HsaEX0074331 @ hg19

Exon Skipping

Gene

ENSG00000152439 | ZNF773

Description

zinc finger protein 773 [Source:HGNC Symbol;Acc:30487]

Coordinates

chr19:58016670-58024436:+

Coord C1 exon

chr19:58016670-58016768

Coord A exon

chr19:58017726-58017961

Coord C2 exon

chr19:58024390-58024436

Length

236 bp

Sequences

Splice sites

3' ss Seq

CAACATTTCTCTTCTTTCAGGTA

3' ss Score

10.6

5' ss Seq

CAGGTGACT

5' ss Score

6.6

Exon sequences

Seq C1 exon

GACTTGCATCTTCCAAGACCCATGAAATAACCCAGCTGGAGTCATGGGAGGAGCCCTTCATGCCTGCTTGGGAAGTTGTGACTTCAGCCATACTGAGAG

Seq A exon

GTAGTTGGCAAGGAGCCAAGGCTGAGGCAGCTGCTGAGCAGAGTGCTTCTGTAGAAGTGCCCAGTTCAAACGTTCAGCAACACCAGAAGCAGCACTGTGGAGAGAAACCCTTAAAAAGACAAGAGGGCAGGGTCCCAGTTTTGAGGAGTTGCAGAGTCCACCTATCAGAGAAGTCCTTGCAAAGCAGGGAAGTTGGGAAGGATCTTCTGACCAGCTCAGGTGTTCTCAAGCACCAG

Seq C2 exon

TCCCGAACCGACAGCCACAAGTGGCGCCCGAACAGGGACGTGAGTGA

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000152439_MULTIEX2-1/2=C1-C2

Average complexity

ME(1-2[94=100])

Mappability confidence:

100%=100=100%

Protein Impact

ORF disruption upon sequence inclusion

No structure available

Features

Disorder rate (Iupred):

C1=0.000 A=0.203 C2=0.700

Domain overlap (PFAM):

C1:

PF0135222=KRAB=PD(0.1=0.0)

A:

PF134651=zf-H2C2_2=WD(100=7.3),PF134651=zf-H2C2_2=WD(100=7.3),PF0013017=C1_1=WD(100=14.6),PF134651=zf-H2C2_2=WD(100=7.3),PF134651=zf-H2C2_2=WD(100=7.0),PF0013017=C1_1=WD(100=14.9),PF134651=zf-H2C2_2=WD(100=7.3),PF134651=zf-H2C2_2=WD(100=7.3),PF0013017=C1_1=WD(100=14.0),PF134651=zf-H2C2_2=WD(100=7.3),PF134651=zf-H2C2_2=WD(100=7.3)

C2:

NO

Main Inclusion Isoform:

ENSP00000282292