Special

HsaINT0164006 @ hg19

Intron Retention

Gene
ENSG00000132405 | TBC1D14
Description
TBC1 domain family, member 14 [Source:HGNC Symbol;Acc:29246]
Coordinates
chr4:6995911-6998134:+
Coord C1 exon
chr4:6995911-6996029
Coord A exon
chr4:6996030-6998051
Coord C2 exon
chr4:6998052-6998134
Length
2022 bp
Sequences
Splice sites
5' ss Seq
AGCGTGAGT
5' ss Score
8.2
3' ss Seq
CTCATTTCTTTCCTGTCAAGAAA
3' ss Score
4.94
Exon sequences
Seq C1 exon
GAATATGAAGACAAGGCTGGAAGACCTAGCAAGCCACCCTCTCCAAAGCAGAATGTGAGGAAGAATCTTGACTTTGAACCACTTTCCACCACCGCACTCATCCTCGAGGACAGACCAGC
Seq A exon
GTGAGTTTAAGAAGACTCTCTTTAGAGTGTTTGCTTTAGGAAATAAGTACAACTTGCTAAGCAGCTTTTCATTAGAGAAAAACTAGGGTCAGAAAAGGGGAGAAGAGTAAGCCAGAATCACTTCTTATTCTCTATATTAACATGTGTTCTGTAATTATATTAAATGACCAATTTGGAAAACTGTCCTATAGCATAGAAGTTTTGACCAGGATTTTCCGTTCAGGTAATTTTTCTTTTTACTTTAGCATTTAAAAATAAGTTGTCAGCTGGGTGCAGTGGCTCACGCCTGTAATCCCTGCACTTTGGGAGGCCGAGGCGGTGGATCACTTGAGGTCCAGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAATACTAAAAATACAAAAAAATAGGTGTGGTGATGGGTGCCGTAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGCTTGCAGTGAGCCAAGATCACACCATTAATTACACTCCAGCCTGGGCAACAAGAGCAAAACTCCGTCTCAAAAAAAAAAAAAAAAAGAAGCAGTGTGTCTTCTACTATTTTCTTGTCCTTGAAAGTTGTATGCTGGGGAGAGAAATGGAGGACTGGAAAGTTAGAGGCCATCAGGAAAAGACTCTGGCCTTTGAAGTCCAGTCGTTTTCATGCTCTGAAAGGTGAACTGGCGGACTCTCCTGCAAGTGATGGTTGTTTAAAATGTCCCAGTGAATGTGGGTCCTGTTGTGTGAGGGACACAGGCAGCCAGACACTCCTGCTCTCCTTTTACCCTAGTGCCAGTACAGTTACAAGCACGCTTCTGAAAGAGAGCACGAATTGTATTTTTTTAAATGGGTTTTGAAGGTATACCAAGATGCTTAGAACTAAGGTGCACATCTGTGTATATGTCAAAAAACAAATGAACCACGTAGCTAGTATGAAATCTGTTCACTTTAAAAATCTGGTCAGGAAATGTCTTCATACATACATGTAACAAATGCTGTTAGGGTGCCCTGCCTCAAGAATTAGGTGTTGACAGTTATTAGTGTATTGCAGTCAAATCAAAGTTTCTTTGGAGTGTGGGGTGAAAATATACCAAAAGATTAAGTGTTTATCACTGTTGCAGTTATGGATAATTGTTATTTTCTTCCTGCTAATCTTTATCATTCATTTTTCCTTTCTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGCACAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCCTTCCAGGTTCAAGCGATTCTCCTCCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACGTGCCACCATGCCCGGCTACTTTTTGTATTTTTTAGTAGAGACAGGGTTTCAATGTGTTAGTCAGGATGGTCTTTATTTCCTGACCTCGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACTGCTCCCAGCCCATTCATTTGTTTTTATTTAATTAATTAATTTATTTATTTTTTGAGATGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAAGCTCCGCCTCCTGGGTTCACACCATTCTCCTGCCTCAGCCTCCTGATTAGCTGGGACTACAGGCGCCCGCCACCATGCCCGGCTAATTTTTTGTATTTTTTAGTAGAGACGGGTTTCACCATGTTAGCCAGGATGGTCTCGACCTCCTGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACATTCATTTGTTTTATAGTGAACTTGTTTTTGTTTTTGTAAGAAAGCATTATAAAAGTTTGTGAAAGAACTGTGTAATCTTAAAAAAATGAGTTTTTAGTGTTTGAGCTTTATATTTTTTAGGAAATTATGCTTCAGGTTTTTTCTGAAAGACTTCTATGCGGTATTTATAATGGTGAAAACTCATTTCTTTCCTGTCAAG
Seq C2 exon
AAATCTCCCAGCAAAACCAGCTGAAGAAGCTCAGAAGCACAGACAGCAGTATGAAGAAATGGTGGTTCAGGCCAAAAAGCGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000132405-TBC1D14:NM_020773:4
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.700 A=NA C2=0.834
Domain overlap (PFAM):

C1:
PF085986=Sds3=PU(28.4=62.5)
A:
NA
C2:
PF085986=Sds3=FE(31.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
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