Special

HsaINT0187573 @ hg38

Intron Retention

Gene
ENSG00000118156 | ZNF541
Description
zinc finger protein 541 [Source:HGNC Symbol;Acc:HGNC:25294]
Coordinates
chr19:47528950-47529652:-
Coord C1 exon
chr19:47529577-47529652
Coord A exon
chr19:47529039-47529576
Coord C2 exon
chr19:47528950-47529038
Length
538 bp
Sequences
Splice sites
5' ss Seq
CAGGTGACG
5' ss Score
7.66
3' ss Seq
TTGGCTGTGTTCTTTGATAGGTT
3' ss Score
8.76
Exon sequences
Seq C1 exon
GTCGCCCTGGAGACTCTTCTGCTCCGAGGGCCCCACAAGCCACGGACACACCTGCTCGCTGACTATCGCTACACAG
Seq A exon
GTGACGGGGAAAGGCTGCTGAGCTGGTTTGGCCCAGCTGAGACCCCTATGAATCGGCCAGCTCTGTTGCAAGCTCTGCCCCTGCCTCCTGGAGTTCTCCTCGGGACCTTTGCCTGCCTTTCAGGAGGGCCTGTCCTTGTCGGGATGACTCAGTGGGCGCCACATTCTGCTAGTGGGATCCTGCTTCGCCCTTTCCCAGTGGTTTCCTTACGGACTCTGCCCAGCTGGAAGGGGAATGATCATGGCCAGGGGGAGGGAAGATGGGCTTAGGTTCAGTGGTTGAACCCATCAGCTCTGGAAACAGGATGCCAGGGCCCCCACCTGCCTTTAGCAAGCGACTGAAGCCTCAGTTGCCACATCTGTTAAGTGGGGCTAGTAGTGGTCCCTCCCTTCTGGAGACTTTTTGAGTTTTTTATGAGATTGGCACATAATTGGTACTCAGTAATGGCAGCTATAAATGGGAAGGTGGTCTGCATTTCAGCCATGGCTGTGGTCCCAGGACAAATGGCCTTCCCCCTGTTGGCTGTGTTCTTTGATAG
Seq C2 exon
GTTCAGACGTCTGGACCCCTATAGAGAAGAGGCTTTTTAAGAAGGCGTTCTATGCCCACAAGAAGGACTTCTACTTGATACACAAGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000118156:ENST00000391901:11
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.029 A=NA C2=0.010
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0024926=Myb_DNA-binding=PU(60.9=93.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains