HsaINT0153482 @ hg38
Intron Retention
Gene
ENSG00000033867 | SLC4A7
Description
solute carrier family 4 member 7 [Source:HGNC Symbol;Acc:HGNC:11033]
Coordinates
chr3:27397684-27398353:-
Coord C1 exon
chr3:27398192-27398353
Coord A exon
chr3:27397798-27398191
Coord C2 exon
chr3:27397684-27397797
Length
394 bp
Sequences
Splice sites
5' ss Seq
AAGGTAACT
5' ss Score
9.01
3' ss Seq
ACATAATCCCTTTAACATAGGTG
3' ss Score
5.25
Exon sequences
Seq C1 exon
GAATGTAAAAAACTTCGTGGTGTATTCTTGGGGTCAGCTTGTGGTCATCATGGACCTTATATTCCAGATGTGCTCTTTTGGTGTGTCATCTTGTTTTTCACAACATTTTTTCTGTCTTCATTCCTCAAGCAATTTAAGACCAAGCGTTACTTTCCTACCAAG
Seq A exon
GTAACTGTGATATAATTTTGGAATTCTGGTAATATTCATATTTTTGGTTTTTATTTCCTTGGTTTATTTCAAAACAGTAATATATTTTTTGAGGTTAATACTCCATGCCAACTGGTTAATAAAGAAATTATTCGTAGTGAAAAATGTATATTACGTGCCTGAGCTCACAGTAGGAAGATGATGGTACCATAAGAGTTGCTAGGTTAGTTGCGAAATGTGTTTCTTATATTTTTGGAAAGAATTAAATATAAATGTGTTTCACTGTTAACATTGTCACTAGTTAAAAGCTCCATTTGTACGTTGTAGTGACAATTTTATCAATAAAAGATGTGAATTATTTAGAAAGAACACATAGTATTTCTGTGTTTATATTAACATAATCCCTTTAACATAG
Seq C2 exon
GTGCGATCGACAATCAGTGATTTTGCTGTATTTCTCACAATAGTAATAATGGTTACAATTGACTACCTTGTAGGAGTTCCATCTCCTAAACTTCATGTTCCTGAAAAATTTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000033867:ENST00000295736:17
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(10.3=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=FE(7.2=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TCGTGGTGTATTCTTGGGGTC
R:
CTCAAATTTTTCAGGAACATGAAGTT
Band lengths:
262-656
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains