Special

HsaINT0000669 @ hg19

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 4 [Source:HGNC Symbol;Acc:34]
Coordinates
chr1:94510169-94512649:-
Coord C1 exon
chr1:94512475-94512649
Coord A exon
chr1:94510301-94512474
Coord C2 exon
chr1:94510169-94510300
Length
2174 bp
Sequences
Splice sites
5' ss Seq
CTTGTGAGT
5' ss Score
7.15
3' ss Seq
CTGACGCCTGTGTTCTGCAGGTC
3' ss Score
9.61
Exon sequences
Seq C1 exon
ACTCCTTCTTTGAACGTGAGCATCCAGGGTGGGTTCCTGGGGTATGCGTGAAGAATCTGGTAAAGATTTTTGAGCCCTGTGGCCGGCCAGCTGTGGACCGTCTGAACATCACCTTCTACGAGAACCAGATCACCGCATTCCTGGGCCACAATGGAGCTGGGAAAACCACCACCTT
Seq A exon
GTGAGTCTTCCAGCAGAGAAGCTGGCTGCCATGCTAGCCTGTCATTTCCTGGCTTAGTCTTTCCCTATCAGCGGCTGTCTACTCTTTCCCACAAATTTTAGTGACAAATATTTGCGGCCCCAAAAATGTGTAAAAGCTTTCTGCAGTATTCAAAGATCACTAATATGTATTCTCTTGATGGGGAGGTAGAATACGTTTATTGCCCCTTTTGTGTGCCGGGGAAGTGGACATTCATTCAGAGAGTTGAAGTGACTTTCCTGAAGCCACCAAGTTGTCATGGCTCAGCGGGGGCAAAAGCCAGGCACCACAGTTGCCTCTTGTTTCTCACACCTTGAGTCTTTCCCCCCATCTCAACAGTCCATGGTGGTGATCAAGTCATGGCCACTGTCATCATGTGCATGGAAGCTATAGAGTCCTCCTATTTCCTTTCTCTTTTCTTTTCTTTTTTTTTTTTTTTTTTTTTGAGATAGTAACCATTACCCATGCTGGAGGGCAGTGGTGCGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGATCAAGCGATTCTCCCACCTCAGCCTCCCAAGTAGGTGGGACTACAGGTGCATACCACCATGCCCAGCTAATTTTTGTATTTTTTTTTTTTTTTTTTTTTTTTAGTACAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCTTCCCAAAGTGCTGGGATTACAGGCGTGAGCGACCGCACCAGGCCGAGTCCTGCTATTTTCAAGGAACATTCCTTTTCCTACCAATCATTAGGCAGGCTTCAACATCAGCTGATGAGGGTTAGTGGTCGTTCTGGAGAAAGTGAAAAAAGAATCAGTCTCTAGAGGGGCTTGTGGAGTAACCGCCTGGTAACAGAAGGTCAGGGCAGGGAAGGCAAAGGGGCTCTGCGCGGATCTCTCAGCTCCGCAGGCGCCCCACTCTCCTCCAAGGGACCCGAGCGCCATCTGCTGAGAGGAGAACACGGCCCGCCATGGTTTCCCAAGGAGCAGCAGACACGGACCTCGCAGGGGGCAGCGAACCCACGTGACACAGTCTTCAAGTCCTTTGGAGAGCCCCAGGAAGGAACAACAGCGTGTACACCCTGTGATGGAATGTTCTCTAGGGCGGTTCAGTGTGAATGGAATGTGGGGCCGGTGCCATTCTAATTGGTTCTGTTTCCCTCTAGTGGTTGATCGCGGAGATTTCGGCTTCTCCATCAGGACAAGTTCAGATAGCCTGAGATGGTATCAGAACTCAGGGACAGAGCTGGGTGTGGCGGCCCTGCATCCATCTGCTTTCTCTCCATGCTAACTGATATGGTCAGAGAGCTGGAAGCAAATTCCAGGACCCCAGGGCTCCGCAAAGGCAAACACATTACTTCATCGGCTGCTGACATGCAACTTCCCCCAGGGGTTAAAACAATGTTTAATACTAACAGTAATAATATTTTTGAGTTTTACTTTATGCTGGCGCTGTTCTAATGTTGTAAGTGTATTAACTCATTTAAGCCTTACAACAACCTAAGGACATGGGAGTCATAGTTCCCATTTAAAAAAAAAAAAAAAAAAAGCCCACCATTGCTCTGAGGCTTTTTATGTTTTGGATCCAAAGCTAATATTGGTGGTGGTAATTCCCATGCCTGGCTTCGATCAATTAATCAGCAAATGCCTAGGACTGCTTAGGGTTCTGGCCTTCATCAAGACCTTACCCGGGCTTTATGATGATGACACCTGGCTTTTCAATAGCCATGACTGCTCACCCAGGAGGCAACGCCTCGAGTCATGCACCGAACACCTTTTATTGATCCTCTCCAACACCAGGCTCCGTGATGGCTGAGCTGGGGACACCTGTGACTGCACGTGAACATTTTGAGGCTGGGAATCCCAAAGGCCCTCGGCGTTGGCCTGGGAGCACCATGAAACAAGTAGAAGCAGAGAAGGATGGCAGAGGTGGCCCTCTGCATTAGGGCCTGGATGTATACACTGGTGCTAAGGGGGCCCCACAGCTAATAGGGGTTTGAGTTTGACTGACAGCCCCAGGCAGGAATCTGTGAGAGTTCTCACTGAACCTGGTGTGGGGGTGGCCCTCCTAAGGCATGTTGCTAAAGGCCATCTCTTCTGCCACTGACGCCTGTGTTCTGCAG
Seq C2 exon
GTCCATCCTGACGGGTCTGTTGCCACCAACCTCTGGGACTGTGCTCGTTGGGGGAAGGGACATTGAAACCAGCCTGGATGCAGTCCGGCAGAGCCTTGGCATGTGTCCACAGCACAACATCCTGTTCCACCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198691-ABCA4:NM_000350:19
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.034 A=NA C2=0.089
Domain overlap (PFAM):

C1:
PF0000522=ABC_tran=PU(18.6=45.8)
A:
NA
C2:
PF0000522=ABC_tran=FE(30.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development