Special

HsaINT0153475 @ hg38

Intron Retention

Gene
ENSG00000033867 | SLC4A7
Description
solute carrier family 4 member 7 [Source:HGNC Symbol;Acc:HGNC:11033]
Coordinates
chr3:27418486-27420787:-
Coord C1 exon
chr3:27420700-27420787
Coord A exon
chr3:27418633-27420699
Coord C2 exon
chr3:27418486-27418632
Length
2067 bp
Sequences
Splice sites
5' ss Seq
GAGGTAATC
5' ss Score
7.05
3' ss Seq
TCAATATTTTTTTCACTTAGATT
3' ss Score
7.77
Exon sequences
Seq C1 exon
GTTTTTGTTTTTGTTATTGGGTCCAGCGGGCAAGGCACCACAGTACCATGAAATTGGACGATCAATAGCCACTCTCATGACAGATGAG
Seq A exon
GTAATCAGAATACTCCAAGTCTCTTTGAAGTAGACACTAATTATGCAGCATATAGTATATATTAGATTACAGTTCTCTTTTCTTTCATAGTGAAGCTCTAAAACTTTTCCTTGCTGTGTATACTGTTTTATCTCATATTTGCTTCTCCTATTTGCCTTCGGTTAGGTTTTTAAGACCTTTATATCAAGATCAGTGGGTATTTAAAAATTTTTTTTTGTTTTAAACATTTGTAATTATTGACTACCTTCTTGAACTTTCGAAATTTTGGGATTTTTTTTATCCTAGATTTCAGCATATCATTTCTCTAGGTTTTCCTCAGAACATTTTTTTTCCTGTAAATTTCTCTGATATGGGGTCCCGATCTTTGACGATAACCTACATACTAATCAGGACCTTGTCTTTCTTTTGAAGAGAGATTTGTAATCAGATTCTTGCCAAACATCAGTGCTGTGTGTCCCAAGGGTATTTGAAATGCCCCATATCTGAACCTGACCTAATTTTTCTTTTTCTTTTTCTTTTCTTTTCTTTTTTTTTTTGAGACAGAGTCTCACTCTGTTGCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCACCCCACCATGCCCAGCTAATTTTTCTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCAATCTCCTGACCTTGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGTCACATTTTTCTGTCCTCTTTCAACCAGCCAGTCACCAGATTCTTTTTACCTCTTCAATGTGTTTTGCATTTAATCTGTCATATTCTTTCCATCTCTACTGCCATTTCTCTGGCTTAGCCTTTTATTTGTTGATTCAAGTAGCCTTTATGAGTATTTATTGTATAGTATTTTTCTCTACACTCTCAGTAACATGCAAATTTGAATGTATCATTTCCTTAGTCCAAAGATATTAATGACTTCCTATCATATAGTGAAATTTAAATTTAAACTTTTGGCCGGGCGCAGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACTTGAGGTCGGGAGTTTGAGACCAGCCTGGCCTACGTGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCACAGTTCTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTACAGGCATACGCCACCACACCTGGCTAATTTTGTAGTTTTAGTAGAGATGGGGTGTCACCATGTTGGCAAGGCTGGTCTCAAACTCCTGACATCAGGCGATCCGCCTGCCTCGGCCTCCCAAAGTGCGGGAATTACAGGCATGAGCCACCGTGCCTGGTCAGTTACCTCCTTTAAGAGAATTTTCCTGGCTCCTTTGTTCTTTCCCATCAGTTTCCCTTTCTGTACCCTACTTTCTTTTTATCAGAGCGTCTATCAATACCTATAATTATTTATTTATTTAATAACGCGTTTCACTGTTTTTCCTCCTAGAAAAAAAGGTTCTTGAGTATAGGGACCTTGCCTTACCTGTCACCATTGCATTATCCACAATGCTTAGAATTGTATTTTAGCAGTTAGTAGGTAGCCAGTAAATATTGGTCATTAAATAAATTATTTAAGTAAAGTTGTTTGCATATCCATGATTATTTTCTTAGGATAAATGACATTTAAATGTCATAGAAGTAGAATGACACGCTACAGTGTTTTATTTTCTAATCAATTACTATTTCCCAGGCAAAATTTTATTTTTAAAAAATTGTTCTGTCTTAACATGTAACTGTTCTCTTTCATTGTTTGTTATTGTTAATTCATCTGATAATACTGAGTGGATTACCTTTTATAGTTGTTACCCAGGCTGGGCTGAATACCTGCCTGAGATAAGAGTTTAGGGGTTATCTTTATTGTGAAGCTATTTATGATATCCAGAGTGGATTTACTATGTGTAGAAATTTTTTTCAACTTTAAAATCTTTTACTCAATATTTTTTTCACTTAG
Seq C2 exon
ATTTTCCATGATGTAGCTTATAAAGCAAAAGACAGAAATGACCTCTTATCTGGAATTGATGAATTTTTAGATCAAGTAACTGTCCTACCTCCAGGAGAGTGGGATCCTTCTATACGCATAGAACCACCAAAAAGTGTCCCTTCTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000033867:ENST00000295736:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.004 A=NA C2=0.163
Domain overlap (PFAM):

C1:
PF075658=Band_3_cyto=FE(36.2=100)
A:
NA
C2:
PF075658=Band_3_cyto=PD(45.0=73.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
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