Special

HsaINT0025519 @ hg38

Intron Retention

Gene
ENSG00000160325 | CACFD1
Description
calcium channel flower domain containing 1 [Source:HGNC Symbol;Acc:HGNC:1365]
Coordinates
chr9:133459987-133463555:+
Coord C1 exon
chr9:133459987-133460187
Coord A exon
chr9:133460188-133463482
Coord C2 exon
chr9:133463483-133463555
Length
3295 bp
Sequences
Splice sites
5' ss Seq
TCTGTGAGT
5' ss Score
7
3' ss Seq
CCCGTGTCTCTTGTTTCAAGCTT
3' ss Score
7.93
Exon sequences
Seq C1 exon
ACAAGGCAGCGCGCCGGCTCGGACGCGGCCGGCTACCGAGCCCTTTGTGAGGGCTGTGAGCTGCGCCTGACGGTGGCACCATGAGCAGCTCAGGTGGGGCGCCCGGGGCGTCCGCCAGCTCTGCGCCGCCCGCGCAGGAAGAGGGCATGACGTGGTGGTACCGCTGGCTGTGTCGCCTGTCTGGGGTGCTGGGGGCAGTCT
Seq A exon
GTGAGTATCCAGTCGGGGAGAGGGGCCGGCCCCGCCGCGCATGCGCTCCTCGCCCTGCCCTGCCCCGCCCCGCCCCGGCGGCCCCAGGGGAAAGGACCCGCTGGGGGTCGGGGGTCTGCCGGGCGCCTCCCGGGGCGGAGGAATGGCGGGGCCGCCGGGAGCCGGCGTCCTGGGGTTGCCATGGTTACCCGCTCGGGCCTGGGCGCCTTGGTACCCCGGGCTGGGCTGGGCTGGCGCTTCTGGGAACATTCCCGGAGGGACCAGAAACCCCAGGGCGGGGGGGCGGCGGGGGCGGGGGTGGGGCACCGGCCTGGGGCACGTGACTGAGCCCTCCCCCCGCTCCCCAGGGGCTTTTGTGAGACTTTCTCGGTGATGCTCACGGGGCGCATGCCCACCTGGCCCGTACTAAAGCGTCAACTGTTGACTTGGGCGTAGGTGACGGCAGCCACATTGCTAACCTTTGGGCAAGGATTGTTTGTAAGGGAGGCGGGTGCACGGCTGGCTAGATTTCTGGCAGGAAGCCACTGGGCGGAAGTTTGCTGAGGGTCAGGTGGTGTCAGGGCACAGGTGGCCCCTGGGGCCGCGGGGCAGTGAGCTGAGGGCCCGGCCTCTCCCTGGGTCCTCTGTCCGCTCTCATATCTCCCCCGTTGCTGCTGCCTTAGCCGCCTGTCACCGGCCTTCCTCCCCTTCTCCGCACGCATCCCAGTCACAGACCCTGACCTTAGGCTGCCAGGGAAGCTAGGCTCTTAAGCACAGCCAGAAAAGGACAAAGAGGGAGGCAGGTCAGCTCCAGGAGTGAATGGAAGCCGTACAGCTGGCCTTCCAGGGAAAGACAAGTCTGTCTGAGTGATACCCTTTCCTTTCCTGTCTGCCCTCAATCTTGTGGATTACTGGAGTGGGCAAGGTCTTAGAGAATGTCTGTCGAGGATGTCTGCAGGTTTTAAACAGTGCCTGCCTGGCAGAGAGGGCTAGCTCTGGGCCTGGGCAGGGCAGGCCCCATCAGCAATCCTGCCAGAAGGACCACCTTTTCAGGGTCACCTTGGGTTCCACAGCCTTTCCAGGTGGGTAGAGGGTGGAGGGAGGTTGAGGCAGGAGGGTGCTGGGCTAGGAGTGTGCTGCCCTCGCTAGGCATGCCCTTATCCAGAGGCAACGGATACGGTAGGGCAGGCCCTACCCCCAAATCACAAAAAGGCCCCGAGTTTGTGTCACTGCTCTTCAGGGCAAGTACGCTTTTGACTTTGTAGGAGAGACTGGTGGGTTTGAAGTTAGGCATTGGATCCAGTCCTGTCATGTCTGGTTAGCTGTTTTCCCTGCAGATTAGGGTGGGCAGTGCAGTGGGGTGACATGGTCAGTGGTGAGAAAGGAAAGGTCCTGACTATGGCCTGTAGGCCACACCTCCTTCCTTCTTGGTCAGTGGCCCTGCCGACTCCCAGATTTGCTGTGGAGTCTTACTCAGTTCTGTGCCTCTCAAAGTGAGGTACCTCTGCCTTTCCTGGGAGTTCCTGGGGCTCTGTTGGGTCTACAGATGAAGCTTCAGGAGAAACTTGTGGCATTGCCCTGAGTTGTCAGTTGCATCTGCAGATTTTTGGGGGCATGGTTATGTGAACATCAAAATGCTGTATTACAGGGTAGAATGCAAAAATGCAGGGTGTTTTAGAGATGCGGCAGGAGTTCAGACAAGGGTTGTGTGCCGGGCTGGTCCTTGGGTAAGGTTTTCCTCCTCCAGGGTGAGGGGATCAGAGAGAGTACCTGGAGAGGGTCTACCCTGGGTCCTAAGAGCATCTGGAGGTGATACCTTGGGAGGGGACAGGATTGCATGGTGACAGCCCCCTCACGTGGAAGATATCAGCATTGAGGCCCCCAAGTGGACATCCTCCAGCCCTTTATTGCTAAAGGATTCCTGGCTGGAGCCTGCTGGTCTGGCTTGACACCTGGTCCTCCCCCAAGGCTGGCTGTGGGTTGGACAGCTGGGGTAGGGTTGGAGCTGGAGGCCAAATGCTGACTGCAGCAGGAAGCACAGCCGAGCTGTCAGGTGAGGCCAGGCACAGCAGAGAGGCAGGGAGCCGTGTCACCCTTTGGGCACTCTGCTAGGACAGGCAGGCCCCTGTGTACCTGTGGTTCTGGAACACCTTGCTGTCTGAAGGCAGATGTCTAAGGCTGTGCTGAGGAGCAGTGCAACGCTTGAGTCCTTTGTTTTAGAAGGAGACCCTGGGGGCCCATGAAGCAGTCCCATTGCAGTTCGGCTCACTTTATCTGGCTTCTTTGCCTGCTGTCTGCATAAGGTTACCTGGGAAAATGGAAAACAGCAGAATTCCAGACCCAGGTGGAGGGATCAGGTGCAGAGGAGCTGCTGCAAGTTTAATGAGCTGGGTGCTAATTGCTGCCTCCAAGGCCCCCCTCAGTGATGGCCTGGGCTTGCTCCCTGCCCAGCAGCCACCTCCTTGGACCTGCCTTGAAGGCTCCTGGAGTTCCTGGTGAAGCCAGGCTGCAGGCTGTGGGTGGAGGAGGGAGTTGGGTGCAAGAGACCCTGCTGGTGAGGTGCAGCTGGGAGGCGGGGCGTCAAGGCTGCACATCTGAGCATCAGAGAAGCCACGTTCTGGGGTGGAAAACGATGCCCCCTCCCCTTCCTGGCCTTATGGCATTTCAGCGGTGGGTGGCTGGGCTGTGGGACTTGCTCATGTGCAAGAGGAGAAACGGGTCTAGGAAGATGAAGATAGCGTGCCAGTGGCACAGGGCTGGTGAGGAAGTTAGAGCTGGAACTGCTGCTCAGTCTTACCTGGTTCCCATCTCTGTTCTGAGAGAGGCACCCCTTGTCCCAACCAAAATCCAAGCCACATTTTCTGAGTCAGAGGACTTCTTGTGTGGCCGGCCCTGTGAATGGTGGCAAGTGACCCTTACCGAAGGCTGAGTCTTGGGGGAGCACTGGCCTGAATCCTTGAGGGACATTCACTCTTTAATCCTTCTTTAATCCTAACCTCCCTTTGAGGTGGATATTGATGTAGCTGGGGTCAGAGGGCCAGCTCCTCTGAGCCCTGAAACGGGGAGAGGATGCTGTGAGATCCACCTGCCACCTTGCTGCCACCTTGCTGTGGGGCCTGGGGCAAGCAAGGCACTGCACCTCTCTGCGTCTCCTCACCTGTCTCAGACGATAGAGGGCAGGCTTCTGGGTGCTGTGAGAACTGTGTGCTGAGCATCCGCAGAGACTCTCGTCCTTTCCAGTCATCTCCCAAGGCCGCCTTCCCAGCGGGCTCCGCCTGCCTCCCTGCTGACTCCTGCCCGTGTCTCTTGTTTCAAG
Seq C2 exon
CTTGCGCGATCTCTGGCCTCTTCAACTGCATCACCATCCACCCTCTGAACATTGCGGCCGGCGTGTGGATGAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000160325:ENST00000316948:1
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion (1st CDS intron)

No structure available
Features
Disorder rate (Iupred):
  C1=0.105 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF102334=Cg6151-P=PU(6.4=17.1)
A:
NA
C2:
PF102334=Cg6151-P=FE(70.6=100),PF102334=Cg6151-P=PU(7.5=12.0)


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:
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