Special

HsaINT0076642 @ hg38

Intron Retention

Gene
Description
hemicentin 1 [Source:HGNC Symbol;Acc:HGNC:19194]
Coordinates
chr1:186115258-186117115:+
Coord C1 exon
chr1:186115258-186115414
Coord A exon
chr1:186115415-186116993
Coord C2 exon
chr1:186116994-186117115
Length
1579 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGG
5' ss Score
11.08
3' ss Seq
CTTTGAAATGTGTCTTCTAGGCT
3' ss Score
7.98
Exon sequences
Seq C1 exon
TTCCTCCATCTATTGCTCCGGGTCCTACCAACATGACTGTAATAGTAAATGTTCAAACTACTCTGGCTTGTGAGGCTACTGGGATACCAAAACCATCAATCAATTGGAGAAAAAATGGGCATCTTCTTAATGTGGATCAAAATCAGAACTCATACAG
Seq A exon
GTAAGGATAATTTAAAACTCCTACCAACTATTTACAAACAGTTTGTAATGAATCAACATTTTAATTCTATCAGTGGGGTCAGCAAATATATAGACTATAACAAATTAGCTAGCATATAGAGGGTTTTTTTCCTTAATATGGACTTAGTTTTTCAGCCTAAAATATTTTTCTGAATTATAGGTCATCTTTTCCATACATAAACCCTGTGGATGAATGTCAGTGATTATATATAGGATTAGATTTATATCCTGCCTTATTTGTTTAGTACCTTTTGGACTTTTATAAAGGCAAAGGATAAAAACATCATTTTATATAAAAGAAAAACTATTCTGTAAAAATAAATACGATCTTTAGTTGTAGAATAAAAGTCAAATTTTATACCTTAAAATACAATTTAGATATTGGCAGAATGTGTAGGGAGGAAAAACAGCATTTTCTCCATTTTTTTTTTTTGCTTTTTTCCAAGCTTTAATACCATAGCTCATAATATGGCAATATCTATTTTTCAAAGGCTAAACTTTAAATCACTAAGAATTTCTGATGTTATAGGTGAGCATCATTTTTTGTATCTCACCTGAGCTATCAGATTATTACTCTGTCAAACATTTGCCATAGCGCTAAAAATAAATGCTCTCTTATGTCCACTTTAACAAAAATCAATTCCAATACATCAGGAAATATAAAACTAGGAGTGCTGCAGTTGAAATTCTATCATGTCTCTTTTTCACCCTTTTAATCTTTTGGCATTGGGAGGTTCAGTGACTTGAAAGTATACACTGTATGGAAAATGTGCCATGCTTTTGAATTAAAAGGTGTGTCAAATATGTTTTATTAATGTTTTTTATTAAATCATTTCTATCATGCACAGTGTGAAATCAAATAGATATTCTAATTTAGATTTACTTTAAATCATGTATGTGTATTTACTAAACCTCCTAAAATGTGAAGTGTTCTAGATTTTAGTTTTGAATATATATACACACATACACACACTTGTTCAAAACTAAATATATATATATATACTTTTTTTGAAATAGATATTGCCATATTATCTACAAGGTAGCCACACATTTAAGGAGACATGCAAAGTACATAAAGGGGTGAGACACACAGACTTGTCATTAGCCATCTGTCAATGGAAATAAACAAATATCAACCTGCTAGGTTATTGTGAAATTTAAAGATAATTTATGCAAAGCATTTAAGATGGTGCCTGGAGTGTATCTGATGCCCAGTAAACAGTGGCTGTTATCAGTGTTCTCATTGTACTGTATTTCTCCTAGGAGAGCCAGGTTGATCATAATATAAGCATTTAGAGAATGTAAGATTCCCTCTTCAGACAATCCTTCCCACAATTACTTCCTGTAAATATTATATCAAGTTTGAGGCTCTAGAAAGCCACTGCCATACAAACATAAACTCTAATGCATAAAGTTGGCCTCAGGGACATGATGTTAATTTTAACATGAGGGAAGAGTACTGTTTTCATCAATTTACAACATGGTACCATGTTAAACTAGCTGGGAAAATTTATGAAAACCTACATATAGTATCTCATGCTTTGAAATGTGTCTTCTAG
Seq C2 exon
GCTCCTTTCTTCAGGTTCACTAGTAATTATTTCCCCTTCTGTGGATGACACTGCAACCTATGAATGTACTGTGACAAACGGTGCTGGAGATGATAAAAGAACTGTGGATCTCACTGTCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000143341:ENST00000271588:75
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.094 A=NA C2=0.357
Domain overlap (PFAM):

C1:
PF0767911=I-set=PU(55.6=94.3)
A:
NA
C2:
PF0767911=I-set=PD(43.3=92.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCCTCCATCTATTGCTCCGGG
R:
GTGAGATCCACAGTTCTTTTATCAT
Band lengths:
270-1849
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