Special

HsaINT0169703 @ hg19

Intron Retention

Gene
ENSG00000184012 | TMPRSS2
Description
transmembrane protease, serine 2 [Source:HGNC Symbol;Acc:11876]
Coordinates
chr21:42836478-42839813:-
Coord C1 exon
chr21:42839661-42839813
Coord A exon
chr21:42838081-42839660
Coord C2 exon
chr21:42836478-42838080
Length
1580 bp
Sequences
Splice sites
5' ss Seq
AGGGTAACT
5' ss Score
5.8
3' ss Seq
TTTTTTTCCTATTTGAACAGGCA
3' ss Score
9.09
Exon sequences
Seq C1 exon
GGTGACAGTGGAGGGCCTCTGGTCACTTCGAAGAACAATATCTGGTGGCTGATAGGGGATACAAGCTGGGGTTCTGGCTGTGCCAAAGCTTACAGACCAGGAGTGTACGGGAATGTGATGGTATTCACGGACTGGATTTATCGACAAATGAGG
Seq A exon
GTAACTATCCTGTCCTCCTTCTGACTGTGTTCTCCGATTCCTCGAGCCAAAGCCAGACATCTGTTAGGCGTGGTTCTGCTGCTGGAAGCTGACTGGTGACCACTGGTCAGCATGAAGCAAACTCTGCTTCCTCCAGCCACAGCCCCATCCCCCCAGTGTCCACCCATTGCCCATTGCCTCTCACTGGCTTCACTTGCATATTTCCCCTGGTGTTTGGATGAAAAGCGCTGGGGCTCAGCTTGTGTGAAATTCCTTGGTGCTCTGCCAACCACACTTCGTTCTGGCTCAGCTGACTCAGCTGTTCCACCCAGGCCACCTCACATCAAACTTTTTTTTTTTTTTTTTGAGATGGAGTCTCACTGTGTCGCCCAGGCTGGAGTGCAGTGGCACAATCTCGACTCACTGCAACCTTTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGCGCCACCACGCCCAGCTACTTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCGAAGCCCTGACCTCAGGTGATTCACCCACCTCAGCCTCCCACAGTGCTGGGATTACAAGTGTGAACCACGGTGCCCGGCCTCACATGAAACTTTTGATTTATAGAGAGCAGAGGGAAGAGCCGGCTGTGCCCATCCTTTTCTGGGGCCATCGAGTGGCTCCTGGGCAGCCCCCAAGGTTAGGAAGGGCAGGAGCAGCCAGGGTTCTCTGATGCCCCAGACTCAAGCACGAGGGAAGGTCTCAGGGGTTCCATGTGAGCCTCATGGATGTCTCTGCTTAGCAGAGCCCTGGCTTTGGGCATTGTCCAGATAGGGGGTGAGAACCAGATCTTCTCATCTCCAGGACCTCAGACGTATAGTTTTCTCAGATTTCTGTGCTTTCTGGGGCTGGGCTACTAGTGGAAGAAAGCAGTCTATTCTGTCTTCTCCCAAATCTCCCAGATGCCCAGTCTGTTGAAGGAGGAGCAGAACCAGGGGGCCTTTCCCGCTGAGGCCCGACCTGTGTCTCCTTCAAATGACACGCGGGACTCAGGGCCTTCCCATGACCATGGGGCCCAGGGGGCGTCACCTGGCCCAGGGCCCAGTGCTAGAAACAGATGACCCCAGGAGGAGGAGGCAGGGCAGGAGGGAAGCTGGCAGGGCTGGGATGGTCAGCCAGGCTGAGGGGCGGACTCGCACCAGGATGGAGCTAGGAAATGATCCAGGTGTGTTTGGCGGCTGCAGGTGGGTCCGCATGGCTGTGCAGGGAGGGAAGGGCTGCGTGGCAGGAGAGCAGCCGGGGGAGGCCCAGACTCTGCTGAAGAGATGCCTGTTGTGCCGGCCTCCACATCCGCTGCCCGCTCCTTCCGGAGCTCCTGCCCCGCCATGCTCAGCCTGACTCTGACCAACACGTTGGAGAGAAGAATGATCCCTTTGTGCTATTAAGCTTGCTTATTTGGTTTCTAAGTGCTTCATGCGAACCTAGAGGAAAAAATTATTTTCCACCTTTGTTTGTCTTAAGAAAATAACACACTTTTTTTTTTCCTATTTGAACAG
