCTCTGCTCCAGACCTGTCACGGTGTGGAGGCGGGGGCAAACTCTGTCAGGGGTGGGAGGGAGGTTGTCACCTGTGAAGCTGCTGCAGCAAGACCTCCTCAGAGATGCAGACCGCTCTGATGGCTGCCAGAAGTAGGGTATGATGTCATTCTGTAGGATACCTGCTGTAGATCATCCATCACCCAGTCTGGATGTGGCTCGGTGGTAGGAGTGCATGTGCTTGGAATCTCTGGATGAAAGCACAGAGAATACTTTGCAGGCTATTTCCAGCCAGTACTGATGCTGTTTTCTCTCTTGTGTAACCATAGTAAAAGAGTGCTGCGTCACTCTTCCTTTGAGAAGGTCAGGGACAGGTGAGTATGGCCAGGGTTCACACAGGTGTGTCTTTGTTGTGATCCTTGATCTTCCCCTCTAGGAGACTGTCAGGATGTTTCCAAGAACTAAGCTCCAACAGGGCAGTGTTCACTGAGCTAGCAGACAGTCTGGCCTCTAATTTGCAGTAAGGAGAATCCAGGCATATGTTAAAACAAAACGACTTTATGAAATTAATATTTAATCCAGTCTTGTTTATGCCCATTTGGATTAATTTCCTTGAGATCAAAGTAGTTTCTTCTGTGCTCCATTGGCTGGAGAGCAGACTGCAGCTGCTTGGCAGGGTGCTTTTGTGTGTGTGTCTGAGGTTAGCTGTTAATATGGAGCCCGAGCTAATGTCTGCAGGGGGTTGGCAGCCGTGAGGGTCTGAGTACTTCGGAATTGCTGTGGCATACCTGGCACATGAGAATCCTGCAGAAGGCCCCAGAGTAGAGGATGCCCCTTTGAGTGCCCTGTGTTTGGACTGCAGCAGCTGTAACTGCAGTGCTGACTTGTAGTACTTGCTCAGTTGAGATAGAGCAGTTGTCATGGCAAAGCCTAATGCCTGGTGTTTGTCTGAAG
Seq C2 exon
TCTGCTAGATGTGCTGGCTGCCAGAAAGGACCCAGCAGGCCTGTCTGGAGAAGTGCTCATAGATGGCATCCCACAACCTCCAAACTTCAAGTGCATCTCAGGATATGTTGTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005792:ENSGALT00000009304:2
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.048 A=NA C2=0.026
Domain overlap (PFAM):

C1:
PF0000522=ABC_tran=FE(13.2=100)
A:
NA
C2:
PF0000522=ABC_tran=FE(25.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
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]