HsaEX0073949 @ hg38

Exon Skipping

Gene

ENSG00000186017 | ZNF566

Description

zinc finger protein 566 [Source:HGNC Symbol;Acc:HGNC:25919]

Coordinates

chr19:36447629-36476616:-

Coord C1 exon

chr19:36476549-36476616

Coord A exon

chr19:36473332-36473458

Coord C2 exon

chr19:36447629-36450001

Length

127 bp

Sequences

Splice sites

3' ss Seq

ATACGTGGTTATTGTTCCAGGAG

3' ss Score

6.76

5' ss Seq

TGGGTAAGG

5' ss Score

9.08

Exon sequences

Seq C1 exon

CTCTACCCTTCTCCAAAAGAAGAGCCAAGAGAAGGTCCTTTTCTACAAATATCAGAGCCATGGCTCAG

Seq A exon

GAGTCAGTGATGTTCAGTGATGTGTCCGTAGACTTCTCTCAGGAGGAGTGGGAATGCCTGAATGATGATCAGAGAGATTTATACAGAGATGTGATGTTGGAGAATTACAGCAACCTGGTTTCAATGG

Seq C2 exon

TCCTGGAATCAAGATGTGAGACCAAGAAATTATTTCTGAAGAAAGAAATTTATGAAATAGAATCAACCCAGTGGGAAATAATGGAAAAACTCACAAGACGTGATTTTCAGTGCTCCAGTTTCAGAGATGATTGGGAATGTAATCGGCAGTTTAAGAAAGAACTCGGCTCTCAGGGGGGACATTTCAATCAATTGGTATTCACTCATGAAGATCTGCCCACTTTGAGTCACCATCCATCCTTCACATTACAGCAAATCATTAACAGTAAAAAGAAATTCTGTGCATCTAAAGAATATAGGAAAACCTTTAGACATGGCTCACAGTTTGCTACACATGAGATAATTCATACCATTGAGAAGCCTTATGAATGTAAGGAATGTGGAAAGTCCTTTAGACATCCCTCAAGACTCACTCATCATCAGAAAATTCATACTGGCAAGAAACCCTTTGAATGTAAGGAATGTGGAAAAACCTTTATTTGTGGCTCAGACCTTACTCGA

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000186017_MULTIEX1-2/5=1-4

Average complexity

C2

Mappability confidence:

100%=100=100%

Protein Impact

ORF disruption upon sequence exclusion

Show structural model

Features

Disorder rate (Iupred):

C1=0.000 A=0.000 C2=0.068

Domain overlap (PFAM):

C1:

NO

A:

PF0135222=KRAB=WD(100=95.3)

C2:

PF134651=zf-H2C2_2=WD(100=7.3),PF134651=zf-H2C2_2=WD(100=7.6),PF134651=zf-H2C2_2=WD(100=7.6),PF097235=Zn-ribbon_8=WD(100=12.0),PF134651=zf-H2C2_2=WD(100=7.6),PF134651=zf-H2C2_2=WD(100=7.6),PF134651=zf-H2C2_2=WD(100=7.6),PF134651=zf-H2C2_2=WD(100=7.6),PF134651=zf-H2C2_2=WD(100=7.6)

Main Inclusion Isoform:

ENSP00000376010