HsaINT0108871 @ hg19
Intron Retention
Gene
ENSG00000128833 | MYO5C
Description
myosin VC [Source:HGNC Symbol;Acc:7604]
Coordinates
chr15:52553059-52556493:-
Coord C1 exon
chr15:52556387-52556493
Coord A exon
chr15:52553325-52556386
Coord C2 exon
chr15:52553059-52553324
Length
3062 bp
Sequences
Splice sites
5' ss Seq
AGTGTGAGA
5' ss Score
1.71
3' ss Seq
GCTTGTGCTTGTTTTTGAAGGAG
3' ss Score
6.51
Exon sequences
Seq C1 exon
GTTTCAAGGAGGATTTTCAGATGGACGTTTTTAAAATCCTGGCAGCCATCCTACATCTGGGCAATGTGCAGATCACCGCGGTGGGCAACGAGAGGTCCTCAGTTAGT
Seq A exon
GTGAGATGCTCATTTGTTTTACTTTTCCTTTGTCTAAGGGTCATAGTGGAACTGGCTCGCAGCTGACCTGCCTTTGCTTTTTAGCACCAGATATAGTCGGCCTCCTGGGTAGACTGGTTTAACAGGAGGCAGGCGGCAAGGGTTTCCAGGGCTTGCCTTCAAAGAGTAAAGCCTCCTCCCCTTGCAACAGTAGAGGAGGGGAAATGGATCTCCTGTGTGCTTTTCTTTTATTCAAAAAGTATGTATGAAGCACCTACTAAGTGCCACGGACTGTCATAGCATCTGGGGAAACAGCAGTGAACAAAACAAAGCAAGAAGCCCTTCAGGGAGCTTATGATCAAGGGTAGGGAGGAGACACAACAAGCAAATATGGGCTCTGGCAGCTGACGGCTGGCACAGAGGAAAGTAAAGCAGAGGGGGCATGCAGAGGTGCTGTGTCTTTCATGTGGGGTGGTCAGAGAAAGACTTTCTGAGAAGGTGGTGGGTGGCAGCCTGCAGGGGATGAAGAAGCAGGTTGTGCCTGTGGATGGGGGAAGAACAGCAAGTGCAGAAACCCGCAGGCAGGAGATGTCATTTGAAAAACAGCACGAAGGTCCATGTATCCAGAGGGTGAGTGACAGGGAGGGTGTGGATGAGGCCAGAGAGGGGAGGGGGATTGCAGACCACATAGGACCTTAAGGGCACTGGGTAGTTTTCAGCAGAAGGACACCCACTACCTCCTTACACCTGCTTGAATCAGACATCAGTGGTGCTGGCTTCCTGGGAATGTATTGTAAGTTTTGTGAAAGATTTCTTTATTTAATGGACACAAGTTAATTTGATGTGTGTTTCTTCTATGACATATACTATGAGTAGTGATTCTTGGGGGAGGGGTATGTGTTTAATTAGTCTCATCAATGTCCATGTAAAGAAGAAAACAAACACAAGTAAAAAATGTTTCTATGAAACACAGAATCTGCACACCTGTAAAGCTTTGCATTAACAATAACATGTCTGTCCTAGTCAACTCAGACTGCCATATCAAAATGCCACAGGCTGAGTGGCTTAAACAATAGACATTTGTTTCCTCACCGTTCTAGAGGCTGGAAGTCTGAGAACAGAGTGTCAGCCTGGTCGGTTCTGGTGAGGACTTTCTGCCTGGCTCCTAGATAGCCACCTTCTCATTGTGTCCTCATGGTGGAGAGAGAGCAGACACTGTGATGCCTCTTACGAGAACACTAATCCCATCATGGCAGGCCTCACCTTCTCAACTTTAGCCAACCCTGATTACCTCCCAAAGGCCCCATCTCCAAATACGGTCACATTGGGGGTTAGGACTTCAACATATGAGTTTTGGAGGGACACAAATGTTCAGTCTGTAATAATGTCTGTTTTCATGTCCCTCAAATAACTGATGGGAATAGTTGATCATTTTGTGTAACCGGTGAGTTCTTGGCTGTCTGCTACCAACGGTTTGGGGAGAGAGCAGAGCTGAGTGGAGCATGAGCTCCTGGGCTTAGCGTTTTAGGCCTTTTGCCATGACCAGGAAGTAATTCTCCTTCCTCTCCTCCAGCTTTCACCTCAGCGTCCATCCCATCCTGCCTGCAGTGTCCAGACCTCCCAGAATGAGTCAATTCCCCAAGTGGGAAAGCAGGGAGAGAGGTGACGAGAGGCCTGGGGGAGAGTGTGGTGTGTCTGAAGTGGCAGATCCCCCTCTGTTGCCTTGCTCAGTTACCTCAGAGAAGCTGGGCTTCTGCCCTTTTTTCCCCAAACCCCCATAGATTAAAAATGTGATTTCTACCCAACAAATGCCATCACACTGAGCCCTCTCCCGTGAAGCTTCTTATTAAGGTAGCATTTTGGAGGAGGAATTAAAATTGATTGACTGAAAATCCTTTGGAAAGGCTTCTAAGAATATTTGTAGAAAATTCCCAGTCCTATAATTATTGGTCCTAGATTTGGGATCCATCTCCACCCATTTGTATCAGGAACTTGAAATGTTGGACACGTTAAATTTGGACAAAGCCATCTGACTTTTTGAAAAGCTGCCGCCCCTTTGCATTTTTTTCCCATAGCAGCACCTGCAGCTGAATTGTTTTTGACTCAGAAGGTTTCATTCTTTCTTAGAAGGAAGGAAACCAAATGCCACTGCCAGTCCCTTCCCTTATAAGGTCAGGCACGTCAAAGCCAGCTCTGTGTTACTGTGATATTGGTCAGCAGGGGGTGTGGGTAGAGCGCAGGGAGGGGCAGGACTGTTTCCATGGCTTCCTACACTGTGTCCTGAGGCTTTTTAGTGCAATCATGTAGATTTCCTGGTGGGCTGGAATGGTGCCGGCAGGGGAGCCTGCCTTGGGAGTTCTCCTGCCTGAGAGAGGAGCTGGGAGTCACATCCTTGCCTGAGGACAGGAGCCCTTTGTCCACACTGGCTGAAGGGAAATGGGAGCACCTCTTCCCTTTTTTCATCTGCTGACCAGCGGGGCAGCTCTCATGCCCTGGCTTGGGGGAGAAGCAAGATTTCACTTTGTGTATTCAGGAAAAGTCCCACCCCAGCCCTCGTGTCAGCTGAGGCACTAGCTCAGCCATGGGACTCCCACCAGCTTCTGCCTGGCAGCAACACCTGGGTACCTCCTGGACCAACCATCCAGGCAAACCCCTGGCCACACGAGGTGGGGCAGGGTGAGTGCACACTCTGACAAGTGGCCCAGGATGGTTCAAAGGGAAGAGAGAGGGCTGCATCCACATCCACAGGAACAGGGCAGGGTCTAGAGAGGGTGGCCTCTATGGCCTTAGTCACCGCTGACATTCTTTGGTTAAAATGAAAAATCAGCGTGGGACGCAGCCCTGGACTCCCTGGCATTGCTGCAGGGGTGGTCTGCCAAGGGCCAGGTGCAGGACCCGTGCTGCTGTAGCCCCCTTGCTCTACTCCCAGGTCTATCTCCACCTCCTGAGGCTGGGCGTCCTTGTGCCAGCTACTACTCAGCTCTTGCACAGGCCTGAGTGTGGGCACGGGGGCCTTGGCCGGGTGGGATTGTGTGTCTTTGGATGGCTGGGCCACCTGACGGGGCTTGTGCTTGTTTTTGAAG
Seq C2 exon
GAGGATGACAGTCACCTGAAGGTGTTCTGTGAGCTCCTGGGCCTGGAGAGTGGCAGAGTTGCTCAGTGGCTGTGCAATCGCAAAATCGTCACAAGCTCTGAGACGGTGGTAAAACCCATGACCAGGCCTCAGGCTGTCAACGCCAGGGATGCACTGGCCAAAAAGATCTATGCTCACCTGTTCGACTTCATTGTGGAGAGAATTAACCAAGCGTTGCAGTTTTCAGGCAAGCAGCACACTTTTATTGGTGTTTTGGACATTTATGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000128833-MYO5C:NM_018728:9
Average complexity
IR-S
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:
PF0006316=Myosin_head=FE(12.2=100),PF114633=R-HINP1I=FE(28.0=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(13.1=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)