Special

HsaINT0061443 @ hg38

Intron Retention

Gene
Description
mitoguardin 2 [Source:HGNC Symbol;Acc:HGNC:23621]
Coordinates
chr9:129059154-129060650:+
Coord C1 exon
chr9:129059154-129059271
Coord A exon
chr9:129059272-129060549
Coord C2 exon
chr9:129060550-129060650
Length
1278 bp
Sequences
Splice sites
5' ss Seq
TCGGTGAGC
5' ss Score
9.1
3' ss Seq
TCTCTCACTGCTCTTCCCAGAGA
3' ss Score
6.98
Exon sequences
Seq C1 exon
CCAGAGTCACAGCGGAAGGAGTTTGCAGAGAAGCTGGAGTCCCTGCTGCACCGTGCCTACCACCTGCAGGAGGAGTTCGGCTCCACCTTCCCCGCAGACAGCATGCTGCTAGACCTCG
Seq A exon
GTGAGCTGGGCCCAGTGCAGGTGGGGTGGGCGTGGAGGGTGGCAGGGATGGAGGTGAGGAGAAGTTGCGAGAACCGGGTCGTGGTTCTCTCAGTGCGTCCAATGAATCAGAATCCCCAGGGCTCTCCGACCTCGCGTGATCCAGCACCTTATGGCACAGATGGGGAAACTGAGGTGTTCCCTTCTCCATGGCAGGCTGGAGCAGAGCTGAGGTGAGGCCCAGAATCCCCAGCAAGTGCACCTGGCTCCATCCTCTTGGGTGCAGCCTTGGGGTTCGTGTGGCAGCATCTCCCTGATGGCTCTCCCAGGCCTTCGCTTCGAGTCCTTTCCTGTGGCTCAAACTGGGTGGGTGGATGGAGTGACTCACGGGAGGTTCACTCAGAGCAGGCCAAAGGCCAAGAACAGAAGTTCCTGTTGTTGGGTGCGCTGAGGTGAAATGATGTGACATACTGAGGGGGAACCAAGTTATTCTGCCAAACAGCCACTGTCCTCTTCGGACCCCTGCAGTGAATGACACCCTGGCCCCTCCCTGTGCACTCAACCCTGTGGGACCCTCAGACTCCTGAGGGTCCAGCTGCCTGGCTCTGCCAGTGGAGACACAGAACCGGAGTGGGTCGGCCGAGCCACGCACCCTGCCCTGGCTTCTCCCCACGTGCTCTGGGTGTGGTTTCTCTGTTGGAGGAATCTGCCTCCTCTGGCCTCCCTACATGGCAGAAAGGGCTGGGGGACCTTTAGGGTGGCCCGCCGCAGGTCTGTGGCCTTTGCTTATTTGCTCGACAATCCTTTCCTGAGCACCCTTGGAGGTCCACACCCCTCAGCCCTTGGGCGAGCACGGAGGGGAACTCCAGGTTAGTGGCTGTGGACTCTTTCGAGCCCTTGGTATCAATGGCTGAGTTTCAGCTTGTCAGAGGAGAGAGGCGATTTCCCCGGGGCCACACAGTTCAAGGTCCTCCCCCTGCAGAGCTTGGGCCTTCAGGCCTCAGGTCCAGCGGTGCAACCTGTGAGCCTGGCAGAGCCGCTCACCAGCCGAGGGCTCACACCTGAGGCTGACGACCTCCGAGGATGTCGTGGGTGTTGAAGGAGGTCACTCACTGAGGCGAGGAGTCCAGCGTCCTCACACAGAAGCGCTTGGCACGTCAGAGCTTTGCCATTGAGTGTGGGAATCACAGGCTCGGGATGAAGCCTCCCCTGGGCCTGATGGGGGACTTCGTGTACCGGGATTCCAGCTGAGCACTGTGTGGGGAGTCTCAGCCCCGCTTTCTCTCACTGCTCTTCCCAG
Seq C2 exon
AGAGGACCCTCATGCTGCCCCTGACCGAGGGCTCGCTGCGGCTGCGGGCGGACGATGAGGACAGCCTGACTTCAGAGGATTCCTTCTTCTCCGCCACCGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000148343:ENST00000358369:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.344 A=NA C2=0.306
Domain overlap (PFAM):

C1:
PF102654=DUF2217=FE(12.5=100)
A:
NA
C2:
PF102654=DUF2217=FE(10.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGAGTCACAGCGGAAGGAGTT
R:
GGTGGCGGAGAAGAAGGAATC
Band lengths:
214-1492
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development