Special

HsaINT0101775 @ hg19

Intron Retention

Gene
ENSG00000145794 | MEGF10
Description
multiple EGF-like-domains 10 [Source:HGNC Symbol;Acc:29634]
Coordinates
chr5:126774131-126776559:+
Coord C1 exon
chr5:126774131-126774259
Coord A exon
chr5:126774260-126776430
Coord C2 exon
chr5:126776431-126776559
Length
2171 bp
Sequences
Splice sites
5' ss Seq
AGAGTAAGT
5' ss Score
9.35
3' ss Seq
TGTCCTCCCTCCTCCCACAGGAT
3' ss Score
14.05
Exon sequences
Seq C1 exon
CATGTCCACCTGCCCACTGGGGCCCAAACTGCATCCACACGTGCAACTGCCATAATGGAGCTTTCTGCAGCGCCTACGATGGGGAATGTAAATGCACTCCTGGCTGGACAGGGCTCTACTGCACTCAGA
Seq A exon
GTAAGTGACAAGCCTTCTGAGGCTCACCAAGGGGAGCCTTGTCCAAGGAGGAAACAGCCTTACCCTCCGCATGCGTGACTGGAGCTCAACAAAGGTCCCTGAGGTTGGAGTACTTCCCTCTCCTAATGACCTGTAGACATATAAATTTCTCTAAGTGATTAAGAGCTACTTCATTCCAAGTATTCTGTCTCTAGGTTCTATCTCCACTGAGGTAGAGCAATGCTGTGTGATGGTATGCAGTTTATTTCTCTTCTCTCCTTTAACCAAATCATATTTATATGGATCAAATTCTCAATCCTTTAACAGCACAAAAGTTAGGATAAGTATAGAGATTAGAAAGGTAGAGAAGACAACAAGCCTCACTGCCTGATTTAATGTGCGCTCTTGGAAAAGGTGGAGTTCCGTGTTTTTCGAATGGTAGCAAGCTTCAGAATCACCTGGAGGACACAACAAACACAGAAGCTAGTTCCATCCCCAGAAAGCCGGAAGCAGCGAGTCTGGGCTGGCACCTGAGAATTGCCATTTTTATCAACTGGTAGTAATGCCAGGCTGGGACCATGCTTTGAGAGCCACTGCCCTAGTTCTTTTCCCCATTTTGTAATTCATAGCATCCTAACCATTTTTTCTTCCATTAGGCTTTTAGCATGATAGGATATAGTGTGCAAAGTACTTACTCCAAAGCTGAGCATCATTGGGGAAGGAAGATCATTCTCTGACCTCTTACCTTCGGTTGAATAAAGGAGACAAGAAAGGAAGGCATGTGTTATGGTTAAGTACTAATAATAGCGTATATTTTAAAATAATAGCAAGAAGCTGAGGAGGACAGATGGGTCTGAAATTGAGCAATTCTTATTTAATACTAATTAGAGTACATAATTAAAGAATAGGCTGAAAAAGTCTTAGAAACTTTCTAGAAGATAATGTAGACCTTGAACCAAGAGTTGAAAAGGATAATTGGCAAGGAAGGTAGCTGGCCCAAGCATATTCTTCAGAGTTCGTATATCTATAAATATTGTTTAACTTCTTAGAGAAAGGTACTTGTAAGATATTATTTATAATTCTAAAATTAGAACGTGCTTCAAAGAGAGAACCCTTTTTCAAGTGCAAGTAACATGATATAGTGGGAACAACATGGGGTCCAGAGCCAGACCTCCCTGTGTTTGAATCATGGCCCTGCCGTCCTGCCAGTTGCCAGCTGTGTGACTTAGGGTACTTGGGGCTTAGTTCCTGTCTACAAGACGGGAATATCCATCCCTGCATTTCTGGCCTGCTGTAAAGATTAAACAAGAGAACGCATGAAAAGAATCTGGCACAGAGTAGGTGCTAAATAAATGCATGACAGCAGGGAGTCATCGGTGCATACTGGCATCTGGGCACTGCCTCTGCTTCTTGAAAGTTCCATAAGAAAATGAGAAAATGAAAAGCATATGTAATATTTGGAAACAATCATTGAATCAGCCTGCATTGAATCTTTCATCACGCCAGAGATCCCCAAGACACTCTTGCAGGGCAGCTGCCAGCCCATGTAAGCCAACAGAATTTGTGGGTGTCTTTAGCTCAAGAGACTCGCCGGTCTAAGCATTGAAAATCATGCAGCAGTGTGAAGGGTTATTGCTTTTTACAAAGCACCTGTGAAGTACAATTGTTTTTTAAGGTAAGCATTCTAGTACACCTCTTCAGGGAAGTTGATATTATCTAAGATAATAACAGATACAGTGGACAAGGCTAGTAGCAACAATAGAGATGTTCTGTACTACAAGTAAAAGCATACAGGTAATTTTAATATAAAGTACCCGTCTCAGTCCATTGGAATTTGAGTCCAGGATTCTAGTAGAAATGTGAAAGAATGAAAGGAAATGTCCTATTCTTCCAGGATTGAAGGGATATTTTGTTAGAAGGCACTAGTCTTGCCTCCAGGGGTACCAGTGATGGTTACACTGACAGGAATGGAACTCTTCTGCCTCCTGCTTATGAATTACAACCTCCTTGCAAGAGCCCTGTCTTGGGACTTCAAAGAAGCTCTTGTGGCAAGCTCAGATATGTACTATTCACTGTATTCTCTGATGGCTCAGTGTCATTCAAGTTTAAACACAAATATGTTGGAGGCACGAGCCTCCAAGTGTTTCTCTTCAGCAGCCTCTTGACTCCTACTGTCCTCCCTCCTCCCACAG
Seq C2 exon
GATGTCCTCTAGGGTTTTATGGAAAAGATTGTGCACTGATATGCCAATGTCAAAACGGAGCTGACTGCGACCACATTTCTGGGCAGTGTACTTGCCGCACTGGATTCATGGGACGGCACTGTGAGCAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000145794-MEGF10:NM_032446:18
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:
NO
A:
NA
C2:
PF0005319=Laminin_EGF=PU(63.0=65.9)


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:
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