Special

HsaINT0153457 @ hg38

Intron Retention

Gene
ENSG00000188687 | SLC4A5
Description
solute carrier family 4 member 5 [Source:HGNC Symbol;Acc:HGNC:18168]
Coordinates
chr2:74224840-74227130:-
Coord C1 exon
chr2:74226957-74227130
Coord A exon
chr2:74224996-74226956
Coord C2 exon
chr2:74224840-74224995
Length
1961 bp
Sequences
Splice sites
5' ss Seq
ATGGTAAAG
5' ss Score
5.39
3' ss Seq
TTAGTCTCTCTCCACCACAGATC
3' ss Score
9.48
Exon sequences
Seq C1 exon
TTCTGGGAACGCTGCAAGCTCTTCCTGATGCCAGCCAAGCACCAGCCGGACCATGCCTTCCTGCGGCACGTGCCGCTGCGCCGGATCCACCTCTTCACCCTGGTGCAGATCCTCTGCCTGGCGGTGCTCTGGATCCTCAAATCCACGGTGGCTGCCATCATCTTCCCGGTCATG
Seq A exon
GTAAAGTGGGCACGGGCTTCCCCCTCCTGCCTGGCAGGTTGGCCTGGGCAACCCAGAGGTGCAGCGCAACCTCCCCTCCTGCCACCTTCTGCCTTCCTGTCAGCTGTGGCCTGGCTCCCTCGGGTCACGGAGGCTGGCACAGAATGACCTGATTTGAGTTGTGAGTCCAGGCCAGATGGTGTGGGGTGGGGCAGAGAGGAGGCGGAGGAAGGAATGTCAGAGCCGCTCAGTGAGAACCCAGGAGCCACCCTACCTCCTGGCTCCAGGGAGGGACGGAGAAAGAAAATCAGTTCAACCAGGAGACCGAGTTCCCACTGCCAAAATTCCAACCAGTCTCAGAAGTCGATGCGTACTAAATATAGATCTTTCCACCATTCAAGATAGCTAAATTTAAAAAGCTAAATAGTGAAGTAGGGGGGCAGGGGAAGAACGAGGGTCAGAGATCAAGAACAACAAAACCCAATGATGGTATATATAAAGCTTGAGCAAGGGAAAGGTTACAGGTCTTTCACTATTCTTGCAAATATTGTATAAGTTTGAAATTACTCCAAAATAAGAAGTGAAAAGAATGCAAAGCCAACAACATGTTGCATCTGGCCCCCTAGATAACTCACCGAGGGCAGTGACCCAGGCCCTTGCCAGGAGCCTGGAGTGTGTCAGCAAATGCCTGGGGAAAGCCTGAGGGCTCTGGGGTAGGGGACAAAGTAAGGACACTGAGGAGAACTTGAAGTGCACACTGCTGGGAGGGGTCTAGTCCATGGTTCTTGACCCGGGCTGCCCATGAAAATCAACCCAGATCAACAAATCAGAATCTCTAGGGAAACCCAGACTTTGGTATTTTTATGAGGTCCACAGGTGAGCATAGACCTGCAGCCAGGGTTGAGAACCCCCACTGCAGGGAAAGGGAGATAGATCCTCCCCCCAGTGCCCTCAGGGGCCTCAGAGCTGGCGAAGGGAAAGGCAGTAGTAGTCATGATTAGCATTTACTGAGTACTGTTCCACTGAGTCCACACCAGCCCCCAAAGCACTAATAACCCCGCTTTACAGATGAGAAAATGAGGCTCAGAGAGCATGAGCAGAGTGACCCTGGACACACAGCCAGATAGGGCAGGGCAAGACCCACACCCTCCACCTATTGATTTTTTTGTTTAATTTGCATACAGTAAAATTCAATGTGTGGGTCTATGAGTTTTGGCAAATGTACAGAGTGGTTAGAGACATAAATTCTCAGGCATTACCTGACCTGCTAAATCAGAAACTGGGGGAATCCAGTGATTTGTGTATTAATTAACAAGCCCTCCAGGTCCTGGTGCATGCTCAAGTTTGAGAGCCACTAATTTATGTATTTATTTTATTTGTTTGAGATGGAGTCTTGCTCTGTCGCCCAGGATGGAATGCAGTGGCACAATCTTGGCTCACTGCAACCTCCGCCTCCCGGTTTCTAGCGATTCTTCTGCCTCAGTCTCCTGAGCAGCTGGGACTACAGGCACCCACCACCATGCCTGGCTAACTTTTGTACTTTTAGTAGGGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGACCTCAGGCGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCCTGGCTGAGAACCACTAATTTAAAGAATAACTGTAGTTCTCCAGCCCATGGCCTTTCTGAGGCTCCCCACTTCGGCTGTCACAGGCTCCGTCCCTCTTGGTCACTGGTAGGCATGGTCACTCACCTGAGGGGCCAGACAAGAGGAACTACGGTGGAGGGAAAGTGAATAATGGCTTATGGGAGCTTCGAGACGGCTCCAAAGACACCACAAAAAGTCCCTGAACTCAGCCGACTGAGGGAGAAAAAAATCTATGCCTGAGTTTGGGCATTGAGACCACAGTTTTCTCCAAATTCTCACAAAACTTTAGTCTCTCTCCACCACAG
Seq C2 exon
ATCCTGGGCCTCATCATCGTTCGAAGGCTTCTGGATTTCATCTTTTCCCAGCACGACCTGGCCTGGATTGACAACATCCTCCCAGAGAAGGAAAAAAAGGAGACAGACAAGAAGAGGAAGAGAAAAAAAGGGGCCCACGAGGACTGTGATGAGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000188687:ENST00000377634:28
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.114 A=NA C2=0.395
Domain overlap (PFAM):

C1:
PF0095516=HCO3_cotransp=PD(58.6=58.6)
A:
NA
C2:
PF0095516=HCO3_cotransp=PD(1.9=17.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTCTGGGAACGCTGCAAGC
R:
TCCTCATCACAGTCCTCGTGG
Band lengths:
329-2290
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains