Special

HsaINT0147512 @ hg19

Intron Retention

Gene
ENSG00000137872 | SEMA6D
Description
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D [Source:HGNC Symbol;Acc:16770]
Coordinates
chr15:48056835-48057253:+
Coord C1 exon
chr15:48056835-48056990
Coord A exon
chr15:48056991-48057079
Coord C2 exon
chr15:48057080-48057253
Length
89 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGA
5' ss Score
9.22
3' ss Seq
TGTGCCGCCTCCTCTTGTAGGTA
3' ss Score
11.87
Exon sequences
Seq C1 exon
GCCTGGCTGTTGTGCAAAACACGGCCTTGCCGAAGCTTATAAAACCTCCATCGATTTCCCGGATGAAACTCTGTCATTCATCAAATCTCATCCCCTGATGGACTCTGCCGTTCCACCCATTGCCGATGAGCCCTGGTTCACAAAGACTCGGGTCAG
Seq A exon
GTGAGATTGTGTGTGAAACACTCCTTCCTATTCAACGTTTTCTCTGCCCGTTGGCCTCCCCTTCTGATCTGTGCCGCCTCCTCTTGTAG
Seq C2 exon
GTACAGACTGACGGCCATCTCAGTGGACCATTCAGCCGGACCCTACCAGAACTACACAGTCATCTTTGTTGGCTCTGAAGCTGGCATGGTACTTAAAGTTCTGGCAAAGACCAGTCCTTTCTCTTTGAACGACAGCGTATTACTGGAAGAGATTGAAGCCTACAACCATGCAAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137872-SEMA6D:NM_153619:12
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

In the CDS, with uncertain impact

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

C1:
PF0140314=Sema=FE(12.2=100)
A:
NA
C2:
PF0140314=Sema=PD(13.8=96.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACCTCCATCGATTTCCCGGAT
R:
TGTAGTTCTGGTAGGGTCCGG
Band lengths:
169-258
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