HsaEX0073287 @ hg19

Exon Skipping

Gene

ENSG00000174652 | ZNF266

Description

zinc finger protein 266 [Source:HGNC Symbol;Acc:13059]

Coordinates

chr19:9523272-9528584:-

Coord C1 exon

chr19:9528504-9528584

Coord A exon

chr19:9526330-9526418

Coord C2 exon

chr19:9523272-9525396

Length

89 bp

Sequences

Splice sites

3' ss Seq

ACATTTCTTTTTCTCTTCAGCTT

3' ss Score

9.74

5' ss Seq

ATGGTAAGA

5' ss Score

9.48

Exon sequences

Seq C1 exon

GATATCAGCTCTTCAAACCCAGTCTGATCTCTTGGCTGGAACAAGAAGAGTCTAGGACAGTGCAGAGAGGTGATTTCCAAG

Seq A exon

CTTCAGAATGGAAAGTGCAACTTAAAACCAAAGAGTTAGCCCTTCAGCAGGATGTTTTGGGGGAGCCAACCTCCAGTGGGATTCAAATG

Seq C2 exon

ATAGGAAGCCACAACGGAGGGGAGGTCAGTGATGTTAAGCAATGTGGAGATGTCTCCAGTGAACACTCATGCCTTAAGACACATGTGAGAACTCAAAATAGTGAGAACACATTTGAGTGTTATCTGTATGGAGTAGACTTCCTTACTCTGCACAAGAAAACCTCTACTGGAGAGCAACGTTCTGTATTTAGTCAGTGTGGAAAAGCCTTCAGCCTGAACCCAGATGTTGTTTGCCAGAGAACGTGCACAGGAGAGAAAGCTTTTGATTGCAGTGACTCTGGGAAATCCTTCATTAATCATTCACACCTTCAGGGACATTTAAGAACTCACAATGGAGAAAGTCTCCATGAATGGAAGGAATGTGGGAGAGGCTTTATTCACTCCACAGACCTTGCTGTGCGTATACAAACTCACAGGTCAGAAAAACCCTACAAATGTAAGGAATGTGGAAAAGGATTTAGATATTCTGCATACCTTAATATTCACATGGGAACCCACAC

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000174652_CASSETTE1

Average complexity

S

Mappability confidence:

100%=100=100%

Protein Impact

ORF disruption upon sequence exclusion

Show structural model

Features

Disorder rate (Iupred):

C1=0.000 A=0.133 C2=0.065

Domain overlap (PFAM):

C1:

NO

A:

NO

C2:

PF134651=zf-H2C2_2=WD(100=5.4),PF134651=zf-H2C2_2=WD(100=4.4),PF0013017=C1_1=WD(100=12.2),PF134651=zf-H2C2_2=WD(100=5.4),PF134651=zf-H2C2_2=WD(100=5.4),PF134651=zf-H2C2_2=WD(100=5.2),PF134651=zf-H2C2_2=WD(100=5.4),PF134651=zf-H2C2_2=WD(100=5.2),PF134651=zf-H2C2_2=WD(100=5.4),PF134651=zf-H2C2_2=WD(100=5.2),PF134651=zf-H2C2_2=WD(100=5.4),PF134651=zf-H2C2_2=WD(100=5.2),PF134651=zf-H2C2_2=WD(100=5.2),PF0013017=C1_1=WD(100=10.6),PF134651=zf-H2C2_2=WD(100=5.4)

Main Inclusion Isoform:

ENSP00000354680