Special

HsaINT0186026 @ hg38

Intron Retention

Gene
Description
zinc finger MYM-type containing 4 [Source:HGNC Symbol;Acc:HGNC:13055]
Coordinates
chr1:35387454-35389082:+
Coord C1 exon
chr1:35387454-35387604
Coord A exon
chr1:35387605-35388909
Coord C2 exon
chr1:35388910-35389082
Length
1305 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAG
5' ss Score
9.06
3' ss Seq
TTATCTTTCCTGATTTTTAGGTT
3' ss Score
11.51
Exon sequences
Seq C1 exon
GGCAAAATGTTTCAGTTCTGTGGCAAGAATTGTTCTGATGAATATAAGAAAATAAATAATGTAATGGCAATGTGTGAATATTGTAAAATTGAGAAAATTGTAAAGGAGACTGTTCGGTTCTCAGGTGCTGACAAGTCATTCTGTAGTGAAG
Seq A exon
GTAAAGACAGAAGATTATCTTACCTACTGAGCATGTTGGTTGTTTTAAAGCAGTTGATGATGATTTAAGCTTTCACTGTCTAAGTTAATCTGTTTTATTGTTTATGTATAACGTAAATGCCTTTTCGATTCATTTACACTTAGTTCATTCTTTTTTGATCTAGTTTTCTTATATTATGTAGCTGTTAAAATGAAGTGAAAGATTTGCAAAGTATAATGCAGAAGAAGATGATGTGAAAAACATTTAACATCCTTAGGTTCCCCATTATTAGGTTGATCGGGACCTCAAAGAGCTTCTAGTTCGTGTACTTATTTCTAAATGGGATGCCTTAAATTATGGTAACATTCTAAGTTTATACTTTTATTGTCTTAAACAGCCATTATATTTCTGAATATAAATGGCTTGAATATGCAAATTAATATGTGGAAGATTGTTTTCCTTAGATAACTCTTCTATATGTTTATAATGTTTTATTTTACTCTAAAGCTGTATTAGCCTTCTAGAGCAAGGGCTTTCAAACCTTTTGATAACACCAAAGAAGAAATACATTTACACTGTGACCCAGTATATTTTCACATACCTAAATAAAAGTTTTTTTTGTTTTTGTTTTTGTTTTTTGAGACAGAGTCTTGCTTTGTCACCCAGGCTGGAATGCCATGGAGCGATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAACCTCCCGAGTAGCTGGGACTACAGGCACCCGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGCTTCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGACCTCAGGTGATCCACCCACTTTGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTACGCCCAGCCCCAAAAGTTTCATGAAATAAAATCGATGCAGTTTAATATTTTCTCTTCTGTGCTATCCTGTCTTATATCATTTAAAACAAAAACAAAAACAAAGCAAAACAAAAACTAGTATAGATACTCTAAAAAATCAAGATACTCTGTGAACTGGTCAGGACCCAAGTGTGAAAACTTTGTCCTAGACCACTTATTTTTCTTTTTTTTGTTTTTGTTTTTATTTGACATGGGGTCTTGCCATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGCACTCCTCCCGCCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACTGCACCGGGCCTGTCCTAGGCCATTTAAAGTTGCAGAAAACTAATACTTCTACCTAATGTTAATTTTATCTTTCCTGATTTTTAG
Seq C2 exon
GTTGCAAATTGCTTTATAAACATGACTTGGCAAAACGCTGGGGAAATCACTGTAAAATGTGCAGTTATTGTTTACAGACATCTCCCAAATTGGTACAGAATAATTTAGGAGGGAAAGTGGAAGAGTTCTGTTGTGAAGAATGCATGTCCAAATATACAGTTTTGTTCTATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000146463:ENST00000314607:13
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF064679=zf-FCS=PD(34.1=27.5),PF064679=zf-FCS=PU(85.0=66.7)
A:
NA
C2:
PF064679=zf-FCS=PD(15.0=10.2),PF064679=zf-FCS=WD(100=67.8),PF064679=zf-FCS=PU(2.7=1.7)


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:
GGCAAAATGTTTCAGTTCTGTGGC
R:
GAACAAAACTGTATATTTGGACATGC
Band lengths:
318-1623
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