HsaINT0184432 @ hg19
Intron Retention
Gene
ENSG00000146839 | ZAN
Description
zonadhesin [Source:HGNC Symbol;Acc:12857]
Coordinates
chr7:100345947-100348519:+
Coord C1 exon
chr7:100345947-100346093
Coord A exon
chr7:100346094-100348247
Coord C2 exon
chr7:100348248-100348519
Length
2154 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
3' ss Seq
TGTTCCCTTCCTTTGCCTAGGGG
3' ss Score
8.67
Exon sequences
Seq C1 exon
AGGGTTTTCCTCAGTGTGACTTTGAAGACAACGCCCATCCCTTCTGTGACTGGGTCCAGACTTCCGGGGATGGTGGACACTGGGCCCTCGGACATAAAAATGGACCCGTCCATGGCATGGGCCCTGCGGGAGGTTTCCCTAATGCAG
Seq A exon
GTGAGGAGATTGAGGAGCGCTCACGCCAAGAAATCACTCAGTCTGCTCCCAGGTAGCAGGCTGGCTGCTGTGACTGATGGGAGACGTTGTTTCAGGCAGTGGGAAGATCAGTCCACAGGTGTTTTTTCGGAAGTTTCCATGGTACTGGAATTGTGGAGATAGCAGAGTAACTTAAAGATTCTCAGGGCTGGGGGGTCACTGAAATCCTGAGAAAACCCAGGCATCTCACTTCATGGAGCCCAAAGCTTCAAAACCCACCACCTCATTTTCAGTCTAGACGTTTATGAGTGGCTCATGCCTGCAATTCCAGCACTTTGAGAGGCCGAGACGGGAAGATTGCTTGAGCCCAGGAGTCTGAGCTCAGCCTGGGCAACATAGTGAGAACCCCATCTCTAGAAAAAAAAATTTTTTTTTAATTAGCTAGATGTGGTGGTGTGTGCTTGTGGTCCCACCTACTTGCGAGGCTGATGTGGGAGGATCGCTTCAGCTCAGAAGTCAAGGCTGCAGTGAGCTATGATTGAACCAGTGCACTCCAGCCTGGGCAACAGAGCAAGACCTTGTCTCTAAAAATTAAAAATAAAAAAATAGGCCAGGCATGGTGGCTCACGCCTTTAATTCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGAGACCAGCTGGGCAACATAGTGAAACCCTGACTCCACTAAAAAAAATGTAAAAATTAGCCGGGAGTGGTGGCGTGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAACTGCCTGACCCCAGGAGGTGGAGACTGCAGTGAGCTGAGATCGCACCACTGCACTCCATCCGGGGCAACAGAGTAAGATTCTGTCTTAAAAATATATAAAAAGAGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGAGGGCGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCCCTACTAAAAACACAAAAAATTAGCCAGGCATGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAGCCCGGGAGGCAGAGCTTGCAGTGAGCCGAGATCACGCCATTGTACTCCAGCCTGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAAATATATATATATATATATATATATACACACACACACATATATATACACACATATATATATACACACACACACATATATATATATAAAGAAATAATTTTTTAAAAAGACAATAATGAGGGTGGGGTGCAGTGGCTCACACCTGTAATCCCAATGCTTTGGGAGGCTGAGACGGGTGGATCACTTGAGGCCGAAAGTTCAAGACTAGCCTGGCCAACATGGTGAAACCCCACCTCTACTAAAAACACAAAAATTAGCCAGACATGGTGGTACACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGACAATCGCTTGAACCTGGGAGGTGGAGGTTGTAGTGAGCTGAGATCGTGTCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAACAACACACACACACACACACACACACACACACACACACACACGACATTAATGAATGTAATCTAGGTTGCTGGTTTGTTATTCCCTTTTTTTCTTTTTTGAGATGGAGTCTTGCTCTGTTGCCAGGCTGGAGTGCAGTGACGTGATCTTGGCTCACTGCAACCTCCACCTCCGGAGTTCAAGCAATTCTCCTGCCTCAGACTCCCGAGTAGCTGGGACTCCAGGCACGGGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGATGGCCTTGATCTCTTGACCTCGTGATCCGCCAGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCTGGCCGCTTTTCCCTTTCTTTGTGATCCCACCTTCTTTAGTTAGATGTCTAAAATGAGCAGAAAAAATAATGCTACGACCTGGGAAATTTGAGTGTTTGCTCAGATTCCCGTTCAGAAAGCAAAGCTTTGCTAAAGCAGCAGTTGGCATGTCCTGTGCAGGCTTCTTACCTTGCCTGTTCCCTTCCTTTGCCTAG
Seq C2 exon
GGGGTCACTATATCTACCTTGAGGCTGACGAGTTCTCCCAGGCAGGCCAGTCAGTCAGACTGGTGAGCCGGCCCTTCTGCGCCCCAGGTGACATCTGCGTGGAGTTCGCATACCACATGTATGGCCTTGGGGAGGGTACTATGCTCGAACTCCTCCTGGGAAGTCCTGCGGGGAGTCCCCCGATTCCTCTCTGGAAACGCGTGGGGTCTCAGCGCCCTTACTGGCAGAACACCTCCGTCACCGTCCCCTCAGGACACCAACAGCCCATGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000146839-ZAN:NM_003386:11
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
No protein impact description available
No structure available
Features
Disorder rate (Iupred):
C1=0.220 A=NA C2=0.121
Domain overlap (PFAM):
C1:
PF0062918=MAM=PD(0.1=0.0),PF0062918=MAM=PU(26.8=88.0)
A:
NA
C2:
PF0062918=MAM=FE(54.9=100)
Main Inclusion Isoform:
NA

Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Conservation
Rat
(rn6)
No conservation detected
Chicken
(galGal4)
No conservation detected
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
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]
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)