Special

HsaINT0101769 @ hg19

Intron Retention

Gene
ENSG00000145794 | MEGF10
Description
multiple EGF-like-domains 10 [Source:HGNC Symbol;Acc:29634]
Coordinates
chr5:126754812-126755899:+
Coord C1 exon
chr5:126754812-126754932
Coord A exon
chr5:126754933-126755735
Coord C2 exon
chr5:126755736-126755899
Length
803 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
3' ss Seq
CTGGCGTTCTTGTCGCACAGGCT
3' ss Score
6.92
Exon sequences
Seq C1 exon
GGAATTGACTGCTCTACCCCATGCCCTCTGGGAACCTATGGGATAAACTGTTCCTCTCGCTGTGGCTGTAAAAATGATGCAGTCTGCTCTCCTGTGGACGGGTCTTGTACTTGCAAGGCAG
Seq A exon
GTAAGAATGGGTAAATAAGTCTTTAATTTGATCCTGGTCACGTTATCTCCTAAAGACACAAAAAAGAAAAACCTTAACCAGGGTTCTAGCTCCAGTTGCACCAAAATTCAGTGTCTGACCTCCGCAAGCCCCTCATCCAGTATGGGCTGGAACGCTTTCCTGAGTGAAGGGAAGAGGCTCACATTAGATGATCTCTGAAGTCACTGCCAGCTCCAAAAGTCTCTGTGTCTGTGCACTTTTGGGAAGAGTAAACAAGCAGACATGTGTTCATGCCCCTAAATTGACTGGCTTGGAATCATGACAAGAAACGCAGCCAAGCACCAATTTTATATGAGCACTAGAACGTGTCCATCCATAGGTGCAGCCAGGATCCTGGATATACACAGTTGCTGGTTAATGGGGTCCTGCTTTAAAGATGGTGTTGTGTTTTCAAGCAGAATCCTTTGTCTCCCTTCCATATAAATATTTCACTTTCCTGATCTGAACAAAACTCAGCATTCCACAGTGTGCATCACTGCCCATTAAAGGTGCTTTGACTCTATATCTCTTTTTCAGTAGCCCACTAGTATGCAGTGCTGGCATCCTCGACAGATCACACAACACACATGGCTGTTTGGGTCGTCAGGGGTGCCTTCTGTTCATTTCTGATGGAGGCCTAACTTGGCAGAACCAGTGTTCTCTGCTGCTGTGGCTGGGGCTTGCATCTCCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACAAGGCTCTCTGCTGCCTTTGTTCGCTCACGTGCTCTGGCGTTCTTGTCGCACAG
Seq C2 exon
GCTGGCACGGGGTGGACTGCTCCATCAGATGTCCCAGTGGCACATGGGGCTTTGGCTGTAACTTAACATGCCAGTGCCTCAACGGGGGAGCCTGCAACACCCTGGACGGGACCTGCACGTGTGCACCTGGATGGCGCGGGGAGAAATGCGAACTTCCCTGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000145794-MEGF10:NM_032446:12
Average complexity
IR-S
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:
PF126612=hEGF=PD(23.1=7.3),PF126612=hEGF=PU(46.2=14.6)
A:
NA
C2:
PF126612=hEGF=PD(46.2=10.9),PF0005319=Laminin_EGF=PU(67.4=56.4)


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:
ATTGACTGCTCTACCCCATGC
R:
GGCAGGGAAGTTCGCATTTCT
Band lengths:
280-1083
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