Special

HsaINT0186035 @ hg38

Intron Retention

Gene
Description
zinc finger MYM-type containing 4 [Source:HGNC Symbol;Acc:HGNC:13055]
Coordinates
chr1:35398413-35399043:+
Coord C1 exon
chr1:35398413-35398466
Coord A exon
chr1:35398467-35398863
Coord C2 exon
chr1:35398864-35399043
Length
397 bp
Sequences
Splice sites
5' ss Seq
AAGGTTTGT
5' ss Score
7.81
3' ss Seq
TTGTTATCTATATATTTCAGACC
3' ss Score
8.61
Exon sequences
Seq C1 exon
AGTCCCAAACTTCTGAACACGAACTCTTTCTAGACACCAAGATATTTGAAAAAG
Seq A exon
GTTTGTAGTTGAAAATATGTTTTGATTTTTAGAAATACTACCCTCTGTTAGAAACCTATAAAATATTAGTACCCTTGGATTTCATATTTGTAATTTTAACTATTTGTAAGGGGTATCAGATGTATATGAAGTGTACTAATTTGTAGTGAGAATAATAAAAGCCACTCAAATGTTTGTTTTAAAAATTAATTGAGATAATGCTTTCAATTGCCTACCAAAAATATGAATCCAGTTCTTTGAGACTGATGAACAAGTTACCTCATTCTTGAGTGTACCTAGGTAATTGTCCATCAACCGTATCTCATTTTTTGGTATTTAGGGGTTCAGGAAGTTTTCCGAGCATGTCAAGATGAGGCTATTTTATTTTGAGGGCTTAATTGTTATCTATATATTTCAG
Seq C2 exon
ACCAAGGAAGTACATACAGTGGTGATCTTGAATCAGAGGCAGTATCTACTCCACATAGCTGGGAGGAAGAGCTGAATCACTATGCCTTAAAGTCAAATGCTGTGCAAGAGGCTGATTCAGAATTGAAGCAGTTCTCAAAAGGGGAAACTGAACAGGACCTGGAAGCAGATTTTCCATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000146463:ENST00000314607:21
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.596 A=NA C2=0.880
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:
AGTCCCAAACTTCTGAACACGA
R:
TGGAAAATCTGCTTCCAGGTCC
Band lengths:
230-627
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains