HsaEX0074046 @ hg38

Exon Skipping

Gene

ENSG00000142556 | ZNF614

Description

zinc finger protein 614 [Source:HGNC Symbol;Acc:HGNC:24722]

Coordinates

chr19:52013325-52018103:-

Coord C1 exon

chr19:52018008-52018103

Coord A exon

chr19:52017576-52017697

Coord C2 exon

chr19:52013325-52017359

Length

122 bp

Sequences

Splice sites

3' ss Seq

TTTTTTTTTTTTTTTTTTAGACT

3' ss Score

11.22

5' ss Seq

CAGGCATGT

5' ss Score

2.05

Exon sequences

Seq C1 exon

GGTATCAAACTAGCAAACCAGATGTACTCTCCAAGTTGGCACATGGACAAGAACCATGGACAACAGATGCTAAAATTCAGAATAAAAATTGTCCAG

Seq A exon

ACTGAGTCTCGCTCTATCACCCAGGCTGGAGTGCAATGGCCCAATCTCGGCTTGCTGCAACCTCGTCCTCCTGGGATCAAGTGATTCTCCTGCCTCAGCCTCCTGAATAGCTGGGATTACAG

Seq C2 exon

GAATCGGGAAAGTTGACAGTCATCTGCAAGAGCACTCTCCAAACCAAAGACTTCTGAAGAGCGTGCAGCAATGCAATGGACAGAATACACTTAGAAATATTGTACATCTCAGCAAGACACATTTTCCTATAGTGCAAAATCATGATACATTTGACTTGTACAGAAAAAATTTGAAATCAAGTTTAAGTTTAATCAACCAGAAGAGAAGACATGGAATAAATAACCCTGTTGAGTTTATTGGAGGTGAGAAAACACTTCTACATGGTAAGCATGAACGTACGCATACTAAAACTAGATTTTCTGAAAATGCAAAATGTATCCATACTAAATTCCAAGTCTTCAAGCATCAGAGGACTCAGAAAATTGAGAAACCCCATGCATGCATTGAATGTGAGCAAACCTTCCTTAGGAAGTCTCAGCTCATTTACCATGAGAACATTTGTATACAAGAGAATCCTGGAAGTGGTCAATGTGAGAAATTATCCAGAAGTGTCCTGTTC

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000142556_CASSETTE2

Average complexity

S

Mappability confidence:

100%=100=100%

Protein Impact

ORF disruption upon sequence inclusion

No structure available

Features

Disorder rate (Iupred):

C1=0.400 A=1.000 C2=0.134

Domain overlap (PFAM):

C1:

PF0135222=KRAB=PD(0.1=0.0)

A:

NO

C2:

PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=5.1),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=5.1),PF134651=zf-H2C2_2=WD(100=5.1),PF134651=zf-H2C2_2=WD(100=5.1),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=5.1),PF134651=zf-H2C2_2=WD(100=5.1)

Main Inclusion Isoform:

ENSP00000471869