Special

HsaINT0152515 @ hg38

Intron Retention

Gene
ENSG00000157765 | SLC34A2
Description
solute carrier family 34 member 2 [Source:HGNC Symbol;Acc:HGNC:11020]
Coordinates
chr4:25667880-25669842:+
Coord C1 exon
chr4:25667880-25667991
Coord A exon
chr4:25667992-25669646
Coord C2 exon
chr4:25669647-25669842
Length
1655 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGA
5' ss Score
10.57
3' ss Seq
TCGGGGTTTCCCTCCCATAGAGC
3' ss Score
8.26
Exon sequences
Seq C1 exon
TGCTCACTGTTCGGGCTGCCATCCCCATTATCATGGGGGCCAACATTGGAACGTCAATCACCAACACTATTGTTGCGCTCATGCAGGTGGGAGATCGGAGTGAGTTCAGAAG
Seq A exon
GTAAGAGGCTCAAAACCAGCCTTTGCGACATCAGCTCTATTGTTCTTGGCCACGCTGTTGTAACTGCTTTTAACCAGCCAAAGATGACATGCTTATCAGGTTCATTCCTGGAGTTCCTAGAAGTAACCACAGGGAGGTATGGCTAGGGTTGGATCACATACTCACCAGCTGATTAGACTCAGCTCCCTGATCGGCAGAGCAGGGATAATACTATCTATCACTACTGAGTTGTTGTAGGATTAAATATACAACCCAGCAGGTGAGTGTTCAGAGCACCCAGCACATTGAGTTCACTAAATAAATGCAAACTCTAGCTAGAAACTTAGCCGCTGGGTGGCGGAATTGAAGCAAGGCCAGTTAGAAGAGTAGGATTTATTGGGACTGGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTCTGGGAGGCCCAGGCGGGTGGATCGCCTGAGGTCAGGAGCCTGGCCAACATGGTGAAACCCCATCTCTTCTAAAAATACAAAAATTAGCCGGCCGTGGTTGCCAGCGTCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGTCGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCCATCTAAAAAAAAAAAAAAAAATAAATAAATACTGTTTTGTTTGGTCATAATTATAACTTATTTAAACTTCCACTTTCGGTCAGCTCAACCCATGCCACCTTTTCTTTGTTCTTCACTTACAAGTTAATAAAAAACAAAACCTAGTTTCTGCGTATGCAGAAACTCTGAAACTAGAGCAGGTAGAATGCTGGAAACTCTTTTCTTTCAAAAAGGTTAATGTGAAAATTAAGTGTTTCTTAGCCTCTTCTAGCTAGTTTTTTTTTTTTTTCAGTTTTTTTTTAAAAGGTAAGCTGTTTCATTGAAGACATAAAAATCCAGAACAGAGTTTTTTAAATCTGGAGATAAGATGGAATCGAGGAGGAATCTTTGAACCTCCTCAGATGGATGCAAAATGTTTTAGCCTTGTTTCCCATGGAAACTATTCATGTTTCATCACTTTCAAGAACTTAAAAAAAGTTTAAGAATTCACTTGCATAGAGGTCTTTTTAAGTTAAATTTTTTTATTGATACAAAATATTTTTACACCTTTCTGGGAAACATGTGATATTTTGTTACATTCATAGAATGTGTAGTGATCAAATCAGGGTATTTGAGGTGCCCACCGCTTTGGGGATTTATGATTTCTATGTGTTTGGAACAATTGAAAACTCCAGCATAGAGGGCTTTGGTTGCCTTCATACTGGTCCCCACCTTTCCAAAAGAAGGTAGCCTTCAATATACATGATACAAAAGTGCCCTTGATGCAATTCTTCGAAACAGTGATTGCTGAGCTAATTATTCCAGCCGTAACATGCTTGCTGGCCCGCAGCTTCTTCATCTGGCCAATGGGAATATAGATACCAGCCACTTTGGGGATCGATATGAGAGAACAAAAATGAGATTGTGTACATGTGCACACTTCCATAGGTGACACCTAGCAGAGGGTGGCAGATGATACAGGTAATGACCCACCTCACATGGTGCCCACTTGCTTAGTGACTAATCTGGCTGTCGGGGTTTCCCTCCCATAG
Seq C2 exon
AGCTTTTGCAGGAGCCACTGTCCATGACTTCTTCAACTGGCTGTCCGTGTTGGTGCTCTTGCCCGTGGAGGTGGCCACCCATTACCTCGAGATCATAACCCAGCTTATAGTGGAGAGCTTCCACTTCAAGAATGGAGAAGATGCCCCAGATCTTCTGAAAGTCATCACTAAGCCCTTCACAAAGCTCATTGTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000157765:ENST00000382051:6
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=0.000
Domain overlap (PFAM):

C1:
PF0269010=Na_Pi_cotrans=FE(25.7=100)
A:
NA
C2:
PF0269010=Na_Pi_cotrans=PD(28.5=62.1)


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:
CTCACTGTTCGGGCTGCCAT
R:
ACAATGAGCTTTGTGAAGGGCT
Band lengths:
302-1957
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains