Special

HsaINT0101788 @ hg19

Intron Retention

Gene
ENSG00000145794 | MEGF10
Description
multiple EGF-like-domains 10 [Source:HGNC Symbol;Acc:29634]
Coordinates
chr5:126732224-126734488:+
Coord C1 exon
chr5:126732224-126732470
Coord A exon
chr5:126732471-126734367
Coord C2 exon
chr5:126734368-126734488
Length
1897 bp
Sequences
Splice sites
5' ss Seq
CTTGTAAGT
5' ss Score
8
3' ss Seq
GTCACATGTTAATCCCTCAGCTG
3' ss Score
5.38
Exon sequences
Seq C1 exon
CCTGCGATGGTGATCACTGGGGTCCCCACTGCACCAGCCGGTGCCAGTGCAAAAATGGGGCTCTGTGCAACCCCATCACCGGGGCTTGCCACTGTGCTGCGGGCTTCCGGGGCTGGCGCTGCGAGGACCGCTGTGAGCAGGGCACCTATGGTAACGACTGTCATCAGAGATGCCAGTGCCAGAATGGAGCCACCTGCGACCACGTCACGGGGGAATGCCGCTGCCCACCAGGATACACCGGAGCCTT
Seq A exon
GTAAGTCACATGCTGCCCAGCAGCAGAGCAGAGCCCACCCACCCTCTCCATTCATGCTGCTGCTGCCATCATATTTCTTGTGCCTCAGTTTGCATTGCTGCCTGAAGAGTTACTGATGGGTCTAGGCTGCAGGCACAGTTATAGAGGTCAGCAGTGATGGCCACTAGGTGCTGCTGCTGTTTGGCCCTTGCACATCAGATCCCAGCCTGAATCTAAGGGTCAGCTTCCATGCTTTCCTTCTAGCAGGCAAAGAGAGAGAGGGTCAGTCAGGATGTTGTGTTGAATGGCACTATTTGGGGGTTGTTGGGGCATATTTGGGATTCTGTTTGGATCTCCCGAGAATATGTTCATTTATACTGCTGGTTGTTAATGGTCCATGTCTTTTTGCTCTTTGTGGCAATTAATTAGCTGGGGAAAGCTGGGTGGGTTCAGTGCATTAGAAGAGAAAAGGAGGAAGGTGTTAAAAATAATCCATAATAAAAGATTAACTCTTAGGGATACATACATTATTTAATGCTCATGGATACATATTGCTTTGTGAATGTGAAGATATATGTATTACATCTATGTAGATTTTGTGCACACACATAGTTTAATTCTTTCTGAGGAACATTCAAGCAACTACTTAACCTCCACTGTCTTTATTTTGTTGGAAGGGCATTCTTCAGTTCACTTCTATTCACCAACAGAATTAAGAGGCAGAAGTTGCTAAAAAAAAGTAAGAGATAGAAAAATCCTCTTCCCTTACTGAGAAAATTACATTTATAAATCAAAGAACTAAAACTTGAAAAAACAAAATGTGGCTGATTAGGTAAACACTTCCTGCCAACAGTGTTAAACGCCTGTAGAGTGGAGCTAAAGAAAAAAATTGCATTAGCCTAGAAAGCCCTGATTTTCAGAATTGATGATTATCTCAAACTGTTTAATTGTTAATATTGCTTTTATGGGTTTTCATCAAGACCACAATTGAACTGGGCTGTGGGAAACTTGGAGCAATTTCCCAGGAGAGCAGGAAAGACAAAGGCTTAAAGAAGAAGGGCCATGCGACACGTGGGTGGGTGAGGGAAGGGAAACTTGTCAGTCAGTAGGAGAGAACACCAAAAATGGATGATGAGAAGGAGTTCATGTCCTTTGCAGGGACATGGATGAAACTGGAAGCCATCATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACCGCATGTTCTCACTCATAAGTGGGAGTTGAACAATGAGAACACATGGACACAGGGAGGGGAGCATCACACACTGGGGTCTGTCTGGGGGTGGGGGGAAAGGGGAGGGAGAGCATTAGGACAAATACCTAATGCATGCGGGGCTTAAAACCTAGATGACAGGTTGATAGGTGCAGCAAACCGCCATGGCACATGTACACCTATGTAACAAACCTGCATATTCTGCACATGTATCCTGGAACTTAAAGTAAAATTTTAAAAATTAAAAAAAAAAGGATGATGAATATGTGCACAAAGGGTGTGATGTGCAACATCTCAATTTTCTTTGGGAACAGAACAAACATATAAACAAAAGTAGACTTAAACTGGAGCACAAGCGCTTTATAAGTGTTACATGAGAAGTTCCTGTCATCAATGAGTGTTTGGCCAGTTTTCTTCCTCAGTGTTCTCAGATAGGATAGCTTCTCTTCAAACCGAAATGGCTTTATTAGAAAGTACCCCAAAACAAAGGGAAGGACTGGGTGACTCCTCAAAGACACTTCCAGGCAATATGATTAATGTTCTTGATGTTAATTAATTAAATGAACAATTATTGAACACAGAAAGCTTGTCTATTTTGGGGACCCTGGGTACAGTGAACCCGAGGGTCATGTGTCTGGGAAATAACAGTGTCCTTTGTCACATGTTAATCCCTCAG
Seq C2 exon
CTGTGAGGATCTTTGTCCTCCTGGTAAACATGGTCCACAGTGTGAGCAGAGATGCCCTTGTCAAAATGGAGGAGTGTGTCATCACGTCACTGGAGAATGCTCTTGCCCTTCTGGCTGGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000145794-MEGF10:NM_032446:7
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:
PF0005319=Laminin_EGF=WD(100=55.4),PF126612=hEGF=PU(84.6=13.3)
A:
NA
C2:
PF126612=hEGF=PD(7.7=2.4),PF079748=EGF_2=PU(83.9=63.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTGCGATGGTGATCACTGGG
R:
GGGCAAGAGCATTCTCCAGTG
Band lengths:
354-2251
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