Special

HsaINT0075905 @ hg38

Intron Retention

Gene
Description
hepatocyte growth factor [Source:HGNC Symbol;Acc:HGNC:4893]
Coordinates
chr7:81757189-81758804:-
Coord C1 exon
chr7:81758692-81758804
Coord A exon
chr7:81757304-81758691
Coord C2 exon
chr7:81757189-81757303
Length
1388 bp
Sequences
Splice sites
5' ss Seq
AAGGTAACT
5' ss Score
9.01
3' ss Seq
TTATCTACTTTCTTCAATAGACT
3' ss Score
8.19
Exon sequences
Seq C1 exon
GGCTTTTGTTTTTGATAAAGCAAGAAAACAATGCCTCTGGTTCCCCTTCAATAGCATGTCAAGTGGAGTGAAAAAAGAATTTGGCCATGAATTTGACCTCTATGAAAACAAAG
Seq A exon
GTAACTGACTTCTCCCTAAATATTGCATAATGAAATAAAGTATAATGAAATGTATGTTTGTAATTTCCTGCCAGAGTGGTCTTTCTCACTGATTTTTCTACTATATATGAGATATTTTATGTAGTCAATTCATCCATTAAGACAGTTGAAACTAGTATCTTGACTATTTTTAGTATGGTACTTTAAGGAGAACATTTTCAAAACTTTTCATAATCTTGATTCCCTTCCTCCCTCTGTTTATTTTTATTTTTATTTTTTTGGAGCATCTCCTAGAACTGGCATTCTCCATGTTCATTTTAGAAAGTGCTACTTTCTTTCATTATAAAGTTTAAAACACTTTATATTACAGCAAATTCTGAGTTTGCTATAGTATTTTGCATTTAACAATGTTGGATAACTAAATTATAGTGATGATTACTGATGATAACAAAATATGGAGATTTTGGAGAAATGAGTTGGGACTATGTTTCATCATATACTTGAAAAAAATATTTAAAGGAGGAATTGAGACCATATTATTTGCTGATTGCCTATTCTGGTGGTCTGATATTATGTTCACTAGGTATTTACTTTGTTCAAAAGCAGAATCAAGTAAATGAAATAATTGAAGAATGTTAAACAACCATGTCCTATTAAATTCAGATACATAACCTGGTACAATATATAGATGTTTTCAAGTTAATAGGGTAAATGTTTAAATAAAATTAAAAATAAATTTATGGTAGAAGTAAGTTAATCTTTATACACCTCAATAATACTACAAATCTTGAACATAATTCATGATCTAGTATAACACCATTCTTACTTCAAACTGTCTTCTAGCTTGCTAACAACTGCATGTACTATTATTTGGTAGGAATATATAGGTTATTACAATTTGGTTGTCCTATCAGCAGTGGAAATGTTTGCAAAAATATGGAAACTAATAAGCAAGCTACCTCATGCATATGCATATATAAACAAAAATCCACACAATTTTACTAAGAAGGACAAATTAATTATCTTAGGTAACTTTTTGAATTCAATATAGGTTTTAAAAATCATTTAATTTTTGTTTTTAATATTTTCTTAAAATGGTCTATATATTTGAGCAAATCATAATTGCTTGGCTAGCTGAGTATACAGACTATGTTAAGTACAGCGACTGCTCTCTGGAGCTATCTATGCATATATACACAAAATTAAAACTTCTCAATCATCTGTTTGTTTTGGATTATTCAGAAATGTGTTATTTTGAAAATACTAGTAGAAGCTTTAGGCAAGAAATTTCAATGTTATTTGAAATAGTTTACAAGAGTTAATTACTTACAGGTTTGAACGGAATTTTTTTCTTAAATACTGCATATGTTTTGCATAGTTGCAATAATTTTATCTACTTTCTTCAATAG
Seq C2 exon
ACTACATTAGAAACTGCATCATTGGTAAAGGACGCAGCTACAAGGGAACAGTATCTATCACTAAGAGTGGCATCAAATGTCAGCCCTGGAGTTCCATGATACCACACGAACACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000019991:ENST00000222390:3
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=0.002
Domain overlap (PFAM):

C1:
PF0002421=PAN_1=FE(44.7=100)
A:
NA
C2:
PF0002421=PAN_1=PD(1.2=2.6),PF0005113=Kringle=PU(41.8=84.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGCTTTTGTTTTTGATAAAGCAAGA
R:
TCGTGTGGTATCATGGAACTCC
Band lengths:
222-1610
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