Special

HsaINT1022053 @ hg38

Intron Retention

Gene
ENSG00000254402 | LRRC24
Description
leucine rich repeat containing 24 [Source:HGNC Symbol;Acc:HGNC:28947]
Coordinates
chr8:144524110-144524719:-
Coord C1 exon
chr8:144524441-144524719
Coord A exon
chr8:144524279-144524440
Coord C2 exon
chr8:144524110-144524278
Length
162 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGC
5' ss Score
8.69
3' ss Seq
ATCTGCTGTCCTTACTTCAGCGA
3' ss Score
7.57
Exon sequences
Seq C1 exon
ACACTGTTCCTGCAGGACAACAACATCGCCCGCCTAGAGCCGGGAGCCCTGGCGCCACTCGCCGCTCTGCGCCGGCTCTACCTGCACAACAACAGCCTGCGCGCCCTGGAGGCCGGCGCCTTCCGCGCGCAGCCGCGCCTGCTGGAGCTGGCGCTCACTAGCAACCGGCTGCGCGGCTTGCGCAGCGGCGCCTTCGTAGGCCTGGCCCAGCTGCGCGTGCTCTACCTGGCGGGCAACCAGCTGGCGCGGCTGCTGGATTTCACCTTCTTGCACCTGCCG
Seq A exon
GTGAGCGCCTGGGGTCTAAAGGGGCGGGATACTCCATTATGGCCCCTCGCCCTGTAGGGCTGGAATAGTTAGAAAAGGCAACCCAGTCTAGCTTGGTAAGAAGAGAGACATGCCCCCAACCTCGGCGCCCTTTTTCCTCACGATCTGCTGTCCTTACTTCAG
Seq C2 exon
CGACTGCAGGAGCTTCACCTGCAAGAAAACAGCATTGAGCTGCTGGAGGACCAGGCTCTAGCGGGGCTGTCCTCCCTAGCACTGCTGGACCTCAGCAGGAACCAGCTGGGCACCATCAGCCGAGAGGCCCTGCAGCCCCTGGCCAGTCTGCAAGTCCTGCGCCTCACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000254402:ENST00000529415:3
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=0.000
Domain overlap (PFAM):

C1:
PF138551=LRR_8=WD(100=65.6),PF138551=LRR_8=PU(0.1=0.0)
A:
NA
C2:
PF138551=LRR_8=FE(93.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Chicken
(galGal4)
Chicken
(galGal3)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TACCTGCACAACAACAGCCTG
R:
TGGTCCTCCAGCAGCTCAAT
Band lengths:
254-416
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains