Special

HsaINT0035188 @ hg19

Intron Retention

Gene
ENSG00000101204 | CHRNA4
Description
cholinergic receptor, nicotinic, alpha 4 (neuronal) [Source:HGNC Symbol;Acc:1958]
Coordinates
chr20:61987723-61991051:-
Coord C1 exon
chr20:61990900-61991051
Coord A exon
chr20:61987768-61990899
Coord C2 exon
chr20:61987723-61987767
Length
3132 bp
Sequences
Splice sites
5' ss Seq
GTGGTAGGT
5' ss Score
7.23
3' ss Seq
TTCCTCTCTCGGTGCCCTAGGAT
3' ss Score
9.61
Exon sequences
Seq C1 exon
CCAGCAGCCATGTGGAGACCCGGGCCCACGCCGAGGAGCGGCTCCTGAAGAAACTCTTCTCCGGTTACAACAAGTGGTCCCGACCCGTGGCCAACATCTCGGACGTGGTCCTCGTCCGCTTCGGCCTGTCCATCGCTCAGCTCATTGACGTG
Seq A exon
GTAGGTGAGGGCGTGGCCATCGTGCACTGTGACTGAGGTCGCCCTGCAAGGAGCACAGGGGTCTGGGTGGGCAGAGGGGACACAGCCATCAACACTCCCCGTGGCTGTGAGTGTCCGGCCCGGGCTGGTACGTCAGAACGACAGCCACCAGCTCTGCCCCGCCTGAGCCCCAGCCAAGGGTTGATTCAGAGCGTCCCAGCCAGGCCCTGCCCTTTCCTCCCCCTTGACGTGGGAACACTCCAAGTGGCCAGGTTCTCAGTACAGAGCCCAGGCACCTTCGGAAGCAAAGAACAGCAAAGGCCTTGCTTGGGGGTGGCGGGGCACGCTGTGACCTCGGAGCAACAGGGACAACCGGCCGGGGCAGGGGCCGGGGCAGGAGCAGGCACTGTGGTGTCCCGGCAGCACCCCAACCTTAGCTGGCCCCAGAGGCCCCTCACCCACAGATCTGGAATGTGGGGTTTGGGGGAGTCTTGGGCGAAGTCTGTTTGTCTGAAGATATGTTCTTTCTGGTGGGGGGCCCAAGAAGGCTGCTGGGAGGAAGCCTACTGGTCCAGCCAGGCCCCTGCAGCGTGGGCCAGTGCACATGGAGCCCCAAGGCAGGATAGGAACCAGGAGGCTTCGAGGCTGAGAGAACTGAGCTGCGGGAGGCTCGGCCTTGTGCTCGGTTGAGATGCTTGGTTACCTACCCAGGCCTGAGCCAGACTGTCTGGGGGTCTCGGCGGCCCTGGAGGGGCCGGGTAAGGGGCAGCAGAGACATTTCCACGTTTCCCAGCCAGGCTCAGCCACTCCAAATGGGGTGAGACCATCCCTCAGGGTACCTGGCTGGGTGGGGGTGCATAGCCTGGGGGCTGCCACCATGGAGGAGGGCAGGTTGGGCAGGCCATGGTCTCTGGGAGCTGGCCCACTTGCGAGTGGGCAGCCAATGGCCAGCTGAGCTGCAGGGGCTCGTCTTCCACACTGAAGTCCGCCAGCTCCAGCCCTGCTGCCAAATCCCAGCTCGCTGGTCCAGGGAGGGCACCCCCACATGGGGAGGCATTTGTATGCTGTAGAGGCCCAGCCCACACCTTGCCAGGATGCCAAGCCTGGGTCTGCCGCTGAGGGAGGAGCCACCGGGTTGCGGGAGAATTTCCTCTCTTTGGGAGGCTGGTGCCGTGCGTGTTGGGTAACCCTGGGCCTGGGGCCTGTGAAACGGGGTGAGAGCTGCTTCACTATCCCAGGCTGAGTGGGCCACACCCCAGGGGCTTTTGGGAGGTGTGGGGAGCTGCAGCCACATTCCCGCGGACAGGCTGCTCAGTGGTGGCAGTTGCCCATGCAGGGCAGCGCATGGAGACTCCAGTCAGCCAGCCCCGTCCAGGGTTGGCCACCCAGACCTCCAGCCTCAGTGTCCTGGAGCTGCCCTTGAGTGGCTCCTGTGGAGTGTCCCTGGCGGAGGCCCAGCCAGAAGACAATGCGGGTTGCACAGGCTTGGCAAGCCTGCTGAGGTTTGCAAACACGGCTGCAAAGTGATAGCTGGCAGAGGCGGCCGCTGGCAGCTGCCCAAGGCTCTGGGTCTGCCACCCCCCACCTGGCTGCCTACCTGAGCTTCTCAGGGCTCAATCCATGGCTCCCTACGCCACCACAGAGTCCCCAGTTTGCCCAGGAGACATTGAGGCCTGGAGCACACCCAGAACCAAGACTCCCAGAGCTGCCCACCCCTCTCTCCACCCTGCAGCCGACTAAGGACTTACACGAACATGCACACGTGGGTGCTGACGCTCCTGGGTGCCCAAGGCCGAGGGCCACGTGTGCACGGAAGGGGCTGCCTGATGCTCCTGGGTGCTGGCCTAAGGCTGAGGACCACGTGTATGTGGAAGGGGCTGCCTTGTGTCTGGCCCACTCTGCCCGTCCCACCAGGGGCTGGGGATTCACCTGTGCCCCCTTTGCGGGCTCGGATACTTGTTATAGGTGCCATCACCAGGGTCTGTCCTGGAGGGGAGGGCTTGTGAGCTGCACGTGTGAGCTCAGGCCCCAGGACTGGCTGCAGAGGAGGGTCTGGAAGACCCAGTGCTTTTCCAACCAGCCCAGGCCAGTGCTGAGTGGTGGTGAAATGTGCAGTGTTGACCTGCCCTCCAGCTTCAAGGGCGACTGAGAATGACGGCTGCAAGGGGGTAGGGCACGACACTGGGCAGGAGGGCCAGGCCTGGCCACGTGAAGCTGGTTCTGAGGACCCTGGAGCTTCCTCAGACACACGGGATGAGGTCCTGAGGGGATGAGGTCCTGTGGGGAGATATGGCCCTGCACGGAGACATGGTCTGTGGGGACGTGGTCTGTGGGACGTGGTCCTGTGGGGACATGGTCAGTGGAGATGTGGTCCTGTGGGTTGTGGTCCTGTGGGAATGTGGTCCTGTGGAGACGTGGTCCTGTGGGGACACGGTCCGTGGAGACGTGGTCCTGTGGGAATGTGGTCCTGTGGGGATGTGGTTCTGTGGGGACGTGGTCCGTGGAGATGTGGTCCTGTGGGTTGTGGTCCTGTGGGGACGTGGTTCTGTGGGGATGTGGTCCATGGAGATGTGGTCGGTGGGGACGTGGTCCTGTGGGGATGTGGAAGGAGGTGGGTGGGGTGGGTCGGAAGGGGCTGGGGTGAGTGGCCCAGCTGCACACAGTGACCTTGAGTGACAGGTCCCACCTGCTCAGGTCATGAGGCACAGTCCTGGAGGGGCCACCCTGGCCAGCAGTGGAACCCACTTATGTGCCAGGGGCAGCTTTGCTGGCTGTGTGTGCCCACATGGGGGCCTTGTCTGCAGAGGGGCTGCCCCCAAGGGCCGGGAGGGAGCAAGGCAGGTGGGCAGAAGGAGGCTCCCCATGCCCGCCACACCTGTCCTTAGCTGGGGAAGCCTGTGAGGCCGCCGACTCCTCTCCAGTTTCCTGCTGGAGATGTTTGTGGCCTTGTCCCCACATCCCTAGGTCCCCTCAGAGTCCCCATCCTGGGCTCGGCTGCCTCCAGGGACGGGGCACTCACCCCCTCCACAGGTCGCCCGTCCACCATATCTTGCCCTGGCCGTGTCCTTGTGCCAGTGGCTGTAGATGAGGAAACCTAGGGCCAGAGAAAGACACCAAGGGGTCACTGGCCCCCTTCCTCTCTCGGTGCCCTAG
Seq C2 exon
GATGAGAAGAACCAGATGATGACCACGAACGTATGGGTGAAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000101204-CHRNA4:NM_000744:2
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.029 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0293118=Neur_chan_LBD=PU(18.8=76.5)
A:
NA
C2:
PF0293118=Neur_chan_LBD=FE(15.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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