Special

HsaINT0038916 @ hg19

Intron Retention

Gene
ENSG00000187498 | COL4A1
Description
collagen, type IV, alpha 1 [Source:HGNC Symbol;Acc:2202]
Coordinates
chr13:110861739-110862389:-
Coord C1 exon
chr13:110862327-110862389
Coord A exon
chr13:110861775-110862326
Coord C2 exon
chr13:110861739-110861774
Length
552 bp
Sequences
Splice sites
5' ss Seq
CCAGTAAGT
5' ss Score
9.09
3' ss Seq
TAAAATGCTGTCTCTCCCAGGGT
3' ss Score
8.92
Exon sequences
Seq C1 exon
GGCCCACCAGGACTGCCAGGGCTTCAAGGTCCTGTTGGGCCTCCAGGATTTACCGGACCACCA
Seq A exon
GTAAGTTTTGGGGGCTGTCTCTCCGAGGCAATCATTTAAAAAACAACTATATTGAGGTTTGAAAATAAATAATAATTTAGTAAAAACTTTACACAGTTGTGGTCGCTCTTAATTTGGACATGGCGGAATCAGCTTCCCTCTTACTAAACGTTTGGCTGGCATCCCGGTACCCATATACCCAGAGCTGTGGGAAAGGGATGATGATAGTACCATAAACTGATACCCTGAAACAAATAATGCAGTCATGGTTGAAGGGGCTGGCGGGGTACTGCTGATAGTCACAGCCTGTGGGAGTGAGTTCAAAGATGGACAGACAGGCTGTGCCCCAGGTGACTTCACCAGGGAGCAGGGGAGATGGATTGGTATTGGTATGGTCACACCTGAGGGTCCTGCACCTGCTAGGAGTGGGGAGGGAGGGGAAGCCCAGGAAAAATATTTCACAAATAAATTATCATGTTGACCAGAGAATCTTAAGATAACGTCAGCCTGAAGAAGGGCTTAAAGCTCCCTAGAGTTCTGAATCCTATTTAATTAAAATGCTGTCTCTCCCAG
Seq C2 exon
GGTCCCCCAGGCCCTCCCGGCCCTCCAGGTGAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000187498-COL4A1:NM_001845:10
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=1.000
Domain overlap (PFAM):

C1:
PF0139113=Collagen=FE(33.9=100)
A:
NA
C2:
PF0139113=Collagen=FE(18.6=100)


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:
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