Special

HsaINT0147363 @ hg38

Intron Retention

Gene
ENSG00000187764 | SEMA4D
Description
semaphorin 4D [Source:HGNC Symbol;Acc:HGNC:10732]
Coordinates
chr9:89388872-89391415:-
Coord C1 exon
chr9:89391264-89391415
Coord A exon
chr9:89389048-89391263
Coord C2 exon
chr9:89388872-89389047
Length
2216 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGT
5' ss Score
10.47
3' ss Seq
TCTTCTTGTTGGGGTTTTAGGGG
3' ss Score
7.28
Exon sequences
Seq C1 exon
AGCCTAGTTTCGTGTTTGCTGACGTGATCCGAAAAAGCCCAGACAGCCCCGACGGCGAGGATGACAGGGTCTACTTCTTCTTCACGGAGGTGTCTGTGGAGTATGAGTTTGTGTTCAGGGTGCTGATCCCACGGATAGCAAGAGTGTGCAAG
Seq A exon
GTGAGTGCCAGGCACTCTGGCTTCGCTTGGCCCCTGCCATGGCAATAGTGTGCCTGGATGATGGGTGGCTCCTGACCTTCGTCTCAAATGTCACTTTCCCTAGCACTTTATTCCCTTGGGCCTCAGATGCAGCTCTCAATGGATCTTATTTCTGGGGGTTGTGGGGACTGAGGGAGTGCTGGCCCCCATGTGTGACCCATTAGCCTCCTCTTCTCAGGAGGTTCTTTCTTTTAATGCACCCTCTTCAAACCTCTAGCTTATAAAAAGCAAGGCTTTGTGGAATGTATTCACCAGAGTCTGTTGGAATTTCACCATTTGGCTCTTAATCTACCTAAGAGTGAAACATTAACCGACAGCTTAAGATTAAGAAGAGAGAACCAATACAGAAGTTTGTCAAAACACAAATCTTTAAGTACATTAAAAGGGGAGGGTGCCTTTAAAATGACACACTGTAGGCACAGTGCTCAGCACAAGAGAATGGCCTATGGGCTTGATTACAGGAAATCTCAAGGTTGCTCAGTGGCAGTTTCCAGGAGGTGGATTGTCAGGCCTCAGGGGAGCTGGGGGAAACCACATGAAACACAGCCGCCATGTCCCTGGCCAGGAGCTCATCTCGGAGCAGGTAGCCATTCGTCTCTCATGGAAATTGGTAGATAGTTCTTGCGTGGCCCTTTCTCATGTAGTCATGACCATCAGGACATCAGAGAAGCAGGGTTCCTTTCATGCCTATGGCGCACAAAAGTGGGTGCCTTTGACACCGTTCCCTTAACAGCCCCTTGCATAAGGAAGAAGGTTGGGTGATGTGCACACCTGAGTATCCACCTGGTGCTTTGCTCCCTGCCCAGGCCTTCCGTAGCCAGGGCTCACTGACCAGATCCTCCAGCTGCCCCGCAGCCCCGCAGCCGTGGCTGCCATGCTCCTGTCTTGCAGACCAGGAAACCATCCTATCAACAGTATCAGTGTTGGGGGCAAGCCAGTGCCCCTTGAGATGGGGAGGGTGCTGCAGGGCCAGAGCTCCTGGCAGGCGTGCACAGTGCTCAGAATGCTGTCAGAGCAGCACTGGCCAGGGGACTCGAGCCCTCCCCTGCCATCGGGAAGCCAAGGATCAGACTTGCCTTGACCTTGACTTATTACCCAGCACTGAGGGTTTGCAGCAGGATCAGTGAGCAGATTCAGCGATGCACAGAGCAGCCACCTCCACCCCCGACAAGTTTCTACAAGTCTTAGGCACACTGCTGTCATCCCCTCTGATCCCTTTTTTTTCCCCATACTTGTTTGAACTCCTGGACTAGGGTGGTTTGAGCTTAGGCCCCACAGCTCCTGCCTACCACGCAGGCACACATGAACCCTTCACCTGCTGCCCGTGACCTGAAAGCCACATGAGACCCCTGACGAAAAATGTGCTAGAAATTATTCTTTGCTAAAACATCAAGGAGGAAAATGAAGTCCTTTTATCAAAAAGAGAATTTGGGCTCCTGTAATCACACAGCAGAGATGAAGGGGGAACATTTTCCCTGTGTCCAAAATAAGTAAGGCTGCTTCTATTTCATATTCTTCTGCACTCAGGTTTTGTGGTTTCAGTATTTCTCTCCAGACCACACACAGTCATGTGTAGTTTATAATTGTGTCTTGGTCATCGGATCCCTGAAAAGCGTTTATAAAGAACTTAGGTTCAAAGCACTTTAGCAGATACTTTGGGTAGAAAGGAAGTGAAGGATCTATTCCTTTAAAGGGAGGAAGGTTCACACATTTGCCCAAGACAGGCTGCAGGGCCGGTGGCTGTCCCCTGGAAGGAGGCTGCCGCCACTTGCCCCACCCAGAGCATGTTCATTGATGGGCCCTATGTCAGGAAAGTCACACAATGCCAGGGGCCTTGGCAGTTGGAAGTGTGTGAGCACGGCAGCACCTCTGCGGTTGCAGGACTGAATGCTGGGCACAGGCAGGCATGGACGATCAAATGAGCTTTCAGTGAGAGGGCTTTTGTCCGTTTTGTTTTGTGTGTTAACCCAGGAGCGTTCTGGGATCCAAGCTGGAACCTGGACGTGGTGCTGCGGGCCACTCACATAATTGCGGCATCTGTCTCCTGTTGCCCGAGCTTTGTTTCAGTCAGGCACAGCCGCGCTGTGCTGGGCCATGGAGGGGTGCACCTCTGACCTTAGTGCTTGCTCACAGGGGATCCACTCTCGGCCCACCACGTCTTCTTGTTGGGGTTTTAG
Seq C2 exon
GGGGACCAGGGCGGCCTGAGGACCTTGCAGAAGAAATGGACCTCCTTCCTGAAAGCCCGACTCATCTGCTCCCGGCCAGACAGCGGCTTGGTCTTCAATGTGCTGCGGGATGTCTTCGTGCTCAGGTCCCCGGGCCTGAAGGTGCCTGTGTTCTATGCACTCTTCACCCCACAGCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000187764:ENST00000455551:10
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=0.000
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(11.5=100)
A:
NA
C2:
PF0140314=Sema=FE(13.4=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
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

  • Autistic and control brains
  • Pre-implantation embryo development