Special

HsaINT0101770 @ hg38

Intron Retention

Gene
ENSG00000145794 | MEGF10
Description
multiple EGF like domains 10 [Source:HGNC Symbol;Acc:HGNC:29634]
Coordinates
chr5:127420044-127422772:+
Coord C1 exon
chr5:127420044-127420207
Coord A exon
chr5:127420208-127422669
Coord C2 exon
chr5:127422670-127422772
Length
2462 bp
Sequences
Splice sites
5' ss Seq
CAGGTATGC
5' ss Score
9.37
3' ss Seq
TGATGCTGTTTTCCATGCAGGAT
3' ss Score
10.64
Exon sequences
Seq C1 exon
GCTGGCACGGGGTGGACTGCTCCATCAGATGTCCCAGTGGCACATGGGGCTTTGGCTGTAACTTAACATGCCAGTGCCTCAACGGGGGAGCCTGCAACACCCTGGACGGGACCTGCACGTGTGCACCTGGATGGCGCGGGGAGAAATGCGAACTTCCCTGCCAG
Seq A exon
GTATGCACAAATCAGCGCCCTGACGGAAAACGCCTATGAGGAACTGATGTTGTAAAGTTGGCTTCTTTTTGCATTTTTCCTGACTTCAAGTGGCTCACTGTGAACCCAACTTCGGTAACTACTGGAAGAATCCAGGTATTTGGATTCAAATTGGACGTAGGATTGGAAAAGAGATAGACATGGAAACTGGTTAGATAGGCTCTGCGAGAATTTCTTCCTTCTTTTCCTTCATCTTGTTCAGTTTCCTCAACCCCCACCCTTTACTTTCTGTTTCTTATTCACCCATCTCTTGGTGGCAGCCAGTGAACAGTACTGGTCTCCAAATATTTTGTTTCCACTATCATGGAAATCTCCCTGCCTTTATGGTAGAAAGTGGCAGGGAGTTGAAAGGAGGGTGGTGACTGATGTCATAGAAATGCTCATGGAAGTGTTGAAAGAAGGTTTGGAAACAATGTCTTTTAACATAAGTATCTCTGGAGCCACAAAAATTTCTTAAGATGTCCCTATAGCTCACTCTATTCCCTTGACCTACTTTGGAGATACAGGTCATTAGAAATCTCATACTGCATCTACCTCAAGCTGTCAGGGAGTGCAAACGGGAAGTGCATTCTGGAGTAAGCTGCTGATTTCTTTTCCATCACTCTTTCTTTCTATAGCAATTATTTTCTCCTGAGCCATTAGGCATTCTCTCTGTGGTGTGTGTTCTCTGCCTCCAGGACATCATCTGATGGCGAGTTAACAATGTGACCCCCTGAACTGGGCCCCTCGAGAAGGGCCTTCCACAATGCTCTTGTCTCTCTGGGCTTCCTCCTCATTAAGTACAACCCACTTCCCAAAATAGAAAGGATCCCACTCATGGATATCCCATGGACAGAGCTGTCAGCTTTGCTGCCTCTCATCACTCTAGTGAACAAATTATCAGTACTTGGAGATGAGCTTGAAGATCACTTTTTACTCCCTATCTGATTGTAGACAAAGCAAAGCCCCTGGCACAATCTCGTCCTTTTTCATACCTTAGAGGAGTTAGTAAATCAGTGAAGGCTGAGGGTTTAGTGGTTCATATCATGACAAAACTAAATCCTGTGTAGCTGTATCAAACATTGGTGGGGTCTACAAAATGATTGTTTTCTTTTTCTTATTTTAACAAGTTCTAGACAAATAATTATTCATCTAGCACCCACTACCTGTCTATGCTGGTTCCCATGTTCCTCCTCTGTGGTAATTCTGTACCCCTGTTTCTCTTAGTTCTTGGGTGGTGTTGGGAAGGCTTGTAGTGCCTCCCTCATTTCCCAGGATCTGTGGTGAAAGAGCTGAACTTTCCATTCTTTCTCCATAAACAAAACAATCATGTCTATGAGGAGTCTTGTCTCCATCAGACCATCCAAACTGACGTGCACATGAAAGTATAAAAGATCTGGAAGGGGAGGAGCAAGGAGGTGTGTCAACTCATACTTAGGACTGTGAGTCAGGATATTTTGTGTGGCTTAGACTTCTTCCTGAAAAGCAGGATAATAATCAGAGAAAAGTAACAAAATATCTTCATTTTTCTTTATAGTACCATGTATCTCGTTGGCAACTTATGGCAATGAACTTAATTCAATTAAAACTATAATTTTTAAGATTAGTTTATAATTTAAAATTTTTTTAAATTATAAATTTTTTTATATTTTATAAAATATAAATAGGCAGGAGAATGGTGTGAACCCGGGAGGCAGAGCTTGCAGTGAGCCGAGATAGCGCCACTGCCGTCCGGCCTGGGTGAAAGAGTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAATGACCCTGACCCACACAAAAAAGCTCTAAAATTATAGTTTTAAAACTATAATTTTATAATTTAAAAAATTTTTAAAGTGTGTTGGCATGATTGGCTTCACTATTTATATGTCCCAACCGTTGTGTCAGGCATAAACTAGGGTTTGAGTGACTTTAAAACACTGACTTCCTGGAGCCTATATTTTGGGGACTAAGAAGACATAGAAAGAGGTGATTAAGATGCATCCCTCTGGCTGGGTGCGGTGGCTCACGCCTGTAATCCAAACACTTTGGGAGGCTGAGGCGAGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACAAGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCTGGCAAGGTGGCAGGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGAATTCCTTCAACCCGGGAGGCCGAGGTTGCGCTGAGCTGAAATCACACCACTGCACTCCAGTCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAAAAGAAAAAAATAAATAAAGATACATCCCTGTAAGAAGCGTTTGGGACAGCAGGGTACTGTATGTGAAATGGCTGACAGTGGCCTTTTCCTCTTCTGTTGTGGGATTTCCCAGGCCCTCATTGCTGCCTTTGATGCTGTTTTCCATGCAG
Seq C2 exon
GATGGCACGTACGGGCTGAACTGTGCTGAGCGCTGCGACTGCAGCCACGCAGATGGCTGCCACCCTACCACGGGCCATTGCCGCTGCCTCCCCGGATGGTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000145794:ENST00000274473:13
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:
NO
A:
NA
C2:
PF126612=hEGF=PU(69.2=25.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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
  • Pre-implantation embryo development