Special

HsaINT0149199 @ hg19

Intron Retention

Gene
ENSG00000095370 | SH2D3C
Description
SH2 domain containing 3C [Source:HGNC Symbol;Acc:16884]
Coordinates
chr9:130506843-130509550:-
Coord C1 exon
chr9:130509426-130509550
Coord A exon
chr9:130507379-130509425
Coord C2 exon
chr9:130506843-130507378
Length
2047 bp
Sequences
Splice sites
5' ss Seq
CTGGTATGG
5' ss Score
7.13
3' ss Seq
CTCTCTCTACCTTTCTGCAGTAA
3' ss Score
8.32
Exon sequences
Seq C1 exon
TACGTCGCTGCCCCGCCCTCGGGACTCCATCCGCAGCTGTGCCCTCAGCATGGACCAGATCCCAGACCTGCACTCACCCATGTCGCCCATCTCCGAGAGCCCTAGCTCCCCTGCCTACAGCACTG
Seq A exon
GTATGGCCAGCAGAGGGGGTGGAGCAGGTGGAGGGAATCTGTTGTTGAAGACTTCTGTCACCTATGTGTGGTTATGTGTGTTTCCGCCTCTTTTATGAGGCGCGACCTTTACCAAGAGAAAGAACTGACACTGGAATCCTGCTAACAGAACTGTTGATATCAACATATAAGATGTATCCATGGTTTGTTTATTTAGCAACTATTTATTTGTTTTTGTGACAGTTTTGCTCTTGTGGGCTGGAGTGCAGTGGTGGGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCTTGCTTCAGCCTCCCAAGTAGCTGGGATTACAGACCCCTGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGTGTTTCGTCATGTTGGCCAGAGTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCACAGTGCTGGGATTACAGGCGTGTGCCACCATGCCTAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGGTGGTCTCGAACTCCTGACCTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCTGGCCTCTATTTTTCTTAATAGACTTTATTTTTTAGAGCAGTTTTAGGTTTGCAGCAAAATTAAGTGGAAAGTACGGAACACTGTGCTTTCTTATAAATACGAAGAAAGTTTCTCTGTTAGAAACATTCCAATAGATCATTTCTGGAAAAAAAATAAAAAGAATGTTTTCAACAGGCCGTATTGTCCACGTGGCAGGCCAAGTGTCACGAGAGGGGGCTGACTCAGGAGGAACTTTCGCCTAGGGTGGCATTCCATTGAAGTGTTGCTGTCTGTATCGGTTGTCACAAATCCTTCCCTAAACACAGAGCCACCAACTTTGTCATAACTACAAACTTGATTTCAAAGCAATACCCTGAGTATAAAACCTAAAATTCCTTGCCAGAATGACTTATTGGACAGTTTCTAAGCAATCTGGTATAGTAAAGCAGCCCAGATGTCAAGACTTAAATCTCAGCTGTACCACTTGCTGGCTGGGTGACCTTGGGCAGGTTAGTGCACCTCTCTGAGCTTCACTTTTCTCATCTGTAGAATGAGGATTATAAAAGTACTTACTTCATAGGACATTGAAAGGATTAAATAGACTGAGGTACAAAGAAGGGTCTTGCAGGCACTAAGAGCTTAGTAAATATCGCCTTTGAGGTTTGATGATGGTTTTACTGTCATTATGTCTCCAGCATGTTGCCAGCTCCTAGCACACAAGGTTTAGCAACAAATCATTATTGCTAATTCAGGCCGGGCATGGTGGGGCACATCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACAAGAATTGCTTGAACCTGGGAGGCGGGGGTTGCAGTGAGCTGAGATCATGCCATTGCACTCCAGCCTAGGCAACAGAGCGAGACTCTGACTCAAAAAAAAGTTAGCCAGGCGTTGTGGCACATGACTGTAATCCCAGCTACTCGGGAGGCTGAGGCTCAAGAATTGAAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCTAGATGGCACCACTGCACTCCAGCCTGGGCCACAGAGCGAGACAGTGACTCAAAAAAAAAAAAAAAAAAAAAAAAAAGGAAATCATTATTGCTAATTCGTCGAGAAACAATCACATGTGGCACAAGAAACTCCAGCAGGTACTCAGCTTCCCCGGATCACTGAAGCTCCTCCAAGCAGTGGGTCCCCAAGGCTGCAGCAGCCTCAGGGTGGGGCCATGCAAACTCCTGGGTCCTGGTGATTTCAGAGCATCACCTGGGCTGGTCAGCTTGCCAGAGTCAATCGGCCCTGGTCTCTGGTGATGCAGGGAGGTGGGGACATCACCTCTGTACTCCCTACAAGGAGTGAGGGAGCCTGTTCTTTGGGAAGGGGTGCGGGAATCTCACTTTGGTGGGGAGCTGCTATAACGGGGCCTCTCTCTCTACCTTTCTGCAG
Seq C2 exon
TAACCCGTGTCCATGCCGCCCCTGCAGCCCCTTCTGCCACAGCATTGCCTGCCTCCCCTGTCGCCCGCCGTTCCAGTGAGCCCCAGCTGTGTCCCGGAAGTGCCCCAAAGACCCATGGGGAGTCAGACAAGGGCCCCCACACCAGCCCCTCCCACACCCTTGGCAAGGCCTCCCCGTCACCATCACTCAGCAGCTACAGTGACCCGGACTCTGGCCACTACTGCCAGCTCCAGCCTCCCGTGCGTGGCAGCCGAGAGTGGGCAGCGACTGAGACCTCCAGCCAGCAGGCCAGGAGCTATGGGGAGAGGCTAAAGGAACTGTCAGAAAATGGGGCCCCTGAAGGGGACTGGGGCAAGACCTTCACAGTCCCCATCGTGGAAGTCACTTCTTCCTTCAACCCGGCCACCTTCCAGTCACTACTGATCCCCAGGGATAACCGGCCACTGGAGGTGGGCCTTCTGCGCAAGGTCAAGGAGCTGCTGGCAGAAGTGGATGCCCGGACGCTGGCCCGGCATGTCACCAAGGTGGACTGCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000095370-SH2D3C:NM_001142531:5
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=0.649
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0061714=RasGEF=PU(11.3=9.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
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