Special

GgaINT1001670 @ galGal4

Intron Retention

Description
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:F1NWS8]
Coordinates
chr2:42173441-42174877:+
Coord C1 exon
chr2:42173441-42173531
Coord A exon
chr2:42173532-42174205
Coord C2 exon
chr2:42174206-42174877
Length
674 bp
Sequences
Splice sites
5' ss Seq
TTGGTGAGA
5' ss Score
6.29
3' ss Seq
TATTGGTTCTTCCTCTCTAGATA
3' ss Score
9.41
Exon sequences
Seq C1 exon
ATTGATGATACTGGAAGATTTCAATTATTTGTTTGGGAAAGACAACAGGATGAAAATTTGGAGAACATCACAAATTGTACACTTTGCTTTG
Seq A exon
GTGAGACATTTTACTTATTTCAGCTGTTGTATTGCTCTTTTTACACTTTCAGCAACGTTCTTATGTTTTTCAATAAAATAATTATTCTGGGCAATATGGATAGTAAGAATTAGAGTTTTAAAAACACAAAAAGCTATTTAATTTCTGTCTCAGCTGTGTGCAACCAATTTTTCTATTTGGCATTTATTTTGTAACAGAAACACACTCTAATATCACGTTTCTGAGATACCATGCTCATTTATTATAAATTTTGTATTTTGAGGTAGAGAAAAGCTGCTAAATAATAACAGTGTTTCAGAATGCTTATCAGTGGTCTGAGATAAAAATATATATATATATAGAGAGAGAGAGAGAGAGAGAGCTTGCTGCAGTGTCCTCTGCCATGTTTAGATTTTGATAGAAGAAAAATTCTCAGGGAAATTCTGTTCATAAGGTAAAACTTAACACACGAGTTTTTGATCTCATACCTGACTAATTTCCCATAGAATCTCAAAACCTGGTTCAGCAGGATTCATCCCTTGTTGCTTGTAAGAAAAAATAAGATTTCTGGTCTGTAAATTGATTGTTTTAAATCAAATTTAAGGGAAAAAATATGAACAGGACTCACATTTTTTTCAAACCATTGTTTTTGTTGTTCTGCTAAATAGTTTTGTTTATTGGTTCTTCCTCTCTAG
Seq C2 exon
ATAAATGCAAGCCCAGTACCAACTGCAAAGTGCCCATTTCTCCACCTCTTCTGATGGATATGGATATTACTTACATCATGGACAGCTCTCGCAGCATCAGCAGTGAAGATTTTCAGAGAGCCAAGGACTTTGTGAGCAACATGATAGATCAGTTTGTCATTGCTGAACAGCCAAGTGAATCTTTAGGAGGCACCAGAGTGGCATTGGTACAGCAGGCTCCCAGAGGCTTCCTACCTGACAGAAACAAAATCCCTGTGGCCTTGGAATTTGATCTAGAAACATATAACAATAAAGATTTGATGAAGAAACATATCCAGGAGTCTGTTCACCAACTAGAAGGGCCATCAGCCATTGCTTCTGCATTACAGTGGACAGTTGAAAATGTATTTTTTAAAGCTCCCAGACAAAGAAAACACAGGGTCGTATTTGCAATAGTTGGAAGCAAAACAAGCACACAAGACAGAGAGAAGCTAAGAGAGATTTCACTTGGAGTCAAGTGCCAAGGATTTACCATGTTCACTCTTGCGCTTGGCAATGATCTGAGCGACAGTGAGCTGATGGAACTATCAAGCTCTCCCACAGATCAGCACTTATTGATATTGGGTAGGACTTCAAAGTCTGAGATGATATATGCTCAGAGATTTGCCCGGGCGTTTCTAAATCTGCTACAAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000011567:ENSGALT00000018866:46
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=0.018
Domain overlap (PFAM):

C1:
PF0009223=VWA=PD(12.8=74.2)
A:
NA
C2:
PF0009223=VWA=WD(100=86.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TCACAAATTGTACACTTTGCTTTG
R:
AGTTGGTGAACAGACTCCTGGA
Band lengths:
358-1032
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]