HsaEX0073860 @ hg38

Exon Skipping

Gene

ENSG00000203326 | ZNF525

Description

zinc finger protein 525 [Source:HGNC Symbol;Acc:HGNC:29423]

Coordinates

chr19:53372342-53384335:+

Coord C1 exon

chr19:53372342-53372396

Coord A exon

chr19:53375770-53375896

Coord C2 exon

chr19:53380722-53384335

Length

127 bp

Sequences

Splice sites

3' ss Seq

AAAATGTGTTTTCATTTCAGGGT

3' ss Score

9.4

5' ss Seq

TGGGTGAGG

5' ss Score

6.74

Exon sequences

Seq C1 exon

AAATGCTGACCTTGGAGTTGGGAATCTTCTAAGTCTGAAGCTTCCTGCCTGACAG

Seq A exon

GGTCTATTGACATTCAGGGATGTGGCCATAGAATTCTCTCAGGAGGAGTGGAAATGCCTGGACCCTGCTCAGAGGACTCTATACAGGGACGTGATGCTGGAGAATTATAGGAACCTGGTCTCCCTGG

Seq C2 exon

GTATCTCTTCCAAATGCACAATGAAGGAGTTCTCATCAACAGCACAAGGCAATACAGAAGTGATCCACACAGGGACATTGCAAAGACATGAACGTCATCACATTGGAGATTTTTCCTTCCAGGAAATTGAGAAAGATATTCATAACTTTGAGTTTCAGTGGCAAGAAGATGAAAGAAATGGCCATGAAGCACCCATGACAAAAATCAAAAAATTGATGGGTAGTACAGAGCAATATGATCACAGGCATGCTGGAAACAAGCCTATTAAATATCAGCTTGGATCAAGCTTTCATTCACATCTGTCTGAACTCCACATATTTCAGCCCAAAGGGAAAATTAATAATCAAGTGGAGAAGTCTATCAACGATGCTTCCTCGGTTTCAACAGCCCAAAGAATTTCTTGTAGGCCCAAAACCCATATATCTAATAACTATGGGGATAATTTTCTGAATTATTCATTACTCACACAAAGACAGGAAGTACGCATGAGAGAAAAATCT

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000203326-'8-12,'8-4,11-12

Average complexity

C1

Mappability confidence:

100%=83=91%

Protein Impact

ORF disruption upon sequence exclusion

No structure available

Features

Disorder rate (Iupred):

C1=NA A=0.000 C2=0.147

Domain overlap (PFAM):

C1:

NA

A:

PF0135222=KRAB=WD(100=95.3)

C2:

PF0135222=KRAB=PD(0.1=0.0),PF134651=zf-H2C2_2=WD(100=6.0),PF134651=zf-H2C2_2=WD(100=6.0),PF134651=zf-H2C2_2=WD(100=6.0),PF134651=zf-H2C2_2=WD(100=6.0),PF134651=zf-H2C2_2=WD(100=5.8),PF134651=zf-H2C2_2=WD(100=6.0),PF134651=zf-H2C2_2=WD(100=5.8),PF134651=zf-H2C2_2=WD(100=6.0),PF134651=zf-H2C2_2=WD(100=5.8)

Main Inclusion Isoform:

ENSP00000419136