Special

HsaINT0090527 @ hg38

Intron Retention

Gene
Description
laminin subunit gamma 2 [Source:HGNC Symbol;Acc:HGNC:6493]
Coordinates
chr1:183220825-183222211:+
Coord C1 exon
chr1:183220825-183220961
Coord A exon
chr1:183220962-183222088
Coord C2 exon
chr1:183222089-183222211
Length
1127 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAG
5' ss Score
9.06
3' ss Seq
TGATTATGTTTGTGTTCCAGATG
3' ss Score
10.91
Exon sequences
Seq C1 exon
GTGTCGATCAGGTTACTATAATCTGGATGGGGGGAACCCTGAGGGCTGTACCCAGTGTTTCTGCTATGGGCATTCAGCCAGCTGCCGCAGCTCTGCAGAATACAGTGTCCATAAGATCACCTCTACCTTTCATCAAG
Seq A exon
GTAAAGCCTTCTATTTTCTAGGTTTTAGTTTTTTAATGTTGTACAGGGCTTTGTGTTTAGAGACAACCACCTCCGCATTCACAGGATGGATTCTCTTTAGAAATTCTCTTATAGTATTGAATGTACATTATTTTGTCAGGGCACTCAGGCATATCCTGATGTCTTGAAAAAGTCATAGGCTGAAAATAGTTCATTCATACTAGTGAATATAACTTAAAAGAATAACTAAAAAAGAGACTAGATTTTTATTTCCCTGAATTTTCCATCCCCATCTATTTCAAAACCACGAAGGAATCATTCATTTGGTTTGGAGAGTGTATGAGTCTTCCTGGAATTCACGTTCACTAATAATGCTGTTTTCACATATAATAAATGAGCTGATTTATGTGAAATTAGTTCCCAAGCTACAGAACACTATAAAAATATTGGAAACTGATATTATTTCAACATTAAGTCTGAGTTTCCCTTTGAAAAGACTGGACCCGGGCCAAGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGACAGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCCCTACTAAAAATACAAAAAAATTAGCCGGGCGTAGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCGTCTTAAAAAAAAAACAAATGAAAAAAAAATGAAAAGACTGGACCCTCTCACTTCATTAAGGTGAGAGCTTTTTATATAAATACAAAAAAATGCAAATTACAGGCAGAAGAAAACCTGCTATCTTATCACGAGTCAGACTCAAAGATGAGAAATCATAGCAGCTGCGGGATGGGAGCAGGTGAAGTTGAGAGCCACATAGAGAGATACATGCAGAATTTTAAGGACCATTTGCAAATGTGGAAATATTGAGAAAACCCCACTTTCTACTCACCACTAGGACTTGTCGGCAAGCAAATCTTTCTTTGTTTAACTTAATAGATGATGAGGGCTTGTCCAATGCAGACTGATTATGTTTGTGTTCCAG
Seq C2 exon
ATGTTGATGGCTGGAAGGCTGTCCAACGAAATGGGTCTCCTGCAAAGCTCCAATGGTCACAGCGCCATCAAGATGTGTTTAGCTCAGCCCAACGACTAGACCCTGTCTATTTTGTGGCTCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000058085:ENST00000264144:5
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=0.024
Domain overlap (PFAM):

C1:
PF0005319=Laminin_EGF=PD(34.8=34.0)
A:
NA
C2:
PF0005213=Laminin_B=PU(3.8=11.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATCAGGTTACTATAATCTGGATGGGG
R:
CAGGAGCCACAAAATAGACAGGG
Band lengths:
254-1381
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