Special

HsaINT0169673 @ hg38

Intron Retention

Gene
ENSG00000137747 | TMPRSS13
Description
transmembrane protease, serine 13 [Source:HGNC Symbol;Acc:HGNC:29808]
Coordinates
chr11:117907454-117909968:-
Coord C1 exon
chr11:117909806-117909968
Coord A exon
chr11:117908785-117909805
Coord C2 exon
chr11:117907454-117908784
Length
1021 bp
Sequences
Splice sites
5' ss Seq
CGTGTAAGT
5' ss Score
8.58
3' ss Seq
CTCCTTTGTGGCTCTTGCAGGAC
3' ss Score
10.33
Exon sequences
Seq C1 exon
ACTGCGGACTGAGGGCCATGACCGGGCGGATCGTGGGAGGGGCGCTGGCCTCGGATAGCAAGTGGCCTTGGCAAGTGAGTCTGCACTTCGGCACCACCCACATCTGTGGAGGCACGCTCATTGACGCCCAGTGGGTGCTCACTGCCGCCCACTGCTTCTTCGT
Seq A exon
GTAAGTGCCTGAGAGGCAGGTGATTTGACACTGCCCAGGGTCGGGAACCACCAGGAAGGGCTGGCTGCAGACTGACTTCTTCGTGGAGGAGGATTCTGGGTGTGAGTCCAGCCCCCATGGGCCAGTTGGCACTGGTGTAGCTTGGGTGTTCACCTGGTCCTGAGAGTGTGGGTCGGGGGTGTTTGTTCCGAGCTAGGCCCAAGGATGAGAAAGTCCCATTGACGGCCCCAAGGGGGAGAGAGGCAGGCAGGAAGAGGGACTGGGAGCCTGCCCCTGAAGAACAGGGTGAAATGAAAAAGGCGTTGGGTTTGTTGCTGCTTCCTGCAAATGGAACTCATAGCAGAGGAGCCCCTAGTTATCCCAGAAATTGAGGGTTAGGGATTGCAGGCAGGGCACTGTATCAGCTGCTAACGGTCACCAGCTGGTCTATTGTCTTTGGGGGCCCACAGCCCAGGCTGGTGGGCAGGAAAGAGCTCTGGGACCAGGCCTCAGGGGCACTGGCCTCCCTAGTAATGAGTTCAGTGTGTTACTTTGTCCTGTCTGAATTTGCTGAGGGTAATAATACTGAGATCTTATCAGTACAAGCCCTTGACCCTGTCTGGTGAGTGAATCTGTGTCCCCATCCCTAGTCCCAGCACCTTCTGCAGCCCTGTGACTTGTCAGCATCTGTCAGTTCATATCGAGGCCCCAGAGTTTCAGCATGGCAGAAGTCAAAGTCTCCTATTTGATCCTTGGTGACTTGCAGAGGAGATAGTGGGGGGGGAGTGCCACACAGAGGTCTTACTCATCCTTCCCTCTTTATTACTGTAAGGTGCAGAGCTGCAAGCTCATAATTTTTGAGGGGCTGTGGGGGATTGCTTTGGACTCCAGGGATAAGATAGAGGGTTCCCTCCAGAGGTCATTTTATCCATCCTCCTGCCTCCAAGCTGGTGCTCTGACTGTGGCTCCCTGTAGGTAGCAGGGGCTGCCAGTGAACGCTGCCAGGCAGGTACTGGACCACGCTCCTTTGTGGCTCTTGCAG
Seq C2 exon
GACCCGGGAGAAGGTCCTGGAGGGCTGGAAGGTGTACGCGGGCACCAGCAACCTGCACCAGTTGCCTGAGGCAGCCTCCATTGCCGAGATCATCATCAACAGCAATTACACCGATGAGGAGGACGACTATGACATCGCCCTCATGCGGCTGTCCAAGCCCCTGACCCTGTCCGGTGAGGGAATCTGCACTCCCCGCTCTCCTGCCCCCCAGCCCCAGCACCCTCTGCAGCCCTCGCACTTGTCAGCATCTGTCAACTCATATCCGGGCCCCAAAGCTTCTGCAGGGCAGAAGTCAAAGACTCTTAAAGATCCTTACATGGAACACTTCTGTTTTATAATTAGGGAAACTGAAGCCCAAGGGTTATAAATAAGTTTGCTCCAAATGACACATCTCACATTACAAATTGATGACGGAGTCAGGGCTTGGGTACTGATCTTAATCAATAGATTGAATTCTTTCACTGGTATTAACTGAGCACCTAGGGGCCAAACGCTATGGTAGGCATTTCACACATATGATTTCATTTACTCTTCACAACCAACCCTGTGGAGCAGGCACTATTATTAACTTCATTTGACATATGAGGAAATGGAGCTTTACAGAGAGATAATTACCTGAGGCCACAAGTAATAGGTGGTAGCTCTGGGATTGGAACCAGGTCGATCTGATTCCCAAGCAGTGCTCTCCCCACCTGGCTCTAGACTGGCAAATTGCTTACCCTGCAGTCGAGAACTTAAGCTGAGTACACATTCAAACAACTAATTGCTACAACGTTGTTGCTAAGGACCAAAGGAGGCTACACAAAGGAAATGCTGCAGAGGTTCTCAGAAGATCACTGTGGACAGGGGACGTCAAAGAAGACTTCATTCATTCATTCATTCATTCACTCATCATTCATCCATTCACTCATTTGTTCACTTATCAAATACTATATGGCCAGCCCTATAGTACAGTTGCAAATAGAAATAAAATACACCAAGACGACCAGTAGAGGCCAATTATACGATGTTTTCGGGGAGCAGGGAGCTATGGTGGCATAGGCGGGAGCAACTAATCATCCTGGCAGGCTAGGGGAAGCTCAGCAGAGGAAGGATAGCCAAGGTGGGTCCCGAAAAGATTGGAGAAGACAGGTAATGGGGGCTCAGGGAGGACCCTGAAGAATGGAGCCAGAGCCCTCTGGCATAAGCATCTGTAAAGGTGGGAGAGGGAGGAGGAGTACCGGGATTTCTGGAAGCCTCGGAGGACTCTCTGGTTAGTCCAGCCATTCTCGTGCTCTGAGCCTGTGAGCTGGTGTTTCCTCGCACATTAATTATGGAGGCGGTGTCTATCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137747:ENST00000526090:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.184
Domain overlap (PFAM):

C1:
PF154941=SRCR_2=PD(5.5=9.1),PF0008921=Trypsin=PU(19.2=80.0)
A:
NA
C2:
PF0008921=Trypsin=PD(66.9=74.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CCTTGGCAAGTGAGTCTGCAC
R:
ACAGATGCTGACAAGTGCGAG
Band lengths:
350-1371
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains