Special

HsaINT0101779 @ hg38

Intron Retention

Gene
ENSG00000145794 | MEGF10
Description
multiple EGF like domains 10 [Source:HGNC Symbol;Acc:HGNC:29634]
Coordinates
chr5:127445457-127447684:+
Coord C1 exon
chr5:127445457-127445693
Coord A exon
chr5:127445694-127447556
Coord C2 exon
chr5:127447557-127447684
Length
1863 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
3' ss Seq
ATTTCCTTCCCTTCTTGCAGGAA
3' ss Score
12.77
Exon sequences
Seq C1 exon
CTGGTGTTATCATAGTTGGAAATCTGAACAGCTTAAGCCGAACCAGTACTGCTCTCCCTGCTGATTCCTACCAGATCGGGGCCATTGCAGGCATCATCATTCTTGTCCTAGTTGTTCTCTTCCTACTGGCATTGTTCATTATTTATAGACACAAGCAGAAGGGAAAGGAATCAAGCATGCCAGCAGTTACCTACACCCCTGCTATGAGGGTCGTCAATGCAGATTATACCATTTCAG
Seq A exon
GTAAGAGCAGAGGCAGGAGAGGCATTTTGCTTCTTGAAAAGTTAAATTTCATTCGGGTTCTTTAAAACTGGGTGTTTGGCTGTGCTGTCCATTGTTTCTGTCAATTCTCATTGAGAGAATTCTATGTTTGGAAAAGGTATACATTGCTAGAGATGAGTTTTTTATTTCAACAATAGTAAATTGTCATTCTGTGGTTTGCTATAAGGGTTTTAAAATTGAGCTCATTGTGTTTGTGGTTTAGATTTAGGGAATTTCAATCCATAAGGAGCTTTGTATCCAGCCTCAAGCTTTTGTCATATGTGAGGGGGGTGAGGAGGAAGAGAGGATGATAAGTTTACCAAGGTCATGGATCAGATTAGGGACCAGTTCTCCTGTCTCTGAATGAGGGTACTTTCTATGTGCTTCCCAGCCTCTCCCTAGGCCTACCCGAATCGTTAACTGAAGGGAACAAAGTTATATCAGAAACAGCTTTTTGGTATTAGCAAGAACCAAGGCAGCCCTTTAAGAAAACTCTTGATTTTTTCTGTTCTGTCACAATGCCTCATAAAAGGAAAAATAAAATTATAATCAATCATCAGTAGAAGCAACCATTTACATGGAGGAATTTAAAAGTTTAAAATCTTTATTACTTTTTGGGTGATTATTGAAGGCCTTCTGGTTGGTTACATGTTTAAAACTACAAAATTCCGTGGAAATATGAGAAGTAGCTGATTTACATAGTAGTGCATTTTCAGTGCAGAATTATTGTGTCAAGAACTCAAGTGTTTAAAAAAAGGAAAGTTGCAGAGTAGCTTCAAATGATACCTTCCCAGCTGTACCAGCCCCAAAGCAAAGAGCAGTTATCTGTGGATACTGTGAACAAAAGTTCTCTGAAAAGGAATTTGGGGGAAAGAGATTTTATTCCAGTGAACGGTTTGCAAACCCAGGAGTTGCAGCCAGTGTAAAATGAAAGTGCAGTTCAGAGAACAAAGGGAAGGCTTGGGTTTTATAGCAAAAGTCCCCACCCAGCTTCCAATCAGGCCCTTTTAGGAAAGTGAAGGATTGAAACTGGTTTAATTCTAATTGATCAGTGCAGCTGAGTTCTGGTTGGTTGACACAGCGGAACCCTGATCCTTTGATAAAGCTAAGCCCTGATTAGCTAAGGCAGGTAAGCTCTGATTGGTTGGTTCAGCTGAGCTCTGAAAGACCCAAAGATAAAAAGCTGGGTTTTCAGGGAACTCAGAGTACAGGTGTGATCCTTAGTCAGCAAAGGCCTGCTTGACTCGATTTTAAATTTAGGCCTAGGCAGCCACTCCTATGGATCTTAAATAATTGGTTCTTTCAGTTTCACATTTGTTCACAAGCTTTCATACTTTTCCAAGGAGGCAGTTAGGAAGGTAGAGGCCTGTTGCTTCTAGAAGCTTTGCTGAGTAGGCTGGGCAGGAGGAGATTCTGCCCAGCTTGTGATATGGAAGGAGTCCGGACATTTGTTCAGTTATTTATTTATTTGTTTTTTTATTTAGAGATGGAGTCTCGCTCTGTCACCAGACTGGAGTGCAGTGGTGCGATCTCGGCTCACTGTAACCTCTACCTCCGGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCATGCTACCGTGCCCGGCTAATTTTTTTTGTACTTTTAGTAGAGATGGGGTTTTACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTCATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCTCGCTGGGCCTGTTTTGTTATTTTGATTCCCTTTTTTCACACACATTTATGGGAGCCTGCTGCCTTAACCATTTCCTTCCCTTCTTGCAG
Seq C2 exon
GAACCCTTCCTCACAGCAATGGTGGAAACGCTAATAGCCACTACTTCACCAATCCCAGTTACCACACGCTCACCCAGTGTGCCACATCCCCTCACGTCAACAACAGGGACAGGATGACTGTCACGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000145794:ENST00000274473:21
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.013 A=NA C2=0.349
Domain overlap (PFAM):

C1:
PF0005319=Laminin_EGF=PD(18.9=8.8)
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:
GTTGGAAATCTGAACAGCTTAAGCC
R:
CAGTCATCCTGTCCCTGTTGT
Band lengths:
343-2206
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