HsaINT0076567 @ hg38
Intron Retention
Gene
ENSG00000143341 | HMCN1
Description
hemicentin 1 [Source:HGNC Symbol;Acc:HGNC:19194]
Coordinates
chr1:186172006-186174642:+
Coord C1 exon
chr1:186172006-186172131
Coord A exon
chr1:186172132-186174513
Coord C2 exon
chr1:186174514-186174642
Length
2382 bp
Sequences
Splice sites
5' ss Seq
TTGGTGAGT
5' ss Score
9.27
3' ss Seq
CATTGCCTCCATGTCTGTAGATA
3' ss Score
7.18
Exon sequences
Seq C1 exon
ATGTGAACGAGTGTAGACAAAATGTATGCAGACCAGATCAGCACTGTAAGAACACCCGTGGTGGCTATAAGTGCATTGATCTTTGTCCAAATGGAATGACCAAGGCAGAAAATGGAACCTGTATTG
Seq A exon
GTGAGTGTCTGGCTGTTTCCGTGACTGAGATCAGTTTGCCGTCAACAAGTCAAGTAAGGCATTCATTTTAAAAGAAGTGATTAGAGTAAATTTAAGCTAACAAGGAAATCTTTCTTTTTCCATAAGTACTCCCAACTTCTAGGATAATTGAGCTCCAGGTCCCAGGGTCATGGCTGTACCCGGAAATGGAAGCTCACTATGAAAACTTATGACCATTTTGAGCTCCCATCAATTAAACATTTGGTTTACATAGTTTAATATCCACAAGCATTAATATTATCTCACATGATTTCTAATAGAAATTTAGCATATATGTTAAGAATTTCTTGGGGGAAAGAAAAATTATGTCTGTAGAGATTAAAATTCAAAATATAATTATTTTGGAGATGTATATTCCTTAAATATCAAATCCATGACCAGACAAATAAAATAAATAATTTGCCCAAAATTTATGCTTTGCCTGTCTAGTCTACATCAATGACCAGACACAAAGGTACATTATAGTTCTCCCTACATTTGTTCTGTGTATGTCTAGGCTGTACCAGCCTGGTTAGCAGAGCTAGCAACTGCAGGATTTACAAAAATAAAAGAGAGATACCATTCCCATTCTCATTCCTGCTAAAAAACACAGGAGAAAGAAATAATTTATGGGTTAAATTGGCCTACTCCACTATACCCCCTCCCCCCAAAAAAGCAAAGACCTATAATATGAGGAGAATGAAACACCATAAAGAGGAACAAATAAAATTCTACAGGAATACCCAAGAGAGTGACTGTATCCAGTAGGAGTCACTATGAAGGAGGTCATGAAAATGATCACATTTAAATATAGGTTGGGATGTTACTAGATGGAGATGACAGAAAAAGGAAAGCAAGAAAGCCTTGTATAAGGGAGAAAGAGCTGAACTTAAGCATAAAGTGTTAAAATTCATTGTTCCTTCTTGACAGCTATCTAACCTTGGACAAGTCTTATGATTACACAGAAATTTGATTTTAAGTTTCTCATTGTAAAAATAGTACAGTTTTTCTTTTAAAAATCAATTATAAAATATTAATAAAATTATTGTATCTTGGATTTGTTTCAGAACAATATGATAGGAGTGGGAGATAGATATAGATGAAGGAATATTGGCCATTTGTTGATAGTTGTTAAGTTCATGGTGGTTTAGTATAATTTAAAAAAACAACAACTGGTGATGGGAGTTGAAGTATCAGATTTCAAAGACTTGTTTCAGCTCTTACACTATAGATATAGGTCAATACTTTCCTTATCATTTAAGAGTAGCAGCCAACTCGGTCAGGAGTTTTAGACCAGCCTGGCCAGCATGGTGGAACCTCATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCGCATGCCTATAGTCCCAGCTACTCTGGGGGCTGAGGTGGGAGGATCGTTTGAACCCAGCAGGCAGAGGTTGCAGTAAGCTAAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAGAAAAAAGAAAAAAAAAAAGTAGCAGCCAACTCAGAGCATCATGTACAGTTACATGCAACTGTAAATATTTTTCAGAATATTGGCCCTAATTATGTATAAGCTTAACTAGACATGAGTTGAAAGATCAGAAACTTTTTAAGAAGCTACAGCAAAAATCTAGCTAAGTGGGAATGGAAATGTGGAGATACATGGTTTTGATTGAAGGAAATAGAACTACCCAATCTTGGCAACTGAGAGAATAAGTTAAAGATGACTGACCATTGTACTTTGTATATAGCAAATGTTCAAACTAATACTATTACTAGAAACTCTTTTAAAAGAAATGCTTTTCCATAGCAGGAATACAGAACATAATTTATCATTTAAAGCTTGATGGACTTGAAACACAGGCCTGCTGTTATCACAAATAGGGGAGTAAGGTTAAGGCATTGAGGGTGTGCTGGGTTTGAACTAGTGGTAAAACAAAGAGAGATGGGGATGTCCAGCTAGCAGCTAGAAACATGGGACTGTAGATCAGAAGCAATGTAGCACTATTGCTCTCAATCTGCCTAAACTCTAATCACTTGTATAAATAAGATGGCAAAAGGAGGAAGGGATATAGAGAAGGAGAAAAAAAGAAATCTGTGAATAAAACTCTCTCCATAGTAGGGAGCAGGAGGAGGAAAAGCAGCCATTTAATAAGTGGCAGAGCTGGGACTTGAACCCAGGTTTTCTGATTCCAAGTTGTAAGCTGGTATGATCTCAACCACTTGGTGAGAAATGCAACCTTTGGCAATTCTACAGAATGCTGACTTTAAATACAATGACTTTGGGTTTGAAAGAGGAAATGTTACTTCTCATTGCCTCCATGTCTGTAG
Seq C2 exon
ATATTGATGAATGTAAAGATGGGACCCATCAGTGCAGATATAACCAGATATGTGAGAATACAAGAGGCAGCTATCGTTGTGTATGCCCAAGAGGTTATCGGTCTCAAGGAGTTGGAAGACCCTGCATGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000143341:ENST00000271588:102
Average complexity
IR
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:
PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.5),PF0764510=EGF_CA=PU(0.1=0.0)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Chicken
(galGal4)
No conservation detected
Fruitfly
(dm6)
No conservation detected
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