Special

HsaINT0083191 @ hg19

Intron Retention

Gene
Description
inositol 1,4,5-trisphosphate receptor, type 1 [Source:HGNC Symbol;Acc:6180]
Coordinates
chr3:4712413-4715071:+
Coord C1 exon
chr3:4712413-4712610
Coord A exon
chr3:4712611-4714819
Coord C2 exon
chr3:4714820-4715071
Length
2209 bp
Sequences
Splice sites
5' ss Seq
CAGGTGCGT
5' ss Score
9.73
3' ss Seq
GCCCTTGTTCCTTCCTCTAGATA
3' ss Score
11.46
Exon sequences
Seq C1 exon
GTTGGTTCTTTCTCGTTTTGAATTTGAAGGTGTCTCTTCCACTGGAGAGAATGCTCTGGAGGCAGGAGAAGACGAGGAAGAGGTGTGGCTGTTTTGGAGGGACAGCAACAAAGAGATTCGCAGCAAGAGTGTGAGGGAATTGGCTCAGGATGCTAAAGAAGGGCAGAAGGAGGACCGAGACGTTCTCAGCTACTACAG
Seq A exon
GTGCGTGGGACACGTGTGGGGCTCAGATTGGGGTGCCCCAAAACAGTGGCACTTAGGAATTTGTTGCTCGTTTGTTGATTACTTCAAGGAATCACAAGGAGTCATCTTGTAAGATTGTCTAGAAAAAAGCCAGATGTGTGTTTTAGGAGTTTGGAGTGTAAGATTTCAGTTAGTTGACATCTGGATGTGGCTGGTTCCCAAAAAGGATGAGTGCTTGCCTCAGTCCCTGGTGATAGTTTATCCTTCAGCAGCATGGCCCATAGATATGGTGGTAGGTACGTAAGAGGCAGGCTGTGGGGTCACATCCCTACCTCTCCGCTTACCAGTTTTTTGACATTGGCCAAGTTTGATTTTATGCTCTAATTTCTTTATCTGCAAAATGAAGGTGATAGTGCCAATCTCACCAAATGTTTATAGACAGAGACAGAAGATGTGTGTGTTTGTATACACATATATCTACACATTCATCCATGTATCTTTCTATAACTACACAAATATATAATAAAAAGCATGTACTTACACTAATACTTCCAATTCCATTCCAACACCATAGGATTTATTCTAGCCTTCACCTTTTCCATTTCATGACTCCCTCCAGCTGCCACGATTCCCTGTATGTTTACCCATCTGCCCGTTTCCCTGTGTGTACCTGTCTCACCTCTGCCACCCACCTCCACGGTCCCCAGTGTCTCCTTGGCTCCAGCTGTAAGACCTGCCAGTCCTGCCACCTGAAGGGAAGGGAAGGGGAAGAAAGAAAGGAAGTGAACCAATTAATACTTTTAAAAGAAAAGGAAAGGGAAGATAAAGCAAGGCTTTTATTATTTTTTAATAAAATAAATAAAACTGCAGATAAAATGCCTTTTCTTGCCTCCTGTATTCTGTTCTTTCATTCATGTGTGATGTACGCATCCTATCCACATTCTCTGTGTGCTGCATTTGTATGCATCTGTAAATCATATGTAGTATTTTATCTCTACTTAAAATTTTATATAAATGGGACTGTACTCCAAATACCATTCTAAAACTTGCCTTATTTATTCAATACGGGTACTGAAGCCATATTGAATATATCTGCGTTAATAGAGATTAATCCATTTCTGTAATTTGGACTGTTGGATGATATTCTGTTTTATTGATTTATCACATTTTCATCGCTGTTTGATATTTGATCACATGCTGCAGTTCTTCATGTCAGGAAACATCTTCATTCAAATTTTTCTGAGTATATGTATGAATTTCCATTCCACACTGGGAGGTGGGCTTGGAGGATATTCATATTTTAAGCTTTACTAAGCAATTCTAAATTGGATGTGTCAGTGTACACACCCACCAGTTGTAGACGACAAGCTTTGTTTCTTCATGTCTTTGTTAACCTTGAATATCATGATGCTTTTTAATTTTTGGTAATTTTATAAGTGTGAAATAGACTCATGTCTACACTTGCATTTCCCCGACATCTAATGAGGCTGAGAATGTCTTCAAATCATGATTATTAGAAATACATAGAGTTTTTAATTCAGAAGGCAGTATTTTGAAAGCCTGTGGCTTTCTCGTTATTTCACATTTCAAGTATGTTTACTCTTTCAGTGTTTGATGAATCTTCTCCCAAGTGAATGAGAAAGAGTGCCTTAATTGGTCAGGTTCCAGTTAACAACATTCACTTGCAATTGGATGAAGATGAAAAGTGAGGAGTCTCCTACTTTTGTAAATGAAATGTTTTTTTACACGTGTAGGAATTAGAGTGACTTACATGATATAAGATCTTTAAAATGTTATAAAATTTCTAATTAGGCTGAATATGTGTGATATCTTGAACATTTCCTACATGGTCTTTACTGTATAAAACACAGCTGAAGGGAAAGAAATAGACAACCATCTTAGGCCTTAGCATTCCCCCCGTTTATTTTAAAAAGTAAACATTAAGGACCTAGTGGAATTAGGTCGTCACATAATTGCTCCAACACAGCTGGATAGACATGTGTTCCTGTTGGCTGTCAACCCACACTCTACTGCACAGCTTGAATAGTTCTTTTATCTGCTTGGTACCAAAGCCAAAATCCTGGTATACAAGAGCAATTTAGGGGTGTTGATGTATGAGTTTAGTTGGCCAAATGTCACTCCCATGACAGTCAGGGCTGCCCAGACGACCCTTCATTCATCCTGAATGATTTCTGGAGCGTGAGCTGTGTGCCCTTGTTCCTTCCTCTAG
Seq C2 exon
ATATCAGCTGAACCTCTTTGCGAGGATGTGTCTGGACCGCCAATACCTGGCCATCAACGAAATCTCAGGCCAGCTGGATGTCGATCTCATTCTCCGCTGCATGTCTGACGAGAACCTGCCCTATGACCTCAGGGCGTCCTTCTGCCGCCTCATGCTTCACATGCATGTGGACCGAGATCCCCAGGAACAAGTCACCCCCGTGAAATATGCCCGCCTCTGGTCGGAGATTCCCTCGGAGATCGCCATTGACGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000150995-ITPR1:NM_002222:19
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.060 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0136516=RYDR_ITPR=PD(3.9=11.9)
A:
NA
C2:
NO


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
  • Pre-implantation embryo development