Special

HsaINT0020750 @ hg38

Intron Retention

Gene
ENSG00000156030 | ELMSAN1
Description
ELM2 and Myb/SANT domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19853]
Coordinates
chr14:73726604-73726972:-
Coord C1 exon
chr14:73726830-73726972
Coord A exon
chr14:73726708-73726829
Coord C2 exon
chr14:73726604-73726707
Length
122 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
TCATGCTCCTGTGGATCCAGTGG
3' ss Score
3.73
Exon sequences
Seq C1 exon
ACGGATCAACGTGGGCTCCCGGTTCCAGGCAGAAATCCCCTTGATGAGGGACCGTGCCCTGGCAGCTGCAGATCCCCACAAGGCTGACTTGGTGTGGCAGCCATGGGAGGACCTAGAGAGCAGCCGGGAGAAGCAGAGGCAAG
Seq A exon
GTGAGGAGGGGCCTGGGGGCAGCAAGTGAGGGCAGGCACATGGGTGGGCCAGGCCTCACCCTGCCCAGCCCCGCCCTGAACGTGGTTTCCTCCCCTCCCTCCTCATGCTCCTGTGGATCCAG
Seq C2 exon
TGGAAGACCTGCTGACAGCCGCCTGCTCCAGCATTTTCCCTGGTGCTGGCACCAACCAGGAGCTGGCCCTGCACTGTCTGCACGAATCCAGAGGAGACATCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000156030:ENST00000394071:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.064 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0144819=ELM2=PU(79.3=93.9)
A:
NA
C2:
PF0144819=ELM2=PD(19.0=31.4)


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:
ACGGATCAACGTGGGCTCC
R:
TGTCTCCTCTGGATTCGTGCA
Band lengths:
242-364
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development