Special

HsaINT0104630 @ hg38

Intron Retention

Gene
ENSG00000196199 | MPHOSPH8
Description
M-phase phosphoprotein 8 [Source:HGNC Symbol;Acc:HGNC:29810]
Coordinates
chr13:19666425-19668531:+
Coord C1 exon
chr13:19666425-19666579
Coord A exon
chr13:19666580-19668376
Coord C2 exon
chr13:19668377-19668531
Length
1797 bp
Sequences
Splice sites
5' ss Seq
GACGTAAGT
5' ss Score
10.93
3' ss Seq
GTACTATTTTTTTTTCTTAGACT
3' ss Score
8.33
Exon sequences
Seq C1 exon
GCCTGTAAAAGAGGAAATTCAGACATCGTACGACTCGTAATTGAATGTGGAGCTGACTGCAATATTTTGTCAAAGCACCAGAATAGTGCCCTGCACTTTGCGAAGCAGTCTAACAATGTGCTTGTGTACGACTTGCTGAAGAACCATTTAGAGAC
Seq A exon
GTAAGTGAGAAGCGACTGTGCCATAGTTAAGTCACATATCATACATCTGTTTATGTAGACATATTATAATTGGAGTGGCCTGTGTGTAACTGCTCAGAAAAACATCCAGCACAAGTCCTGATGGTTTTGTTTCCAGTAGATCACAGATTTAATAAATGGCATATGAATTATTTTTCTGCAAGTTATTTAACTCTCAGAAAATTTCAAACTTAACACTGGCCTATCTGGGAGTATTTTCCTTAAATATTAAGTATGCTCTTAATTTGGTTAGCAAAGGTTTTCTTAAAAACATTTAAACTTGGCCGGGCGCAGTGGCTCACGCTTGTAATCCTAGTACTTTGGGAGGCCGAGGCGGGTGGATCACTTAAGGTCAGGAGTTTGAGACCATCCTGGCCAACATGATGAAACCCTGGCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGTGGGTACCTGTAACCCCAGCTACTCAGGATGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGACCTGAGATCACACCACTGCACTCCAGCCTGGGCGACAGAGCAACACTCTGTTTCCGCCCCCCACCACCAAAAAAAGAAAGAAACTTTAAACATTTGTCTTTCTTTTTAATAGACTTTATTTTTTGCAACACTTTTAAGCACAGCAAAGTTGAGCGGAGGGTACAGATTTCCAAGCCTCCCCACCGCCATCCTCCCCGACTGTCGAGATCCCAGTCACCCACAGTGGGACATACAGCTGGGGAACCTACAGGGACATGGCATAATCCCCTGGAGCGCAGCATTGACATTAGGGCTCACTCGTAGTGTTACCCATTCTATGAATTTGGACAAATACATAATGACATCCATCCCTCATCACAGTGTCATACAGAATAGTTTCACTGCCTTAAAAAGCCTGTGTTTTCCACCTTTTCATCCCTCCCTCCCCCAGCCCCTGACAACCACCAGTAATTTAATTCCTTCATATTTTGCCCTTTCCAGAACAGGTGGAATCACACATTATTTGGTCTTTGCAGGTTGGCCTCTTTCATTTAGCAATAGGCATTCAAGATTCCTTCCATGTCTTGATAGTGCATTTCTGTTTAGCACTGACTAATATTCTGTTGTTGGTTGTCAAGATTTACTAGTTTATTCAAGTTCATTCTTTTTCAAATAAATTCTCAATCATATTTTATTTTATTGCAGGTTCATACTTATAACACAATTTAGTATTTCTATCACTTAAGAACTCTTGGCAACACATATCAGAAACTTGCATGTATCAGACAGTAGCGAACTCAAGGCGGTGTTTATGTAGCAGGTCTCGGGTGGGCCTCTGGGACCGCGCCTGTTGAACTCAGTGCTGCTGATGGCTGCAGTCCCAACTCCTCTGGTCACACGGGGGGTTTGCATAGATCCAGCAAGTAGAGTGACCCACTTTCCTGATTTGCCCAGTACTGAGGGGTTCCCCTTTCTGATTTTCCACTGATTCATTAGACAACTATGTATTAAGCATAGACTTTGTGCCAGGCACTGTTCTAAAGGCTGGGGAGATGGAAATGGCAGTGGAGGGAAGAGACTTGCCTTCTTAGAACTTCAATTCCACTGAGATGGACAACAAGACAGACACATGGGTGTCAGGTGCTTGGTGGAAGTAGAGCTGGAAAGCGGAGGCAGGCAGAGCTGCAGGTCTTTGTTTGGAAGGTTGGCCTGGGAAGCCCTCACTGGTATTCGACAGGCTTGTGGTTCTTTTCTACATTAACGTTAACACGTACTATTTTTTTTTCTTAG
Seq C2 exon
ACTTTCAAGAGTAGCAGAAGAGACAATAAAGGATTACTTTGAAGCTCGCCTTGCTCTGCTAGAACCAGTTTTTCCAATCGCATGTCATCGACTCTGTGAGGGTCCAGATTTTTCAACAGATTTCAATTACAAACCCCCACAGAACATACCAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000196199:ENST00000361479:10
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=0.005
Domain overlap (PFAM):

C1:
PF0002325=Ank=PD(72.7=46.2)
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:
GCCTGTAAAAGAGGAAATTCAGACA
R:
CTTCTGGTATGTTCTGTGGGGG
Band lengths:
310-2107
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