HsaINT0153402 @ hg38
Intron Retention
Gene
ENSG00000114923 | SLC4A3
Description
solute carrier family 4 member 3 [Source:HGNC Symbol;Acc:HGNC:11029]
Coordinates
chr2:219636302-219636874:+
Coord C1 exon
chr2:219636302-219636450
Coord A exon
chr2:219636451-219636679
Coord C2 exon
chr2:219636680-219636874
Length
229 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
CCGCTCCTACCCCCACCTAGTTC
3' ss Score
5.54
Exon sequences
Seq C1 exon
GAGAGAAGACCGAGGGGCTGATGGGCGTGTCCGAGCTGATCGTGTCCACCGCTGTGCTCGGCGTCCTCTTCTCTCTGCTGGGAGCTCAGCCGCTGCTTGTGGTTGGCTTCTCTGGGCCGCTGCTTGTGTTTGAGGAAGCCTTCTTCAAG
Seq A exon
GTGAGGCGAAGCCTTGCCCTGCTCCATCCATCCTGCCCCACACTCTTCCTTACCTACATCCTGCCCCACACTCTTCCTTACCTACATCCTGCCCCACACTCTTCCTTACCTAGGGGATGGGTCCCTGCATTCTCCCTCTTCCTCGGAGTTCATCCGCTGCCTATTCCAGGGGGCATTGACACCCAGGGCAGTCCACCTGTGGGTAACGACCGCTCCTACCCCCACCTAG
Seq C2 exon
TTCTGCCGAGCCCAGGACCTGGAGTACCTCACTGGCCGGGTGTGGGTTGGTCTCTGGCTGGTGGTCTTCGTCCTTGCCCTGGTGGCCGCCGAAGGCAGCTTCCTGGTCCGCTACATCTCGCCTTTCACCCAGGAGATCTTTGCCTTTCTCATCTCACTCATTTTCATCTACGAGACCTTCTACAAGCTCTACAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000114923:ENST00000273063:15
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:
PF0095516=HCO3_cotransp=FE(10.0=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=FE(13.1=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GAGAAGACCGAGGGGCTGAT
R:
AGGCAAAGATCTCCTGGGTGA
Band lengths:
292-521
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains