Special

HsaINT0104639 @ hg19

Intron Retention

Gene
ENSG00000196199 | MPHOSPH8
Description
M-phase phosphoprotein 8 [Source:HGNC Symbol;Acc:29810]
Coordinates
chr13:20233341-20235978:+
Coord C1 exon
chr13:20233341-20233429
Coord A exon
chr13:20233430-20235837
Coord C2 exon
chr13:20235838-20235978
Length
2408 bp
Sequences
Splice sites
5' ss Seq
GAGGTAATA
5' ss Score
7.96
3' ss Seq
TATTTAACAAACCAACACAGGAT
3' ss Score
2.12
Exon sequences
Seq C1 exon
ATGTGTTAAGGGATGCTGTGAAAAATGGGGATTATATTACTGTAAAAGTTGCACTTAATTCAAATGAAGAATATAACCTGGACCAAGAG
Seq A exon
GTAATATGTCGTTGAAAAATCTCATGAAAGGAAAATGGAAAGTAACACTTGAAAGAATTCAGTTTAACTTTTCATTTATTTTAATTACAAAAGGCTGGGCGTGGTGGTGCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGGATTGCTTGAGCCCAGGAATTCAAGACCAGCCTGGGCTCCATGGTGAAACCCCAACTCTACAAAAAATACAAAAATTAGCTGGACATGGTGGTGTACACCTTTGGTCCCAGTTACTTGGGTGGCTGAGGTGACAGGATCACCTGAGCCTGGGAGGTCAAGGCTGTGGTAAGTGGAGATCACACCACTGCACCCCAGCCTGGGCAACAGAGCAAGACTCCCATCTCAAAAAAAAAAAAAATAATGCACGTTCACTTTGTAAAATAAAAAAATTGTAGAACCCTATAAATGTACAATTATAGTCCCTTTAATTCCAACCCCCTCCCCTCTAAAAGTGATGGTTTGGTTTGGTTATGGTCTACCTGTTTTGTATGTGGTTTACCCTCTGCCACTCTTGAGAGCGTAGAGTGAGACCATTTTCCTGTGGTCATTTGTGTTTCTTTGATGGTTGTCCCATTTACAACAATGGTCCATCTCTCCTGTTGTAGCTGGGGATTTTTCATACTGATATGTATGGATTTTTTTTTTTTTTTTTTTTTTTTGAGACAGTGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGACTACAGTTGCCTGCCACCTCGCCCGGCTAATTTTTTGTATTTTTTTTTTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCTGCCTGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCCACGTATGGATTTTTTTAATGGAAGCATATTGACCCTTTCTCCCTAGATTTTAGGTTTGTGTTTGAGTCTTGTATTGCTTGAAGATTTTTAGTTTTAGGCAATCATATCTGTTGATCTTTTACATTTATGGCTTTTGGGTATCTTGTCTTGCTTAGAAAATATTTTTATATTCTTTAGTTTTTTAGCTTAGCTGTGGATTTTTTAGGTTTAATCCTTTGGGATTACAATTCACAAAATTATTGGGCTTTTGATTAAAATTGCATGAAATAATATAGATTGAGAATTGACATTTACTTTTTGCATCTTCTGTCTAGGAACATGGTAATTCTACATTCACTCAGCTCTTCATTTATATCCTTAAGCAAAGTTCTATGGGTTTTTTCATTCATATAGACGTTGCACATTTCCTATAGATGTATGCCTATATGTTTTATAATGGTCATTAGAGTCTTTTTTCATTTACATTTTGTTTTCTAACTGGTTATTGCTTGTCGATGGTAAAGCTGTGGATGTCTTTGTACACATAAGTGTGTGTAACTCCAGTCATTTAATGAAATTCTTATAGTTTTTAAGTTACTTGTTTTGGATTTTCTAGGTAGAAAATTTGATCGTATGCCCCCCAAAAATTCACTGTTCATTTTGTATGGTGCAAACTTTTCATGTGCCTTTAGGATTTAATACACAAAACAAAAAGAAGATACAAAAATGAGAGCTGGGCGTGGTGGCATGCACCTGTAATCCCATCTACTTGAGGCTGTGGCAGGAGGAATGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCTGACATAGCAACACCGTCTCAATAAAAAAGAAAGAAAGAAAAACAACACCAACAAAAAAAATTGAAGCATTCCTTGGAGATATTGTGGGTTTGGTTCCAGACTGTTGGAATAAAGCGAGTCACACAAATTTGTTGGTTTCCTGGTGCATATAAAATTTAGGTTTACACTATACTGTAGTCTAAATGTGAATAGCATTACATCTTTTAAAAAACCTATATATCTTAATTTACAACACTTTATTGCTAAAAAATGCTGACACAACAACACAAAATGAGCACATGCTGTGGGGTAATGATGTGAATAAACGTGCTTGTGGCAGGGTTACCACAAACCTTCCCTTTGTAAAAAACACAGTCCCTGTGAAGTGCAGTAAAGCAAAGCTCAGTGAAACAAGGTAGGCCTATAGAGGAAAGTTGTAAAATTTTATGCAAACATTCATATGTGAAAAGATACTCTAAAAGCTAGTAGCTTCTGATGGTTGGGATATTTTAGTGAAAATCCTAAGTAGATGCCTAAATCAGTGCCTATTAGTGATTTCACATTGAAACATCTCGAGTGAGAAGACTTGGTTCTGAAATTGTTCTGACTAAAGATTAACACGTTTTTTATTTAACAAACCAACACAG
Seq C2 exon
GATTCCAGTGGAATGACACTGGTGATGCTTGCCGCCGCCGGAGGGCAGGACGACCTCCTGCGACTCCTCATCACAAAAGGCGCGAAAGTGAACGGTCGGCAGAAGAACGGGACCACCGCCCTCATTCATGCTGCAGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000196199-MPHOSPH8:NM_017520:7
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.140 A=NA C2=0.249
Domain overlap (PFAM):

C1:
PF127962=Ank_2=PU(28.4=90.0)
A:
NA
C2:
PF127962=Ank_2=FE(48.4=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:


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