Special

HsaINT0186036 @ hg19

Intron Retention

Gene
Description
zinc finger, MYM-type 4 [Source:HGNC Symbol;Acc:13055]
Coordinates
chr1:35864465-35865177:+
Coord C1 exon
chr1:35864465-35864644
Coord A exon
chr1:35864645-35865082
Coord C2 exon
chr1:35865083-35865177
Length
438 bp
Sequences
Splice sites
5' ss Seq
CAGGTTTGT
5' ss Score
7.44
3' ss Seq
CTTTCTGCTGATTATTATAGACT
3' ss Score
6.35
Exon sequences
Seq C1 exon
ACCAAGGAAGTACATACAGTGGTGATCTTGAATCAGAGGCAGTATCTACTCCACATAGCTGGGAGGAAGAGCTGAATCACTATGCCTTAAAGTCAAATGCTGTGCAAGAGGCTGATTCAGAATTGAAGCAGTTCTCAAAAGGGGAAACTGAACAGGACCTGGAAGCAGATTTTCCATCAG
Seq A exon
GTTTGTGTACAGTAACCTGTCCACTGAAAGCTTTTTATTTTAAAAGATCGGTACAACTCTGAATTGACACTATTAAGCAGTGCCAATTGTTATTGATAATAACAGTGTAATGTGTTAGAGGTCATAATCTAGAGCACAAATAGACCCTGGCTTTGTAGGTGTTAATTCGTACCATATTGTTCTTATAAGTGGTTAATGTGGTTAAAATTTTTTTTAACCTTTCCCGTAGTAGCTATATAAGAGGTTTTCCTGATTGTTAATGAAGTTTTCATTTATGCACTATATCCTTGGTTTAAGTCTATAAGTGGAATCCTTATTTTATCACAAACAAACTAATGAATATAGTGATGATTACCTGATATTTCTTTACTAGTCTAAGTCTTTATTTAAATTTGTGAGTTATTTACCTCATGTTGTCCTTTCTGCTGATTATTATAG
Seq C2 exon
ACTCCTTTGACCCACTTAATAAAGGACAGGGAATCCAGGCACGTTCCCGAACAAGACGACGACACAGAGATGGCTTCCCCCAACCCAGACGAAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000146463-ZMYM4:NM_005095:22
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.880 A=NA C2=1.000
Domain overlap (PFAM):

C1:
NO
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:
ACCAAGGAAGTACATACAGTGGTG
R:
CTTCGTCTGGGTTGGGGGAAG
Band lengths:
274-712
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains