Special

HsaINT0101846 @ hg19

Intron Retention

Gene
Description
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:3232]
Coordinates
chr1:3428570-3431236:-
Coord C1 exon
chr1:3431114-3431236
Coord A exon
chr1:3428693-3431113
Coord C2 exon
chr1:3428570-3428692
Length
2421 bp
Sequences
Splice sites
5' ss Seq
AAGGTAGGA
5' ss Score
9.45
3' ss Seq
CTGTGGTCTCTCCCCTCCAGATG
3' ss Score
12.23
Exon sequences
Seq C1 exon
GTAGAAGCCCGTGTGCCAACAGGAACGGCAGCTGCATGCACAGGTGCCAGGTGGTCCGGGGCCTCGCCCGCTGTGAGTGCCACGTGGGCTATCAGCTAGCAGCGGACGGCAAGGCCTGTGAAG
Seq A exon
GTAGGACGCCCCTCCCCTGCTCCGCCCCGCCCAGGGTCAGAAAGCGCACCCAGGTGCTGTGGAGGGACCCGTGTCTAACTCTGGGGCCGTGGCCTCCCATGAGACCAGGCCCTTTGGCCTTGCCCCCTTGGGTGACCTGGGATGTGGCGGTCTCATCTCCCTTGCTGGGGGCTGAGGGGCGAGGGTAGGAAGGCTCGCAAAAGCTGCTCCCAGCCCGAGGCTCATTTCACTAGGAGTGAGCCAGGGAGCCCAGGTGTTGCTTATAGTTTTTAAACTATTGTATTTCCTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTATTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAAGCTCCGCCTCCCAGGCTCACGCCATTCTCTTGCCTTGGCCTCCCCAGCAGCTGGGACTACAGGCACCCGCCGCCAGGCCTGGCTAATTTTTCGTATTTTTAGAAGAGATGGGGTTTCACCATGTTGGCCAGGATGCTCTCAATCTCCTGACCTTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCTGGCCTAAACTATTGTATTTCCTAAGTAGTGCCTGCCCAGCAGGAAAACTGAAGAGATGAATAAGAGAAAAGGAGAAATGAGCCAGGCGCTGTGGCTCACACCTGTAATCCCAGCACTTTGGTAGGCCAACGAGGGAGGACCACTTAAGCCAAGTTGCTCAAGACCAGCCTAGGCAGCATGGCGAGACCCTGTCTCTAAACAATTTTTTTTTTAATTAGCCAGGTGTGGTGGTGCTGTCTGGAGTCCTAGCTACTCCGGAATCTGAGGCAGGAAGATCACTTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCTATGATCACACCACTGCACTCCAGCCTGGGTGGCAGAGCAAGATTCTGTCTCTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCCAAGGTGGGCAGATCACTTGAGTTTAGGAGTTCAAGACCAGCCTGGGCAACATAGCGAGATCCTGTATGTACAAAAAAATAAGAAAACCCAACTAGCTGAGCATGATGGTGCACACCTGTGGTCCCAGCTACTCAGGAGGCCGAGGCAGGAGTCCCAGCTACTCGGGATGCCGAGGCAGGAGTCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATCACTTGAGCCCAGGAGGTTGACGCTACAGTGAGCCATGATTGCACCAGTGTGCTACAGCCTGGGTGACAGAATGAGACCCTGTCTAAAAATAAATAAATAAATAAATAAACAAGTAAAATAATAAAAAAAATAGAACTCAAGAAGAAAGGAGACATTGTTCCTGAGCCCAGGAAACACCTAGACGTATGGGATGGGCTGCTTCTGCTGCTTCACTGGGGCTGTTTGTGAATGTGCTTGCTTAGAGTCAGGTTGCAGGCAGGTGCCATTGTTTGGAACACACCGCTGCCCCCTCTGCCACACCACACCATCCTCTGCAGCATGGCTGGGCGACGTTTATTTGTTAACCCTGTCCCTGCACGTCTGGGTGTTCCTGACTCTTCCCTGGGCCAAGCAGCCTTGGGGAGGGGTCGGGCTGCCACTGCCCCAGTGGTCCACAGGGTGAGTCTCTGAGGCAGCGGTGTGTGTCCAGACCAGGCAGTGGTCAGTTTCCAATGGTATTAGTCCATTTTCACGCTGCCGATAAAGACATACCCAAGACTGGGCAATTTACTAAAGAAAGAGGTTTAATGGACTTACAGTTCCACATGGCTTGGGGCGGCCTCACAATCATGGCGGGAGGCCAGGAGGAGCAAGTCACACCTCACGTCGATAGCGGTAGGAAAAGAGAGGGCTTGTGCAGGGAAACTCCCGTTTTTAAAACCATCAGATCTCATGAGACTTACTCACTATCATGAGAACAGCACAGGAAAGACCCACCCCCATGATTCAATCACCTCCCACCGGGCTCCTCCCACCACACGTGGGAACTGTGGGAGTTACAGTTCAAGGTGAGATTTGGGTGGGGACACAGCCAGACCATATCATCAGGCCCCCGCCGGATGGCCACGGGGTGTCGTGGTGTGTGGTTCCACGTCCTCACTGACACCAGGAAAGTGCTGCCTGGGCACTGGCACCTGGTCATGCAACAGGCTTAGTGTGAGACCTGTGTGGGTGCCAACTTCTTCATCCCAGGGGACCTGCAGGGCTGTGACTAGTGGCCGTCAGGGACAGTGGGATTGGCCTTGAATGCCTGTGTCATGCGGCCACAGGCCCTGGGTGTCAGCAGGCCGTGCACTGTCTTCCACTGGTCCCATGCAAAGGCCCTTCCTGGCACCTCTGAGCCCTCCCTGTGGTCTCTCCCCTCCAG
Seq C2 exon
ATGTGGACGAATGTGCCGCAGGGCTGGCCCAGTGTGCCCATGGCTGCCTCAACACCCAGGGGTCCTTCAAGTGCGTGTGTCACGCGGGCTATGAGCTGGGCGCCGATGGCCGGCAGTGCTACC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162591-MEGF6:NM_001409:7
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:
PF146701=FXa_inhibition=WD(100=85.7),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
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

  • Autistic and control brains
  • Pre-implantation embryo development