HsaEX6062025 @ hg38

Exon Skipping

Gene

ENSG00000196597 | ZNF782

Description

zinc finger protein 782 [Source:HGNC Symbol;Acc:HGNC:33110]

Coordinates

chr9:96816472-96845016:-

Coord C1 exon

chr9:96844890-96845016

Coord A exon

chr9:96827080-96827181

Coord C2 exon

chr9:96816472-96819778

Length

102 bp

Sequences

Splice sites

3' ss Seq

AAATTGTTTCCCATTTATAGGCT

3' ss Score

7.89

5' ss Seq

CAGGTGAGT

5' ss Score

10.67

Exon sequences

Seq C1 exon

GCATCAGTGTCATTCCAGGACGTGACTGTGGAATTCAGCCAGGAGGAGTGGCAGCACATGGGCCCTGTTGAGAGGACCCTGTACAGAGATGTGATGCTGGAGAACTACAGCCACCTCGTCTCAGTGG

Seq A exon

GCTACTGCTTTACAAAACCAGAACTGATCTTCACATTGGAACAAGGAGAAGATCCATGGTTATTAGAGAAAGAGAAAGGATTTCTAAGCAGGAACTCCCCAG

Seq C2 exon

AAGACTCCCAACCTGATGAAATCTCAGAGAAGAGCCCAGAAAATCAAGGCAAACATTTGTTGCAAGTTTTATTCACCAATAAATTATTGACTACAGAGCAAGAAATTTCAGGAAAACCACATAATCGAGACATAAACATTTTTCGTGCAAGAATGATGCCTTGTAAATGTGACATTGCGGGGTCTGCTTGCCAGGGGCTCAGCCTGATGGCCCCACACTGTCAGTATTCAAAAGAAAAGGCTCATGAGCGTAATGTTTGTGACAAATGGCTCATCAGTATTAAGGATGGCAGAACTAACACTCAAGAGAAATCTTTCGCTTATAGTAAAATTGTGAAAACCCTCCATCATAAGGAGGAAGTTATTCAACATCAGACAATTCAGACTCTGGGGCAAGATTTTGAATATAATGAAAGTAGAAAAGCTTTTCTTGAAAAGGCTGCCCTTGTTACATCTAACAGTACCCACCCAAAAGGAAAATCTTACAATTTCAATAAATTT

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000196597-'12-26,'12-21,14-26

Average complexity

C1

Mappability confidence:

100%=100=100%

Protein Impact

Alternative protein isoforms (Ref)

No structure available

Features

Disorder rate (Iupred):

C1=0.000 A=0.136 C2=0.221

Domain overlap (PFAM):

C1:

PF0135222=KRAB=WD(100=95.3)

A:

PF0135222=KRAB=PD(0.1=0.0)

C2:

PF134651=zf-H2C2_2=WD(100=4.8),PF134651=zf-H2C2_2=WD(100=4.2),PF134651=zf-H2C2_2=WD(100=4.2),PF134651=zf-H2C2_2=WD(100=4.0),PF134651=zf-H2C2_2=WD(100=4.0),PF134651=zf-H2C2_2=WD(100=4.2),PF134651=zf-H2C2_2=WD(100=4.2),PF0013017=C1_1=WD(100=8.2),PF134651=zf-H2C2_2=WD(100=4.2),PF134651=zf-H2C2_2=WD(100=4.2),PF134651=zf-H2C2_2=WD(100=4.2),PF134651=zf-H2C2_2=WD(100=4.2)

Main Inclusion Isoform:

ENSP00000419397