Special

HsaINT0086684 @ hg19

Intron Retention

Gene
ENSG00000116299 | KIAA1324
Description
KIAA1324 [Source:HGNC Symbol;Acc:29618]
Coordinates
chr1:109737043-109740276:+
Coord C1 exon
chr1:109737043-109737216
Coord A exon
chr1:109737217-109740095
Coord C2 exon
chr1:109740096-109740276
Length
2879 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGG
5' ss Score
11.08
3' ss Seq
CCTCCCCACTCCCCAACCAGGGT
3' ss Score
9.18
Exon sequences
Seq C1 exon
ATCCACTCTCTGTGCTACAACGATTGCACCTTCTCACGCAACACTCCGACCAGGACTTTCAACTACAACTTCTCCGCTTTGGCAAACACTGTCACTCTTGCTGGAGGGCCAAGCTTCACTTCCAAAGGGCTGAAATACTTCCATCACTTTACCCTCAGTCTCTGTGGAAACCAG
Seq A exon
GTAAGGTATACCAGTTGACAGGGTGAAAATTGAATGGGGGAGGCCCATGGATCAGAAGCCAGAGACAGACACAGGAGAAAACCAGAAATCCTTCAGGTAGCAGGGGGTTGAGGAGCTTCAAAGGTTTTTACATATTATTCTCCCTGAGGACTTTTTCCCCTAAAATTAAATAATCAGGATTATAAACACTTAAGAAAATAAAGATATTTAAAATAATGTGTTCTTGCCGGGTGCCTGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGACGGGCGGATCACCTGAGGTGGGGAGTTCGAGACCAGCCTGACCAATATGGAGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCTGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGAATCGCTTGAACCTGAGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCATTGCACTCCAGCCTGGGCAAAAAGGTGAAACTTCATCTCAGAAAAATAATAAAAAATCAATAAAATAAAATAAAATAAGGTGTTCTTTTACCTGACCTTTATTTCCTCAAAATGAGTCTATTTAAAAATATGCAGGAGGAAGGCTAGGCGCGGTGGCTCACGCCTGTAAACCCAGCACTTTGGGAGGCCTAGGTGGGTGGATCATGAGGTCAGGAGATCGAGACCATTCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCGTGGTGGCGGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGACAATGGCATAAACCTGGCAGGCGGAGCTTGCAGTGAGCGGAGATCACGCCACTACACTCCAGCCTGGGCGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAAAAACAAAAAAGCAAAAAACAAAACAAACAAAAAAAACCCCAGAAATATGCAGAAGGAAAGGTTTTTTTCCCTTGCTTGAAAAAGCAGTCTTCAGCAATCACTGCATTTGTCGCTTGTTTTCTAGAGGCTGGATAAAATCAACTGTTTCTAGTTCATCCACACGTCTCTTTGCTGACAGTATGAAAGAAAGTAACATGAAATGCTTTATAAGGAAAGATTGTCACCATCAGCCATTTCATGCTGCTGCAAATATTTCAGATCCAAAATTCAAAGGCAGAAATGCAAAGGTTAATCCCACCACTGCACTTGATTAAATTGCAACAAGCCACAATTAGCAGTTGGAAAGTTCATTTCAAATGTTACAAAAGAGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCAATTTGGAGGCCAAGGCAGGCAGATCACCTGAGGTCTGGAGTTCGAGACCAGCCTGGTCAACATGGTGAAACCCTGTTTCTACTAAAAATACAAAAATTAGCCCGGCATGGTGGCACACATCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTACTTGAACCCAGGGGGCGGAGATTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTGGACAACACAGCAAGACTCCATCTAAAAAAAAAAGTGACAATATAAAGAGCATCTTGAGCATCTAGTCTTTGACTCTGTTGGTGGTAAGGCCTTTACATCATAGAGCTCTGACCCATCTTCTGCAGCATGCAAAGAAGTCGATGGGTGTTTATAAAGAGAACATGTCAAGAAATAAACTAATCTATGAAAGATTAGAGATAGGTGTCTCTATCTTGTTTTCAGAAGTCTTCGAAGAAGTTAAAATGAAGCCTCAGAAGTAACAGGTCATGATCACTTAGGAAATAAGACTGATTAAAGCAGGCTTCATGTAGCAAAAGTGTCATTCAGTGAATTATGGAGAGCAATGAAGGTGGGGAATTTGGGGAAATGGTGTATTTTTTTATCTACTCCTTTCCTGTTTAGAAATGCTTATGATGTACTGCCACACGATAGATCCTTAGTTCAAAGACAAAAGAACTCTATTTTATTGTAATGTAAAGGTTTTCTTCAGTTTTCAAGCTCATCTACTTCCTACAATCTAGAAAAAAAAAAAAAGGCTGAGACACCAGATTTAGCACTTTTTTTTTTTTTGAGGTGGAGTCTCACTCTTTTGCCAGGCTAGAGTGCAGTGGCACGATCTCTGCTCACTGCAACCTCCGCCTCCCAGGTTGAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCATGCGCCAGCACGTCCAGCTAATTTTTGTGTTTTTAGTAAAGACGGGGTTTCACCACGTTGGCCAGGATGGTCTCAATCTCTTGACCTCATGATCCACCTGCCTCGGCCTTCCGAAGTGCTGGGATTACAGGTGTGAGTCACTGCACCCAGCCAGCACCATTTATAATAAAATTTATAACATTGAAAATGTTGACTGGGCACAGTGGCTCACCCCTGTAATCCCAACACTCTGGGAGACTGAGGCAGGAAGATTGCTTGAGCCCAGGAGTTCAAGACCAGCCTGAACAACACAGAGAGGCCCTATCTTTACGAAAAAAAAAAAAAAAAATTAACCTGCGGTTCCAGCTACTTAGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTCAAGGCTTTAGTGAGCTATGATTGCACCATTGCACTCCAGCCCGGGCAATAGATCAAGACTCTGTCTCAAAAAGACAAAACAAAACAAAAAAATCAAATCTGTCTCGTCATTAGACCTGGGATGAATCATTCCCCTACAACATACCATTGAAACGCTGAAAATTTAGATGTAAAAAAGCCTTCCCTATTCCCTTCTGGGAATTCCTCTGTGACCACTCACTTCTTCCTACTTCTTCCTCCCCACTCCCCAACCAG
Seq C2 exon
GGTAGGAAAATGTCTGTGTGCACCGACAATGTCACTGACCTCCGGATTCCTGAGGGTGAGTCAGGGTTCTCCAAATCTATCACAGCCTACGTCTGCCAGGCAGTCATCATCCCCCCAGAGGTGACAGGCTACAAGGCCGGGGTTTCCTCACAGCCTGTCAGCCTTGCTGATCGACTTATTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000116299-KIAA1324:NM_020775:15
Average complexity
IR-C
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:
PF076998=GCC2_GCC3=PD(15.7=13.8)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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