Special

HsaINT0188694 @ hg19

Intron Retention

Gene
Description
zona pellucida glycoprotein 3 (sperm receptor) [Source:HGNC Symbol;Acc:13189]
Coordinates
chr7:76062244-76062964:+
Coord C1 exon
chr7:76062244-76062347
Coord A exon
chr7:76062348-76062786
Coord C2 exon
chr7:76062787-76062964
Length
439 bp
Sequences
Splice sites
5' ss Seq
AGGGTAAGA
5' ss Score
9.21
3' ss Seq
CAGCTGACTGTGTCTTTCAGAGA
3' ss Score
6.56
Exon sequences
Seq C1 exon
GCAGGGCAATGTGAGCAGCCAGGCCATCCTGCCCACCTGGTTGCCCTTCAGGACCACGGTGTTCTCAGAGGAGAAGCTGACTTTCTCTCTGCGTCTGATGGAGG
Seq A exon
GTAAGAGAAGAAGGCTGGGTGGGACATCTGTGGAAAGACCTGGGCCATCTCAGACCCCTGCCCTTGGCTGTGTCTTTTTTTTGTTTGTTTGGTTTTGGTTTTGGTTGGTTTTGGTTGGTTTTGGTTGGTTTTGGTTGGTTTTTGAGACAGTCTTGATCTGACCTCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAGTCTCCACCTCCTGGGGTTCAAACGATTCTCCTGCCTCAGCCTCCCGAGTAACTGGGACTACAGGCTTCTGACACCACACCCAGCTAACTTTTCTATTTTTAGTAGAGATGGGGTTTTGCCACGTTGGCTAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAGGTGCTGGGATTACAGGCATGAGCCACCATGCCCAGCTGACTGTGTCTTTCAG
Seq C2 exon
AGAACTGGAACGCTGAGAAGAGGTCCCCCACCTTCCACCTGGGAGATGCAGCCCACCTCCAGGCAGAAATCCACACTGGCAGCCACGTGCCACTGCGGTTGTTTGTGGACCACTGCGTGGCCACACCGACACCAGACCAGAATGCCTCCCCTTATCACACCATCGTGGACTTCCATGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000188372-ZP3:NM_001110354:3
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.023 A=NA C2=0.019
Domain overlap (PFAM):

C1:
PF0010018=Zona_pellucida=FE(13.9=100)
A:
NA
C2:
PF0010018=Zona_pellucida=PU(47.2=98.3)


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:
CAGGGCAATGTGAGCAGCC
R:
TGGAAGTCCACGATGGTGTGA
Band lengths:
278-717
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains