HsaINT0174079 @ hg19
Intron Retention
Gene
ENSG00000167094 | TTC16
Description
tetratricopeptide repeat domain 16 [Source:HGNC Symbol;Acc:26536]
Coordinates
chr9:130479908-130482457:+
Coord C1 exon
chr9:130479908-130480051
Coord A exon
chr9:130480052-130482356
Coord C2 exon
chr9:130482357-130482457
Length
2305 bp
Sequences
Splice sites
5' ss Seq
CAGGTGCCT
5' ss Score
5.4
3' ss Seq
ACTGTCCCCTGTGTCCCCAGGGA
3' ss Score
12.15
Exon sequences
Seq C1 exon
GTGGACTTCTATGCCTTACGGGCTGAGGCCTACCTCCAGCTCTGTGACTTCTCCTCGGCCGCCCAGAACCTGCGAAGGGCCTACTCATTACAGCAGGACAACTGCAAGCACCTGGAGCGCCTCACCTTTGTGCTCTACCTACAG
Seq A exon
GTGCCTGGGGCCTCCCGGGCCCATGCAGGGCACCCACCTCACACTTCTCAGGGGCTCTCCTGGCTCCTGGGCCCAGCTCTGTCTCCTTAGATTCCTCCTTGTCCCTGTGTCTGGGTCCCCCCCGCTGCCCCTCTCACCTCCAAGGCTGGTTTACTGCCAGGGTTGAGTCAAGTTTGGCAGCATTTTCCATTTGGGCTTTCTGCCATAATGACAGTGTCCAATATGCTAGCCACCAGCCACGTGGAACTGTTGAGCCCTTGAAATGTGGCAAGTGTGACTAAAGAACTGAATTTTATATCTTATTTTTATTTTATTTTATTATTATTATTATTTTTGAGACAGTCTTGCTCTGTCACCCAGGCTGCAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGTCTCTTGGATTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACACGCCACCACGCCTGGCTAATTTTTTGTATTTTAGTAGAGACAGGGTTTTACTTTGTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAGGCAATCCACCCACCTCGGCCTCCCAACGTGCTAGGATTACAGATGTGAGCCACTGCGCCCGGCCTCTTATTTTTATTTTAATTAATTTAAATGTGTATAGCCACACAAAGCTAGTGGCTATTGTCTTGGACAGAACGGCACAGATCTAGAGTCCAGAGGCTCTAAGCACTAAAAAGGTCACAGTGACCCCTAAGTGTATTTCAAAGGAAAAACAATATTAAACTATAAAACACCAACGAAGTGTTGCTTTTTTCCATTTTGATAACCTTGATGTCTTTTTTTTTTTTCTGAGATGGAGTCTTGCTCTGTCACCGAGGCTGGAGCGCAATGGCGCAATCTCAGCTCACAACCTCCACCTCCCGGGTTCAAATGATTCTTGTGCCTCAGCCTCCCAAGTAGCTAGGATTACAGATGTGCATCAACATGCCTGGCTAATTTTTGTACTTTTAATAGAGATGGGTTTTTGCCATGTTGGCCAGGCCGGTCTCCAACTCCTGACCTCAAGTAATCCTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCTACTGCGCCTGGGCTTGATGTCTTTTCTTTATGTCAAAAAATATTCAGTTCTTGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGTTGGGCGGATCATGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAAAAACTAGCTAGGCATGGTGGCACGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAACCTCTTGAAACCAGAAAGCAGAGGTTGCAGTGAGCCAAGATCGTGCCACTGTACTCCAGCCTGGGTGACAGAACAAGATGCTGTCTCAAAAAAAAAAAAAAATTCTGTTCTTAAAAAGAAACATTTGGGGCCCTCAGACCATGTGTGAATCTGTCTGTTGGGGGCCCATGTCCTGCACTGCCACTTCCTGTGTACCCTTGTGCAAGTCACTTCACCTCTCTGAGCCTCAGTTCCTTTATCCATAAGAGAAGCATGCTAGTGCCAGTGAGAAAACAAGTTCAAGTTCTTAGCACAGGGCTCAGCACCCAGGGCCCAGGTCCAGGCTACAGCCTGTTTGTGTTAGTTCTGCTGATCTCTTCTGCCATCTGAGTGTTTTGTTTTGTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGGGCTGTGGCACGATCTCGGCTCACTGTAACCTCTGCCTCCCAGGTCCAAGCCATTCTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCACTAACACACCTAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGCCTCAAACTCCTGGCCTCAAGTGATCCACCTGCCTGGGCCTCCCAAAGTGCTGGAATGGGATAACAGGTGTGAGCAACCATGTCTGGCTCAGCTATCTGAGTTTTCTACATTTCTCTTTGTTCCTGAATCTCTGTATTCCTGTCTCTTGCCAAGCGTGCATCTCTTACTGTCTCTTGCTGTCTTTCCCCAGATCTGTATCTCTCTCCATCTCTGTCTGTGTCTCTGCCTCTTCAAGTCTCTGCCAGATCTAAAAGGCTCTGTCCTTGTCTTTGTATCTCTCCCTCCTGCCTCAGGGCTTTCTGCTGCCAACTGGGGGGTGCAGCTGGGCTGGGGTGGCAAGCAGAATTGACTGTCCCCTGTGTCCCCAG
Seq C2 exon
GGACAATGCCTTTTTGAGCAGTGTGCCTTCCTGGATGCCCTGAATGTCTTCTCACATGCTGCTGAGCTCCAGCCTGAGAAACCATGCTTCCGTTACCGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167094-TTC16:NM_144965:4
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:
PF134141=TPR_11=PD(46.3=64.6),PF134141=TPR_11=PU(13.1=16.7)
A:
NA
C2:
PF134141=TPR_11=FE(54.1=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Rat
(rn6)
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
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)