Special

HsaINT0187453 @ hg19

Intron Retention

Gene
ENSG00000198546 | ZNF511
Description
zinc finger protein 511 [Source:HGNC Symbol;Acc:28445]
Coordinates
chr10:135123280-135123792:+
Coord C1 exon
chr10:135123280-135123481
Coord A exon
chr10:135123482-135123667
Coord C2 exon
chr10:135123668-135123792
Length
186 bp
Sequences
Splice sites
5' ss Seq
ATGGTGGGT
5' ss Score
6.18
3' ss Seq
TGACACGGTCTCCATTTCAGTAT
3' ss Score
8.01
Exon sequences
Seq C1 exon
GGTGCCCGCGTTTGCCTGCCAGGTGGCCGGCTGCTGCCAGGTGTTCGATGCCCTGGACGACTACGAGCACCACTACCACACGCTGCACGGAAATGTTTGCTCCTTTTGCAAGCGGGCCTTCCCTTCCGGACACCTGCTGGACGCCCACATCCTGGAGTGGCACGATTCGCTCTTCCAGATCCTGTCTGAGAGGCAGGACATG
Seq A exon
GTGGGTGACAACTGCACAGCCGCCGAGGCCACCCCCCATTGGTGATGGGCTCAGAGTGCTGCCCCCAGCTCTCGGGTGCTCGGGCAAGGCCGGGGACACCTTTCCGCCCTTGGCAGCTCTGCTACGGGGGCATGGCGGTGGGGGAGGGCCAGGGGTCAGAGGGAGGTGACACGGTCTCCATTTCAG
Seq C2 exon
TATCAGTGCTTGGTAGAAGGCTGCACAGAGAAGTTCAAGACCAGCAGAGACCGGAAGGATCACATGGTGAGGATGCACCTGTACCCCGCGGACTTCCGGTTTGATAAGCCAAAGAAAAGCAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198546-ZNF511:NM_145806:3
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.095
Domain overlap (PFAM):

C1:
PF0009621=zf-C2H2=WD(100=33.8)
A:
NA
C2:
NO


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:
ACTACGAGCACCACTACCACA
R:
TGGCTTATCAAACCGGAAGTCC
Band lengths:
254-440
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains