Special

DreINT0013237 @ danRer10

Intron Retention

Gene
ENSDARG00000104868 | KCNT1 (2 of 2)
Description
potassium channel, sodium activated subfamily T, member 1 [Source:HGNC Symbol;Acc:HGNC:18865]
Coordinates
chr5:64830036-64833304:+
Coord C1 exon
chr5:64830036-64830119
Coord A exon
chr5:64830120-64833209
Coord C2 exon
chr5:64833210-64833304
Length
3090 bp
Sequences
Splice sites
5' ss Seq
ATTGTAAGT
5' ss Score
8.54
3' ss Seq
TATTCTCTGTGTCTTTCTAGAAT
3' ss Score
10.72
Exon sequences
Seq C1 exon
ATCTTTTGGCCTCCGCTTAGGAACATATTTGTTCCTGTATTTCTTAACTGTTGGCTTGCCAAATCAGCGCTGGAGAATATGATT
Seq A exon
GTAAGTAATATTTGCAACTGTGCAGTGCGTTTCACATGCCTGTGGGAAATCATGCTGAATGACTCTGTTGTTATTTGATGATATGCCATGTTGGGATGCTTTACTTCGGTATGCATTTGACAAACGAAAATGCATCATCAGTGAAAACTGAGAGGATGCCAGCACTCCAGTCCCTGCCAGATGGTTGGGTCAAATGTGCAGAAAGAAGCTGGCAGGGGGGAATGTCCTTTTACAAATGCTTAAAGCAAAGATATTAGTAGAAGAGACATGCTAACAATCTACAAAATGTGACATGCATTCTTAAAACACAATCTCTTTATTAGCATCAGTTGTTTAATAAAGAATCTTCCATGGAACGTTTATAGTGGAAAAAGGTTCTTTAGGTCAGTGGTCCCCAATCAGCTCTTCTAGCTCCAAAAGGATTACAATTTGTATAAGCCTTATATACTAGTCAATACACTATTATTGTGGCATTAAGAAATTAATGGCAGAAAGATTAAATGCATGAATGGCTAGACAACATACTCAAAAAGGATGGTATAGTTAAGTGAGGGTAGGTGACGCAGTGGTGCAGTAGGTAGTGCTGTCTCACAGCAAGAAGGTCGCTGGTTCGATCCTCGGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTTTCCCTGCGTTCGCGTGGGATTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGATTTGGGTAGGCTGTGTGTGTGAATGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGTGTAAAAATGTGCTGGATAAGTTGGCGGTTGATTCCGCTGTGGCGACCCCGGGTTAATAAAGGGACTAAACCGACAAGAAAATGAATGAATGAATAAAAGTGAGGGTGGCATATGTAATTTATTAAACAAACAAATTCTCTTATTATTTATTTTTTCTTTTATTATCCTTATCTTATATTTCCTTCCTTTGTTGTCTGTAAAGTGTGTTGGTCTTTTTTCACACTTTGTCTTTCTATGGTGACTTGTGAGTTTGGCGATCTACTGAAAATGCCGTCAGGTATGCGCCGTGCGCGCACATTAACCTGTGGTTATCTTCAGGAGGTTGATTTAACTAACACTTATCAGCTGTTTTGGAACCGACATACTGTAAGCAGGTATTAGCTTTTACCAAAACTAATATAGCAATTTTTTTTTTATTTGTGTATGTGTGAAAAAAATATATAATTTGCACAAAGAAATGATGGGATTCTTCTTTAAAGAAGTTGTTACCAACTCGTTTAGAGCATCATTATGGGCGTTTTACGTTATAACTAACAGGGTTCAAACAATGGATCTGCAAGAGAGAAACTACGGGTTTTAAGAAACACTCGTCACCACATCGTTCTTTTCTCAAATGTTGCATTGTACTATGATAGTTCATCCACAAGTTACGTTGTTGTTTGGGAAACACACCCCTTGGGCTCTATTTTGACGGTCCATGCGCACTTTCATTTTCACTACATACTTTCACTTTCGCTCTTGTATAGGAAAACCTTTACGCACAGACATCAATTAGTCTATAAATAATTAATTGCGTTTGTTAAGCGCAAATATTCGTTTCAAAACTATTTCTAAATTCAGTTCTAATTTCCAGCAAACTAATAAATGAACAATATTACCGAAGTGTTATCCTGAGTTATATCCTAAAACACATGCTGTGCCCCATATGGTCTAAAACCTGACAGGTGGGCAAATCTAAGCTTGTTTTTATTAAAACAAATATAAATATGGATATAATAAATAATACTGCTAATAATAATAACATTATACAAAAGCAAATTGTTATGAATGAACTGAAAAATCCTCCCGAGATGAAGAAGACATAAGAGCAGTGATTTTTCATATTTATGTAGGCTAGAAAATAATATGTTTTGTAATATTTTAATCCTTTATATTTATATTCTATATATATCCTTAATATTTAATTTTTTTCATATGTAAAGATATTTGCCTATTGCTCTCTTGTGCGTATTAAGCAGTGCGTAAGCGAGGCGCTGGAGTTTAGACCGGGTTTGTTTTGGTCTAATGAAAAATCTATTATAGTTTCTCAAAATAGCAACGCGCCAGCAATGCGCCTCAGAACGCCTTCCTTTTTAGACCAAAACGTCTATGGGCGCACATATGAGCGTTAATGCATTTGCTATTTAAACATATAGCGCAACGCCTCAAAACCACTCTTGCGCCAAGCTGAAACTACCAAACAAGTATCACGCCACATTGCGCCGGGTGTATGATAGGGCTTCTTATCTCTAAAGCAACTATTGAATTCACAAGTGTATCAATCTTTGTCCAAATGTAGAGTTCTACTATCTCCCAAATAAAACAAACAAAAATATTATGGAAGTCAATAGTTACCAGTTTCGAACATTCTTCAAAATATCTTCTTTTATGTTCAACAGAAGACAAAAGCGCAAACAAGGTTTGAAACAGGTTTGAGTCTTCTGAAGAGAAAATGATGGCTGAATTTTCATTTATGAGTGATCCCTTTAATTGTGAGAATTGGTCTCTAAACTGATGTGTTAACAAAAACTGTTTAGCTGTTATGTAACTCCTCATTGAACGATTATTTAATGATCTCTCTGAAAAAACAAAACAATTTTTGGAAGCTTTTTCCATATCTTAAGTCTTTTTTTCTTATAAAGTTTTCCTTGGAAACTTTCTTAAAAGATAGTATCCTAGAGAGATGACTATTACAAAACTGAGTAAGGAAGCTATTTCAGGCCTGAACCCTTTGTCAAAGCACTGTAGTGAACATGCATATACAATAGGCCTACAGTATATGTCATATATCTGAGAAATACACTTCTTAAGCAGTTTTACTTGTATATTTTACTCTATATAGTTCAGTTGAATTGAAAAACTAGTTATATAAGTCACCCTAGACTTCACTGTGCAATAAAATAAAGATAATGATGGTTATCAAAGAGAAGTGGGCACTTAAACGGCAGCTTTTCTTTCAGAATAGGGTTTTTATAGGTACCTCAAGTTGTCTGCATTATCTGTGTTATTCTCTGTGTCTTTCTAG
Seq C2 exon
AATGATCTCCATCGTGCCATCCAGCGCACACACTCTGCCATGTTCAACCAGGTCCTCATCCTGATCTGTACACTGCTCTGTCTGGTCTTCACCGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000104868:ENSDART00000161567:6
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:
NO
A:
NA
C2:
PF0788511=Ion_trans_2=PU(11.4=25.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
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]