Special

HsaINT0153387 @ hg38

Intron Retention

Gene
ENSG00000164889 | SLC4A2
Description
solute carrier family 4 member 2 [Source:HGNC Symbol;Acc:HGNC:11028]
Coordinates
chr7:151075606-151076186:+
Coord C1 exon
chr7:151075606-151075775
Coord A exon
chr7:151075776-151076012
Coord C2 exon
chr7:151076013-151076186
Length
237 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGC
5' ss Score
9.6
3' ss Seq
CACCTGTCTCCGCCCCCCAGGTC
3' ss Score
10.84
Exon sequences
Seq C1 exon
GCCTCTCCATAGTTATCGGGGATCTGCTCCGGCAGATCCCCCTGGCCGTGCTCTTTGGAATTTTCCTGTACATGGGAGTCACCTCCCTTAACGGGATCCAGTTCTATGAGCGGCTGCATCTGCTGCTCATGCCGCCCAAACACCACCCAGATGTCACTTACGTCAAGAAG
Seq A exon
GTGAGCCCCCCAGCTCCCCACCGGAAGGGGTGTGCCTCTGGCCATCCTGGTCTACTTGGGTCACTCTCCAGCTGCCCCCTCCCATCTGCCCAGTTCAGCCAGCCCCCACCTCCTCTCTGTACCAACCCAGCTCTGGCACCTAGGAATGTTCTTCCATCCCCGCCTCCGAAGAAGAGAGAGGCTCTTCCCAGCAGCAGGCTAGGGAGGAAGCTGGGCTCACCTGTCTCCGCCCCCCAG
Seq C2 exon
GTCCGGACCCTCCGTATGCACCTGTTCACGGCCCTGCAGCTGCTCTGCCTGGCCCTGCTCTGGGCCGTCATGTCCACAGCTGCCTCCCTGGCCTTCCCCTTCATCCTCATCCTCACAGTGCCGCTCCGCATGGTGGTGCTCACCCGTATCTTCACCGACCGAGAGATGAAATGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164889:ENST00000413384:21
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0095516=HCO3_cotransp=FE(11.3=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=PD(2.2=19.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


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:
TGGCCGTGCTCTTTGGAATTT
R:
TCTCGGTCGGTGAAGATACGG
Band lengths:
292-529
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains