Special

RnoINT0094022 @ rn6

Intron Retention

Description
major histocompatibility complex, class I-related [Source:RGD Symbol;Acc:1593291]
Coordinates
chr13:72779706-72781058:-
Coord C1 exon
chr13:72780798-72781058
Coord A exon
chr13:72779982-72780797
Coord C2 exon
chr13:72779706-72779981
Length
816 bp
Sequences
Splice sites
5' ss Seq
CAGGTGTGA
5' ss Score
5.29
3' ss Seq
ATAGCCTGTGTATGTTTCAGGGC
3' ss Score
8.79
Exon sequences
Seq C1 exon
GGACCCACTCTCTGAGATACTTTCGTCTGGCTATTTCGGATCCTGGCCCTGGAGTCCCTGAATTTATCTCAGTTGGGTATGTGGACTCACACCCTATCACTACATACGACAGCGTCACCCGACAGAAGGAGCCAAGAGCCCCATGGATGGCGGAGAACCTGGCGCCTGACCACTGGGAGAGGTACACTCAGCTGCTAAGAGGCTGGCAGCGGACCTTCCAGACAGAGCTGAGGCACCTGCAGAGGCACTACAACCACTCAG
Seq A exon
GTGTGACTGCAGCAGCGGGGGATGAGCACACCCCCTCACTGGCTACTCCCCAGAAGAGCGCCCCTGGGCTGTGTATGGCAATGCCACTGGTTGCTTATATCCTCTCTAGCCTTTGGCAAAACTTTGAAAACGAGGTTGTTCGTTGTGTATTCTCTGTTCACCATCTCCCCTGTGGCTCGTTCACACTGACCTTCTGTGGAAACCCCTTATCCCTTGCCCCCATATTCCTATCCCATTGGTCCCTTTATCCCTTGTCCTATATTCCTATCACATTGGTATTCAACAATCTTTTCTTTTCTCATTCTAAATTTGCTTACCTTGGGACTCAACTTCTGATGGCTTCATGATTTGTTTATTTCTTTTTTTTTTTCCGGAGCTGGGGACAGAACCCAGGGCCTTGAGAAACGACNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCCGATTTGTTTATTTCTACATGGAAACTTACGGTATTAATTGTCCCAGATACATTTCTAGCCCCTGCATATCTCTTGCTCCTATACCGCACTCAGAATAGCTATGAAATTTATCAATGAATCATCCCAAAGATAGGATAATTCCTCAAGGCAGGCATCACTGTGATCCTTTGGCATGCCGTAGGTGCCTCACCAATGTCTGTGAGTAGGTGGCTCTGCAAAACAGGAACCTTCGGGAACCCAAATATGCAGGCCTGTGTGGTGGTGTCTTCTGAGGCAAAGAGTTCTTCCAATCATGCTCCAGTCGTGCCACTTGAGAAGCCTCTCTCTGTCTCTGTTTAAAGCCATCTGTCCATAGCCTGTGTATGTTTCAG
Seq C2 exon
GGCTTCACACCTACCAGAGAATGATCGGTTGTGAGTTGCTGGAAGACGGCAGCACCACAGGGTTTCTCCAGTATGCATATGATGGACAAGATTTCATTGTCTTCGATAAAGACACCCTCTCCTGGCTGGCTATGGATAATGTGGCTCACATCACCAAGCGAGCATGGGAGGCCAACCTGCATGAGTTGCAATACCAAAAGAACTGGCTAGAAGAAGAGTGCATTGCCTGGCTAAAGAGGTTCTTGGAGTATGGAAGTGATGCCCTAGAAAGAACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000003522:ENSRNOT00000004694:2
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.034 A=NA C2=0.007
Domain overlap (PFAM):

C1:
PF0012913=MHC_I=PU(49.4=98.9)
A:
NA
C2:
PF0012913=MHC_I=PD(50.0=94.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGCCCTGGAGTCCCTGAATTT
R:
ATCCATAGCCAGCCAGGAGAG
Band lengths:
354-1170
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]