Special

HsaINT0035215 @ hg38

Intron Retention

Gene
ENSG00000170175 | CHRNB1
Description
cholinergic receptor nicotinic beta 1 subunit [Source:HGNC Symbol;Acc:HGNC:1961]
Coordinates
chr17:7455794-7457707:+
Coord C1 exon
chr17:7455794-7455941
Coord A exon
chr17:7455942-7456582
Coord C2 exon
chr17:7456583-7457707
Length
641 bp
Sequences
Splice sites
5' ss Seq
GCGGTATGT
5' ss Score
9.45
3' ss Seq
TTTCCTTTGCCTACCCACAGCTG
3' ss Score
11
Exon sequences
Seq C1 exon
GTTCCAGCCTGAACTGTCTGCCCCTGATCTGCGGCGATTTATCGATGGTCCAAACCGGGCTGTGGCCCTGCTTCCGGAGCTACGGGAGGTCGTCTCCTCTATCAGCTACATCGCTCGACAGCTGCAGGAACAGGAGGACCACGATGCG
Seq A exon
GTATGTCCAACGGGGGTGGAACAAGGCCAGGTCTAGGCGACCTTGGCCCCACCCCCAAATTCCGCACCAGCACTCGCTTTCGTTTTTTTTGTGTGGTTTTTTTTTGGCTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTCGATCTCGGCTCACTGCAACCTCCGCCTACGGGTTCAAGCGATTGTCCTGCCTCAGCCTGCCGAGTAGCTGGGACGACAGGGGCGCGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGTGGCTTCACCATGTTGGCCAGGCTGGTCTGAAACTCCTGACCTCAGGTGATCCGCTCGCTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTCGCTTTCGTTTCTGATTGGACCTCTCCCTCATTTGGTCCCACCCCCTGCTTACCTACTGGTTCTTTATGCCCATGCATTGCCTGCAGTCTCGCTCTCCTGTTGGCGCTGCCGGCTGTTGCCTCAAACCAGTGGTAGGAGGACTCAAGCGGGTAGCGGGCGGGGAAATGGGGGGGTTTCCCTGGGGGTCTGGGCCCAGAGCTCAGGAAGTTTCCTTTGCCTACCCACAG
Seq C2 exon
CTGAAGGAGGACTGGCAGTTTGTGGCCATGGTAGTGGACCGCCTCTTCCTGTGGACTTTCATCATCTTCACCAGCGTTGGGACCCTAGTCATCTTCCTGGACGCCACGTACCACTTGCCCCCTCCAGACCCCTTTCCTTGAAGACTGGAGGGTTGAGACCCAGGCCCCCTGCCAGTTGAAGTGAGAGTTTGGTGATACTGTCAAGCCCTATCCTTCTCTGCCTCTTAACTCCTTCACGAGGAATCTGGGCCTCTTATTTCGTTTCTGGGGACTGCATTGGACTGAGGGCTGGGTAGGCAGGTGTCTTGGACCCACCTGAAATGCAGTATCATCTGATTTACTCTTTGGGATCTTGAAGAAGCTCTTTTGGGTATCAACACCTAGGTCGCCAGTGAAATAGAACACAGAACAGGAACTAGATTATAAGCCTTATGAGGTCAAGAAATGTGACTTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCCGACCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGGTACATGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCACTCGAACCCGGGAGGCAGAGGTTGCAGTGAGTCAAGATCACGCCATTGCACTCCAGCCTGGGCAACAAGAGCGAAACTCCATCTCAAAAAAAAAAAAGTGTCTTGTTCACTGCAGCATGCCCAGTGCCACGCACAGGTGCTGACCTATAGTAAGTGCTTAACATTTGTTGAATAGGGGAAAGAAATTTCCGGAAGTAAATACAGCAATTAATAATGTTTATAAGCTGGGCATGGTCGCTCAGGCCAGTAATCCCAGTGACTTAGGAGGCTGAGGTGGGAGGATTACTTGAAACCCACAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCCTGTCTCTAAAAAAATAAAAATAGAAATAAAGTAGTGCTTATTGTTTGCATGTTGGGTCTTGTGGTCGTTTTCTTTTTACCTTTCTGTAATTTATTATGTTTTGTAATGTGTACTATCTCTGGGATTAAAAAAAGTTATTTCTA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000170175:ENST00000306071:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0293211=Neur_chan_memb=FE(20.8=100)
A:
NA
C2:
PF0293211=Neur_chan_memb=PD(13.1=66.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCCTGATCTGCGGCGATTTAT
R:
GAGGCAGAGAAGGATAGGGCT
Band lengths:
351-992
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