Special

HsaINT0030829 @ hg19

Intron Retention

Gene
ENSG00000177675 | CD163L1
Description
CD163 molecule-like 1 [Source:HGNC Symbol;Acc:30375]
Coordinates
chr12:7556131-7559448:-
Coord C1 exon
chr12:7559128-7559448
Coord A exon
chr12:7556452-7559127
Coord C2 exon
chr12:7556131-7556451
Length
2676 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
3' ss Seq
TCTCTGTGACTTCATCCTAGATG
3' ss Score
7.02
Exon sequences
Seq C1 exon
ATAGTAGTGATCTTGAACTAAGGCTTGTAGGTGGAACTAACCGCTGTATGGGGAGAGTAGAGCTGAAAATCCAAGGAAGGTGGGGGACCGTATGCCACCATAAGTGGAACAATGCTGCAGCTGATGTCGTATGCAAGCAGTTGGGATGTGGAACCGCACTTCACTTCGCTGGCTTGCCTCATTTGCAGTCAGGGTCTGATGTTGTATGGCTTGATGGTGTCTCCTGCTCCGGTAATGAATCTTTTCTTTGGGACTGCAGACATTCCGGAACCGTCAATTTTGACTGTCTTCATCAAAACGATGTGTCTGTGATCTGCTCAG
Seq A exon
GTAAGACTTACATCCACATGATTACATCAGATAAAATTTCTTTTTTGGAGAACTAGGACCAAACCCTGAAAAAGTTACAACCAATTGTGATGTGTAAGAATTGTGAAGAAGTTACAACCAATTGTGATGTGTAAGAATTGACACTTTCAATGTTTCCTTAGGGAACATGTCTGCATTTTATGCAGCATATTACATTGTAAGCCTCATGGGAATAAGGTTTTTACCCACCCCCAACACACCATTTTACTTAATTCTAATTGGTGCAACAAAATGTCCAATCTAGTCAAAATTGCTGTTAATCTATACAAGTGCATGGCTTATATTAATATTCAGTATAATTTTAAAATGTGTAATCACTTTGCATATTCATAGACACAACTATATTTTTCTAGGTTATAACTGAGTTTGTTTTAGCACTTCCTTTCATTAAAATAAACTATTTCCAAAGAGTACCTATCTAAAAATTTATGACTTTGCTAATTACTTTGTACCTTATACTAGTAAAATTTTTGTCTGCAGCCATTTGTTTTCTAGTTTGCAACTTTCAACTACAAGCAAGTTACCCCTCGCTGTTTATTTATAGTTTTGTATATCAGGGATTAAAATATCCTTCATATTTCTCTCACAGTAGTATTTTATGTTCAAAGATGTAATGAAACCTGTTCACTCTCTTAATAAGATTAAACCCACACCTTCTAATATTCTTACGAAAGGAGAATCCCTAGATGTAGAGCCAACGATTTTCCTCTGAGAGTCAGTTTGTCTTGATGGAAGAGGCTTCTTTCGTAAATTATTACTGACCTTACGTTACCAGCCTTACACAGGATGCCTTAATCTTATTTCCTATAGAATTTGAGATCAGGTCACATCTTTTAAGAAGAGTTTTTCTTAAGTCTAGAGTATGCCGCAGGGAACGATATACATAGAAAAACATATGTAGACGAAGAGGTTTATGGGTTTAGCTGTACCTTAGCCACGGGATTTATGCCATCCTTATAGGACTTTTGGGAAAGATAATATATTCAGAACATCTTTTAATCCTTTTCTTTCTGTTTATACTAGTTTGCTTGCAAGTTTTATCTGGGGACCAACCACTTTCACCATTCAAAAGAGTTTCCCATAGTATATTTAATCAATCCATCATTTTATAAGAAAAATTTTTCTCCACATAACAGAAAAGAGAGGTAGACGAAAGTTAGGAGAGAAAAGAGGGAGACATGAGAAGATGAGAGAGATGAGAGAAGGGGGAAGGAAACAGAGAGAATCTTAATCATTTTGATAAATTTTCTTACAATGAAGTGAATTCATAACTGTGTACTTCTGACTTGATATAACATCCTTAACTGTCAGACCAGTTGCTATTCAAACTCTGGAACTTCTGGAACTATTTGCCTCTGGAAGAGTAAGGAAGGGCCATGAAGAATGATGCAGATGTGAAAATAAGGTTGGAAAACCGTCCCAACAGTGAAAACAGATGTGTATGGCCAACCCACAGGAAAATGGGTAGTTAGATACATTGGCCTTCTCTTCAGCCCTGTAGTCAGAGGATTTTTTTTTCCCAAACAAAAACAGTTCACAGTTTCACAGTTTAAAATCTGTCACTTGATAATTATGTGACCCTGTATAAATCAATCTCCAAGTTGCAGATTTCTTATATCATGACTAGGATAACAGCATTAAATAAAATAGTGCAGGGAAAATACCTAAAATGTGCCTGGCAACCAGGAAGTTCTCAACAGGTATAGGTTGAGAACTATCATTATGACCTACATTATTTATAGGAAAATAAACCTCCAAATCTCCGAAGACTAACCTATTCAATGTGAACCAGATTTCTCACTAGATAGCAAATTATATTTTTGTAATGATGTATGAAAAGCTTGAATAATGGGAGGAGATGAGACATAGAAATTATATCTCCTTTCCTCAATTATTTCAAGAAAAGTTCTCCACATTTTTACTTTCTTGGGGTTATTTAATATATTTATTTGTATGCATGAAAAAGCAGAGTCACAGGAACACAAAGAAGTAACGTGATGTATATGCTGATGGAGCAAAAACACACAGTTTCTTCAAAAATTACCACTGAACAAATTTCATTTCCTATGACAAATATGTTTAATAAGCAAAGGCTTGCTTCTTCGTAGAAAACAGTATGAGAAAGAACATATTTCTATTTAAATCCAAGAGAGACTTTTTGCTAATTGTGCATTCCTTTTGTCCCTTTTCTTTCTGAAGTTACTGAAATGCAAGTATTTCCCAACACTATTTTATTTTACGGTGTTAAAAATAACCACTCTAATATTTTGAAAATTAATGTAATTAATGATATATAGGTTTATATGGCTTTTTATTGCAATGTTTAGTTTCTTAAATTTTAGTAAGGCTAAAGCAAGGTTCTTAGGATTATAATTTCAATTTTCATATTTAAAAGAAGATTGTTTTCATAAAGACTGACAAGTCGTTATGAAACAATCTTTAAAATTTCAATCTTTAAAATCTTTAAAATTTCAATCTTTAAAATTTTAAAACAAAATGATTTCCAGTCTTTAGTCTTTACTTTTCTCAGTATGTGAAGGATACATCTAATCTTCACATTGGAGGGGTTGGAGGAGAGGGATGCTGATGATATTGTCCCAAACCCAATTCAGACGTTTCTCTGTGACTTCATCCTAG
Seq C2 exon
ATGGAGCAGATTTGGAACTGCGACTAGCAGATGGAAGTAACAATTGTTCAGGGAGAGTAGAGGTGAGAATTCATGAACAGTGGTGGACAATATGTGACCAGAACTGGAAGAATGAACAAGCCCTTGTGGTTTGTAAGCAGCTAGGATGTCCGTTCAGCGTCTTTGGCAGTCGTCGTGCTAAACCTAGTAATGAAGCTAGAGACATTTGGATAAACAGCATATCTTGCACTGGGAATGAGTCAGCTCTCTGGGACTGCACATATGATGGAAAAGCAAAGCGAACATGCTTCCGAAGATCAGATGCTGGAGTAATTTGTTCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000177675-CD163L1:NM_174941:5
Average complexity
IR-S
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:
PF0053013=SRCR=WD(100=90.7)
A:
NA
C2:
PF0053013=SRCR=WD(100=90.7)


Main Inclusion Isoform:


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