Special

HsaINT0186045 @ hg19

Intron Retention

Gene
Description
zinc finger, MYM-type 4 [Source:HGNC Symbol;Acc:13055]
Coordinates
chr1:35826795-35827390:+
Coord C1 exon
chr1:35826795-35826856
Coord A exon
chr1:35826857-35827219
Coord C2 exon
chr1:35827220-35827390
Length
363 bp
Sequences
Splice sites
5' ss Seq
AGGGTAAGT
5' ss Score
10.45
3' ss Seq
TCCTTTATATTGTGTTTTAGGAT
3' ss Score
12.81
Exon sequences
Seq C1 exon
CTAATCAAGTTGAAGAAACATTACATACCCATTTACCACAAACCCCAGAAACAAACTTTAGG
Seq A exon
GTAAGTTTTCAGTGTGTATGTAGATTGCTGTAACTGTGACAAGTGTCAAAGTTTTCTTTATGTCAGTTTCTAAATTCTAACAATGTATTAGGTAGAGCACTGATTTTTTTTTTTTAATTTGCTTAATATTTGTTTAAGGTCATCATCGGAGACATTCTAAAAAGCCTCAAATCTTAGGGTCTTTATTTGTATTTGGTATTTGGACATATAACACAATTACTTTTAGGCGTAGGCATAAGATCCAAAAGCTAATGAATGTCCATAGAGTTCTTCATTTCCAATGAGCTTTTCTTTGGGTGTTAAACCTGAAGAGGAATCATTTTAAAATCTGAATATTTATTAATCCTTTATATTGTGTTTTAG
Seq C2 exon
GATTCCAGCTACCCATTTGCCAATAAAGAATCCATTGGTTCGGAACTGGGGAATTCCTTTGCATCAAATATTAGAATTAAAGAAGAACCTTTGGATGATGAGTATGACAAAGCAATGGCACCACAGCAGGGACTACTAGACAAAATAAAAGATGAACCTGACAATGCTCAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000146463-ZMYM4:NM_005095:4
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.905 A=NA C2=0.691
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAAGTTGAAGAAACATTACATACCCA
R:
TGAGCATTGTCAGGTTCATCT
Band lengths:
227-590
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains