Special

HsaINT0147379 @ hg19

Intron Retention

Gene
ENSG00000187764 | SEMA4D
Description
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D [Source:HGNC Symbol;Acc:10732]
Coordinates
chr9:92008477-92011750:-
Coord C1 exon
chr9:92011652-92011750
Coord A exon
chr9:92008571-92011651
Coord C2 exon
chr9:92008477-92008570
Length
3081 bp
Sequences
Splice sites
5' ss Seq
CTGGTAAGG
5' ss Score
9.68
3' ss Seq
CTCTTTTTATTCAATTGTAGAAC
3' ss Score
9.67
Exon sequences
Seq C1 exon
ACAGAGTGCCTCAACTACATCCGGGTGCTGCAGCCACTCAGCGCCACTTCCCTTTACGTGTGTGGGACCAACGCATTCCAGCCGGCCTGTGACCACCTG
Seq A exon
GTAAGGCTGATGGGCACCTCCCTGTGCTCACGCCAGCCTGGTCAGCAGTTAAAGTAGAAGGGGGCTCAAAGCAGACGTAAAGCTGTCTCCACCCTAAAAAAAAATAGGATTTTCTCAGAGCCAGCTGCAGAAAACGGGGGCAGCTTGTGGCCCCTCTGAAAGTCTTGCACAGCTGCTGTCAGGGGCACACAGCCCACTTGGCTCCTCTAAGTTTCGGTGTCCATGGCCAAGGGTGAGGCCTGGGGTGCAGCTCAAGGTGCTGGGAGCCCTTGGTGCTAGTGCAGAGCATGCCATGGAGGGGCGTGCTGGAAAGTACAGACAGCCTGAACATGGCATTGGGGATGTGCTGGGAAGGACAGGTAGCCTGAACATGCTATGGGGTGAGGGGACGTGCTGGAAAGGACAGACAGCCTGGCAGCTCTGGGCATCTGGGTCAGGTGGAAAAGTCAGGACTTGCTCCTGGCTTGTGTGTTCTTGGTTGGTGCATCTGTGCTCTGGCTGTGGGACCCACCCTTCTGGTCGGCTGTGGTGTGCAGCTTGCTCACTGAACCACTCCTGGGTCCACCCACTCAGGGGCAGCAGGTCAAGTGTGCTGAGCACCTTGAGAAGCAAGTCCGGCCTCTGTCCCTCACCGGCTCACATCCTTGACTGCCCAGCCTGGTATCCGGCACCTCCCCCTGTGTGACGGTCCTTTCTATCCAGATAATCTGATGAGCAATGTGATGATCATCAGAGAGGGAGAAGTAGCATTTTAAATAAGTCCATGTGAACATGGAAAATGAAGCACATTTTCTACTGTGTATCCCTGGATTTTAATGAGTCCTGATAAATGTAAAATATGCCACAGTGAAAAGCATCATTTGCTAGAACCCTAAATTAATTGGAATTAAAATATTTTCCAATCTTGAGTCAGAGATAAATGACAAGACAACGTATGGCCTCATTAGAGACTTGATGAGGAAGCCTGGTATTTGCACACAGACGTCTGGGGTGAGATTCATAGTAGGGGTCTACCCAGCTGCCTGTACCACAGATGCTGGCAACGAAACCTGATAGGGGGTGGGGGTGCTTTGGGGATAGTAAGACCCTCAGTCCTCAAAGACAGTCGTTTGTATTTACTTTTGTGCAGAAAGTACGGTTGGACCAGAAACATTTTGCACAACAAAGGATTTTTCTGGCTAAACTCAATCAGAAGCTTAAAGTTCTGTCATTTAAACTTACATTCTGTAGATAGGTTAGCTGTTGAGGTTAGAGGATACTGTATTTGGTTTAAATTTAGACCTATAATTTTTCCTAATTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTACAGTGATGCGATCTCGGCTCACTGCAACCTCCATCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGATTACAGGCATGTGCCACCACGTCTGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCTGAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGTATTACAGGCATGAGCCACCACGCCCCGTCAATTTTTCCTAATATTTTTAATAAAAGTTTTCACAGCTGCAGAAAAGATGTATCACTTGTATATCCTGGCAACCTAGATTGCACAATTGGGAGTGTGTGTGTGCACGTGTCTGTGTGCCTGTGCATGTCTATGTGTCCACATGTGTGTCTGTGTACATATGTGTGCTTGCTGAACTATGACCCGTGACTCCCAAATGCCTTCACAGGCATCTCCTAAGAATAGTAACATTTTCCTATGTAACTTCAGTTTTATCATTATATCTAAGAAAACGTTCAATCATTCCCCAGCATCATCCAGTCTCCAGTCCCCGTTCAGATTTCCCCAACAGCCCCGAAACCTCCTTTCAAGGTATGCTAAATGGTCACATCCAGTGGGGTTCACATTCCCTAACCTAACAGGTGAAGAGCTGTGTGCTGCTTTAACTGGCCTTTCAAGGGTGTCAGCTGCGGCCTTCCACGTGGTCTGAGCCTTCCTGCTCTGCTTCCGAGAGCGTGTTTCCAGCCAGCCTCCTGCAGCAGAGGTGCTGGGTGCCCTTGCCCCGCCGTGGGCCCTGCCTGTCTTCAGCATGCCCAGGCTGTTGGCTGCAAAGTGGCATCCCCACGCGTGTTCTGTGTGCTCTCTGGTTCCCGGCAGGCTCAGCCCCTCTCTCGTCTGTGCTGTCCAGATGGGTTTCTTCTGTCACTTGCTGGATTTTGCCTGTTTTTCTCCTGGATGCCCTTTCTCACTCGTTTGTCCACACTTCTCACATGTTCAGGGATGGAGACACCTCATCTGCCATTCTGTAGGCATTTCCCCCAGTTTGTCACATATTTAACCTTGCCGTATTATTTCCCCATGTGGAACTTTCCAGTTCTCTCTGTGGTTGGATCTGTGCATTGTTTTCCTCATGTGGCTGTGGGCACTCTGGCCAGGTAAAGAGAGGACCCCCAGATGGAAACGCCAGCCCCTGCTCTGTTTTAGTACAGTGCGGTTCTGTTTTTAGTATTCAGATGGTTGATCCATCTGGAGTGTGTTTTGGTGGGTGGAGCGACGTAGAGATTCTGCCTGTTTATGTTTTTCTGCTTCCTATTTATTGGGTCACCTAGCTGCTTAGAATGCCGTCTTTATTGATGTTAAAATTCTGCTCATGGGCTTCCGATTACATACTGAGCACGTCCTGTGTTGGGTTTATCCTGGTGGCTTTCCAGCCCTAGAGCCATCAGCGTTGCCATTTCCATTTTGCAGATGAGTAAATTGAGGGTCTGAGATCTTGAGAAGCTTGGCCAGGGCAACGGAGCAAGGGCACCAAGGTGCTGATGTCTAGACCTGAGCTGAGCAACACAAGCCCTGGCCCTAGTGGGCGGGACTCCTGTAGCTCCACACCTATCTGCTCGGCCCTGTTGGTCTTCCGAGAAGAGCAAATTTGTAAAATGAAGTGGTACAGAGACACATTGTTACTATAGAAATTCAGCCATCTGATGATGTGCTCTCTTTTTATTCAATTGTAG
Seq C2 exon
AACTTAACATCCTTTAAGTTTCTGGGGAAAAATGAAGATGGCAAAGGAAGATGTCCCTTTGACCCAGCACACAGCTACACATCCGTCATGGTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000187764-SEMA4D:NM_001142287:8
Average complexity
IR-S
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(33.0=100)
A:
NA
C2:
PF0140314=Sema=FE(7.2=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