Special

HsaINT0075910 @ hg38

Intron Retention

Gene
Description
HGF activator [Source:HGNC Symbol;Acc:HGNC:4894]
Coordinates
chr4:3448128-3449495:+
Coord C1 exon
chr4:3448128-3448276
Coord A exon
chr4:3448277-3449236
Coord C2 exon
chr4:3449237-3449495
Length
960 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGC
5' ss Score
9.6
3' ss Seq
TGACCAACGTCTCTGCCCAGGGG
3' ss Score
6.21
Exon sequences
Seq C1 exon
ACGTGAGCGGCTACTCCAGCTCCCTGCGGGAGGCCCTGGTCCCCCTGGTCGCCGACCACAAGTGCAGCAGCCCTGAGGTCTACGGCGCCGACATCAGCCCCAACATGCTCTGTGCCGGCTACTTCGACTGCAAGTCCGACGCCTGCCAG
Seq A exon
GTGAGCTGGTGCCCGCCCCACCAGGACCCGACTGGTGGGGGCTCAGCTGGTCCTGAGTCTCCGAGATGCTTGCCCCTGGGGAGCCCAGAGCCTGGCGGCACCCCAACCTGGCAGGGCCAGCCAGGGACCCCTGGGCAGGGAGCACACTTACTGTCGGTGGCCAGCACCCCAGGGCCACCCAGAGCCCTGCCGGAAGGGCATCCTCCTCACACAGAAGGGGAGACCCAGGCTCTGAGAGGGGCCTGGGGTCCCACAGAGCCCGGACAGTTCCTGGCTGTCCAGCCCAAGGCAGTGCTTTCCGTGTGACACTAGGCACCAAAGGCCCCTTTGCCCCGAGTTCTCTCAAGCCAGCTCTTCAACCTTCAATAAGTTCTTCAACCTTCAATAAGCCCAACAGCCCAACCACGTCCTGGGCTCTGCAGGCCTGTGTGCTCAGGCGGCACGGCAACCCTGGCATGCGACGGCTCTCTTATGCCCCATTTTATAGCTGGGGAGACTGAGCCCCAGGCAGTCAATTCACTCTTCCAAGGCCACAAAGCCCAGGAGTGGTAGAGTGGGTAGGGCTTGTCACTGGACCTCGATAAGGGAAGTCAGGATGGTTTCCTGGAGGAGGGAGTGTTTGCACTGGTCCTGAGTGATGCGTAGGAGTTTTCCAGGGAGTGAAGAAGTCATTTCAGGAGGTGCTGGGACACAGGGTGGCTGTGTGGTCCACACAGGGTTCATGCTGGTGGGGAGAGGGGGACCGTGGCTTCAGGAAGGGGAATAACGTGGTTGGATGCCCTGGCCCAGCCAGTGCTGCCCCCAGGGAATGAGACACCTTTTCATGAGGTTCAGGAGAGTGGATCAGCTCCCTTGCTCAGAAATGCCTTTGTCCTCTGTCCCCAAGCTGCCACTTGGGGGAGAGGGGGGTCCCTGAACCAGGCCCCTGGGAGGGTGGCTCTGACCAACGTCTCTGCCCAG
Seq C2 exon
GGGGACTCAGGGGGGCCCCTGGCCTGCGAGAAGAACGGCGTGGCTTACCTCTACGGCATCATCAGCTGGGGTGACGGCTGCGGGCGGCTCCACAAGCCGGGGGTCTACACCCGCGTGGCCAACTATGTGGACTGGATCAACGACCGGATACGGCCTCCCAGGCGGCTTGTGGCTCCCTCCTGACCCTCCAGCGGGACACCCTGGTTCCCACCATTCCCTGCCTTGCTGACAATAAAGATATTTCCAAGAACCCGGCCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000109758:ENST00000382774:13
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.017
Domain overlap (PFAM):

C1:
PF0008921=Trypsin=FE(20.9=100)
A:
NA
C2:
PF0008921=Trypsin=PD(19.2=73.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGCAGCCCTGAGGTCTACG
R:
GGGCCGGGTTCTTGGAAATAT
Band lengths:
342-1302
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