Special

HsaINT0003350 @ hg19

Intron Retention

Gene
ENSG00000135503 | ACVR1B
Description
activin A receptor, type IB [Source:HGNC Symbol;Acc:172]
Coordinates
chr12:52374753-52377950:+
Coord C1 exon
chr12:52374753-52374983
Coord A exon
chr12:52374984-52377782
Coord C2 exon
chr12:52377783-52377950
Length
2799 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGG
5' ss Score
10.51
3' ss Seq
TCATCTGTGGTTCTCTGCAGATA
3' ss Score
11.24
Exon sequences
Seq C1 exon
GGTTACCCCTCTTTGTCCAGCGCACAGTGGCCCGAACCATCGTTTTACAAGAGATTATTGGCAAGGGTCGGTTTGGGGAAGTATGGCGGGGCCGCTGGAGGGGTGGTGATGTGGCTGTGAAAATATTCTCTTCTCGTGAAGAACGGTCTTGGTTCAGGGAAGCAGAGATATACCAGACGGTCATGCTGCGCCATGAAAACATCCTTGGATTTATTGCTGCTGACAATAAAG
Seq A exon
GTAAGGGCTGGGCTTGGATACAGCATTCCCAGATAGAGGATGCTAGAGAAAGTGCATAGCTATGGGGTGCACAGCTCTGTTTGCCTTCATCATTGTAACCCGTAGAAAGAAAACTTGAGTAAGGTCAAGGTTTCCATGCTTTCCTTAAAGTGTGGAGCCTTTTATTCCATGAAAAGGTTATACAAAAATCCAGGTTATCAAGCAAATAAACAAGCAGTTCTTACTCAGATAAACAAGATACACCCCCTCACCCTACCTGCTCAATTTCTCTTTCTCCACTCCCCCAAACCCACCTCCATTGTAGTTCCTGCAGGGGGTCCCGTAAGCTTATTTTGAAAATCACTAGGATGGGCTGGGCGCGGTGGCTCACGCATGTAATGCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACTTGAGGTCAGGAGTTTGTGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAATACAAAAATGAGCTGGCCACGGTGACACCTACCTGTAATCCCAGCTATTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGGAGGTTGCAGTGAGCTGAGGTCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAGAAAAAAAAAATCCCTAGGATGAGGAATTGCGGCCTCAACCCTGGCAAGGAGGATAACGACAGAAAAGCCTGTAGTCCACGAAGTGTCGCCTTCGGACTCTGCTCTTGGTCAGTCCTGTCCCTGAGGATTCTTTCCTTCTTCCTCTCCCTTTTATTGCTTTAGTTTTTGAATCTCTTATGTGCCAGGCACCTCCCTATGTTTGAGGACCTCATTGACTAGCAAAGGATGACGAGTAAGGGTGATTAGAGGAGGTAAACACGAGTTGTTCTGTTGAGCACAAATTGGGGCTGACTCGCACCTGAGCCCAGTTGAGACAAAGGTGGCAAGAACTGGTCAGGAAGAAAAATCTTCCTTGCAGGGAAGAGCACTGCAGACATGTGCAAAGGTGAGGTTTGGGGCCCAGCAAGTAACTTGGATGGCTGTGGGTGGAGAGGGAGGCAGAGGCCAGATTATGAGGGGCCTTTTTGAGAGGATTGTATTCCATTCTGAAGATAGTGGGTAGTAATTAAAATTTCATTCATTAATTCTATAACATTTATTGACTGCTGTGGGCCAGACCTCTGCTGGCTGCTTGGACCATCACACATAAGAGCAAGACACAGTCCCTCCCCTCACAGAGCTCCCAGGAAGAAGGGGACAGACACGTGGACAGGTAGTGGCACCCGGAGCACAGAGAGGATGCTGTGAGTGGCTGGTTCACATTGTGGAAGGGTCTCTCTAGCAGTTGTGACATGACTTGCTCCTGTGGCATGGTGCAATTTAGAAGTTAGTGTCTACAAAGCCTACAGAAGATGCTATTTGTTTTTCATTCCTGAAACAACAGCAGACTGCTCATTCCTCACATTGCCATGGGAAGTTGTAATGGTCTCTGCTGCCCCCAAGCTGAGGAGCCTTAGACTCCAATACAAGGGAGGAAGGGGAAGAGCAAGATTTTTATTCCCACTGAGTAAGCTATTCCTTTTTAAAACTATCACCTTTTGATAAAATTTAAATCTTATATGTTTTAAAAGGATCAAATCATGTCTTCTCTTTGAACTTGTTAGCAGGGTCCTCAGGACTTTGGGGCTGGTTAGAGTGCGAGAAGCAGTGTGTTGGGTGGGCCCCTTGTTTGTGATAAGAGAAGCCAAGATGTGTGTGTTTCCAGGATCCATCCCTTTATTGATTCTGGCAGCTTGTGTGAGTAGGGATCTGGCTTTCAAAACCCACCTTAAGGCCAGGGAAGGGAAACAATCAGACTCCCTCGTTCTTGCCTTTTTAACATGGGGTATATATAGTATGGTGCCCTGGAATCAGCGCCAGCCTGGAATTTTGGAGATTTCAACTCAATTTCCAGTCTTCCAATTGACAACGGCATGGCTTAATTCGATTCCTGGCTTTGGTGTTTCTTTTTCTCCCTCCTCCTGCTCTCCTCCTTCCTGCTGTCCCTAGTGTAAAAGAGAAAATAAAGTGTATGCACTCTACCTTCCATTGCTCCTCTGAAGGATGAGATGCCTTTCTGGGAATACTTGGAAGTGGTCTATTCATGCACTGAAAAGCATTTTTTGGCCTGGAATCCAATAATCCATAAAGGAGATCTTTCCTACTCACAGAGATATCATAGCCTGGTAAGAACAACAGACTGAAAAGAAACATTACAGATGAGACAGGTGCTGTGTTTGGGCTGTGTTCAGAGGGTCGCTGGGACACAGGAGGCCCTCCAAGGCTTTCCTGTTTGGTGGTGGTAGATCCAGCTCATTGTGGTTCTCCCGTGCAGATGAGCAAGTCTTGGTCAGGATCAAAGCAGTGCTGCACACAAAGCTGGTGATAGCTGTTACCTTCCCCAGGCATATGCCTCCTCTTTCCTGAGTACCTCACATTTCAAATTTGACATAATGTTCAGAATCCTACAGTTCACCTAAAGGAAATCAGGAGCAGTCCTAAGAAAGAAATGGTGTTCCCCTGTCCTTACTGAGGTCCCAAACTGGTAGACCACTATAAATGAAAGGATGCTAGATGGGGCTTCAGGGGGCATGGAGGTGGGAAATGTGAATTCAGGAGTCTAACCTGATTTTGTGTTGTATACACTCATCCTTACCAACCTTCACTGTTTTGCTGATAGTTACACTTTTTCTGGGACTCATCTGTGGTTCTCTGCAG
Seq C2 exon
ATAATGGCACCTGGACACAGCTGTGGCTTGTTTCTGACTATCATGAGCACGGGTCCCTGTTTGATTATCTGAACCGGTACACAGTGACAATTGAGGGGATGATTAAGCTGGCCTTGTCTGCTGCTAGTGGGCTGGCACACCTGCACATGGAGATCGTGGGCACCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000135503-ACVR1B:NM_004302:4
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:
PF085157=TGF_beta_GS=PD(37.9=14.1),PF0006920=Pkinase=PU(22.2=82.1)
A:
NA
C2:
PF0006920=Pkinase=FE(19.4=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:


Other Skipping Isoforms:
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
  • Pre-implantation embryo development