Special

HsaINT0095575 @ hg38

Intron Retention

Gene
Description
lysyl oxidase like 2 [Source:HGNC Symbol;Acc:HGNC:6666]
Coordinates
chr8:23319885-23322281:-
Coord C1 exon
chr8:23322130-23322281
Coord A exon
chr8:23320053-23322129
Coord C2 exon
chr8:23319885-23320052
Length
2077 bp
Sequences
Splice sites
5' ss Seq
AAGGTGATG
5' ss Score
5.22
3' ss Seq
GCCTGCCTTTGTGTCTGCAGCTG
3' ss Score
10.53
Exon sequences
Seq C1 exon
GGATCGGACCCATCCACCTCAACGAGATCCAGTGCACAGGCAATGAGAAGTCCATTATAGACTGCAAGTTCAATGCCGAGTCTCAGGGCTGCAACCACGAGGAGGATGCTGGTGTGAGATGCAACACCCCTGCCATGGGCTTGCAGAAGAAG
Seq A exon
GTGATGGGACTGGACACCTAGAGGGGACTGTAACTGAGGCTGCAGAAAGTATAGCCACAGAGCTCTGGGGTGAACCCTGGAAGTGACCAGGTGCTGCTGCTAGTACTGCTGCAGACATTGCCACTTGGCATTTGCAATGTTTAGTTCCCCCTCGAACCTCGGGCCTGGCCCTGGCCCGGCAGCAGGCCCAAGCCCCTGTGTGCAGTGTGAGCTGGAAAGGCCCTGCCTCCTTGCATGTTAACATCTGAGGTGAGTTACCTCACCTCTGCCCCACCACCTCCAAAGACAGGCGTGGGACCGGCTAGCCACAACCTTATCAAAACACGGTGCAGCCTGGCTGTGCTCTGCTGGCTGGAGGCGTTCTCTTTCCTCTATTCATGTTCAGAAAAAAACTGGGCTGCCACACACTTCGCTCCCTTCTTTAAAACCCTGTGCTGCTGCCACTGAGAACCAAAGGAACAGGAAAAGGGAAATGCCTGGGCTGTTTTAAGAGACTTGGAAAGGGCTTGACCTTCCCTGGCATCCTCCTTGGGTGAGGAGGTGGAGAGGGTGAGGACAGAGGCTCCTGGCTGACCATGAGGTCCCATACGCTCCATTGTCACTGGTGAGGTCAGACCCCGCTCACCAGAAAGCCACACGGTTACCAGGATGCTGACGCTCTACGTGGGGCTCTGGGAATGGCAAGCTGTGTCCTTTGCTGAGTTAGAACTGCATGCCAGCTACACTGTGCGCTCCAGTCTTCTCTAGAAAATGAGAAAAGCCCCCCAGTGCATGAAGTGTCCAGATTCCTTCCAGAACAGTCAAACCCTTCTCTCTGTCCTAGAGGCCATCCCGGGCCTGGTAAGCCTTAACGCCTTGGAGCCTTGGCAGGTGCCCTTGGTGACCATGTGTTTTCCTGGCCCCAGAGGCAACGAGGCAGCCACATTCCGCAGCCAGAGCCTCTGAGACTTGCCTTGGCTTTAGGACCTAGAGCAGGAACACTGCTCTGGCTCAGGCAAGAGATGAGGGAGGGTAGGGAAGGACTGGAGGGAAGTGGATGCATTGGAGAGAGACGAGAGATAAAACCCACAGGTGAAGACCGACAGGATGTGAGATAAGAGAGTGGGAGATGTCAAGAATTGCTCCTCTGTTTCTGGCTTGAATAACAGCAGATTCAGGAGCCAAGAAACTATGATATGTGGCCAAGCCCACCCTTCCTCCTGGTTTTTTATTCGTTTGTTTTTTGAGACGGTCTTGCTCTGTTGCCCAAGCTGGAGTGCAGTGGTATGATCATAGCCCACTGCAACCTGAAACTTCTGGGCTCAAGGGATCCTCCCACCTCCCGAGTAGCGGGGACTACAGGTATGCACCACCATACCTGGCTCATTTTTTAAACTTATTTTTTTGTAGAGATGGGGTCTCACTATGTTGCGCAGGCTGGTCTCAAAACCCTGGGCTTAAGTGATCCTCCCACCTTGGCCCCGCAAAGTGCTGGGATTACAGGCATGAGCTACCATACCCAGCCTCTTTTTTAAGATAAAGTTGTATCGGAACATGGCCACACCCGGTCATTTAGGGTAAAGAGAAAAGACAGCAAGTTCAGATTTGTGATCTCTGAGATACCAAGTGGGGTTGTCAAACAGGCAGCTGGTTAGGTGGGCCTCAGACCAGCAGGAGAGCCATGGGACAAGATGCCAGTGGCTCTGGAACCCGCCAGGTAGGGGATGTGGCAAAGAGAAAAGTGCCCAGGCAGGAGTCTTGTGGGATTCCAACATGTCAAGGTCCCGAGGGCACCATCCTCCCAAAGAGCAGCCCCCCACTGATAGGCTCATGGGGAGCAGGGTCAGCTTCTGCTGTGGGGCTCAGTGGAGTCACAGGGCCTCCCCAGCTGCTTAGGGTGCCTGGGGTGGGGACCTCACTATAAGACCATGCTAGGCACAGCGCTGCCACCGGGGGCTCCCAAGGGTGCTGCTGAATCTGAGTGTGTCCCGGGCAGCACCACCTGGCTTAGGACTCCAGGACACTGGGGCTGATGGCAGCGTAGGGGGGAAGCTCCCTTGTCCCTCTTGGTGACCGTGGCCTGCCTTTGTGTCTGCAG
Seq C2 exon
CTGCGCCTGAACGGCGGCCGCAATCCCTACGAGGGCCGAGTGGAGGTGCTGGTGGAGAGAAACGGGTCCCTTGTGTGGGGGATGGTGTGTGGCCAAAACTGGGGCATCGTGGAGGCCATGGTGGTCTGCCGCCAGCTGGGCCTGGGATTCGCCAGCAACGCCTTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000134013:ENST00000389131:7
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:
PF0053013=SRCR=PD(42.3=80.4)
A:
NA
C2:
PF0053013=SRCR=PU(48.6=92.9)


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:
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]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development