Seq C2 exon
GCAGACGGCTAATCCACATGGTCTTCGTCCTTGACGTCGTTTTACAAGAAAACAATGGGGCTGGTTTTGCTTCCCCGTGCATGATTTACTCTTAGAGATGATTCAGAGGTCACTTCATTTTTATTAAACAGTGAACTTGTCTGGCTTTGGCACTCTCTGCCATTCTGTGCAGGCTGCAGTGGCTCCCCTGCCCAGCCTGCTCTCCCTAACCCCTTGTCCGCAAGGGGTGATGGCCGGCTGGTTGTGGGCACTGGCGGTCAAGTGTGGAGGAGAGGGGTGGAGGCTGCCCCATTGAGATCTTCCTGCTGAGTCCTTTCCAGGGGCCAATTTTGGATGAGCATGGAGCTGTCACCTCTCAGCTGCTGGATGACTTGAGATGAAAAAGGAGAGACATGGAAAGGGAGACAGCCAGGTGGCACCTGCAGCGGCTGCCCTCTGGGGCCACTTGGTAGTGTCCCCAGCCTACCTCTCCACAAGGGGATTTTGCTGATGGGTTCTTAGAGCCTTAGCAGCCCTGGATGGTGGCCAGAAATAAAGGGACCAGCCCTTCATGGGTGGTGACGTGGTAGTCACTTGTAAGGGGAACAGAAACATTTTTGTTCTTATGGGGTGAGAATATAGACAGTGCCCTTGGTGCGAGGGAAGCAATTGAAAAGGAACTTGCCCTGAGCACTCCTGGTGCAGGTCTCCACCTGCACATTGGGTGGGGCTCCTGGGAGGGAGACTCAGCCTTCCTCCTCATCCTCCCTGACCCTGCTCCTAGCACCCTGGAGAGTGCACATGCCCCTTGGTCCTGGCAGGGCGCCAAGTCTGGCACCATGTTGGCCTCTTCAGGCCTGCTAGTCACTGGAAATTGAGGTCCATGGGGGAAATCAAGGATGCTCAGTTTAAGGTACACTGTTTCCATGTTATGTTTCTACACATTGCTACCTCAGTGCTCCTGGAAACTTAGCTTTTGATGTCTCCAAGTAGTCCACCTTCATTTAACTCTTTGAAACTGTATCATCTTTGCCAAGTAAGAGTGGTGGCCTATTTCAGCTGCTTTGACAAAATGACTGGCTCCTGACTTAACGTTCTATAAATGAATGTGCTGAAGCAAAGTGCCCATGGTGGCGGCGAAGAAGAGAAAGATGTGTTTTGTTTTGGACTCTCTGTGGTCCCTTCCAATGCTGTGGGTTTCCAACCAGGGGAAGGGTCCCTTTTGCATTGCCAAGTGCCATAACCATGAGCACTACTCTACCATGGTTCTGCCTCCTGGCCAAGCAGGCTGGTTTGCAAGAATGAAATGAATGATTCTACAGCTAGGACTTAACCTTGAAATGGAAAGTCATGCAATCCCATTTGCAGGATCTGTCTGTGCACATGCCTCTGTAGAGAGCAGCATTCCCAGGGACCTTGGAAACAGTTGGCACTGTAAGGTGCTTGCTCCCCAAGACACATCCTAAAAGGTGTTGTAATGGTGAAAACGTCTTCCTTCTTTATTGCCCCTTCTTATTTATGTGAACAACTGTTTGTCTTTTTTTGTATCTTTTTTAAACTGTAAAGTTCAATTGTGAAAATGAATATCATGCAAATAAATTATGCAATTTTTTTTTCAAAGTAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000184012-TMPRSS2:NM_001135099:13
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0008921=Trypsin=PD(19.7=88.2)
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:
GGCCTCTGGTCACTTCGAAGA
R:
GACAAGGGGTTAGGGAGAGCA
Band lengths:
358-1938
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains