HsaEX6092687 @ hg38

Exon Skipping

Gene

ENSG00000130803 | ZNF317

Description

zinc finger protein 317 [Source:HGNC Symbol;Acc:HGNC:13507]

Coordinates

chr19:9157980-9163413:+

Coord C1 exon

chr19:9157980-9158075

Coord A exon

chr19:9158826-9158908

Coord C2 exon

chr19:9160114-9163413

Length

83 bp

Sequences

Splice sites

3' ss Seq

ACTTTTCCAATTTGTTTCAGATT

3' ss Score

10.36

5' ss Seq

ATGGTAAGA

5' ss Score

9.48

Exon sequences

Seq C1 exon

GGTATCAGGTCGGCAAACCCAGCCTCATCTCACACTTGGAGCAGGAGGAGGAGCCGAGGACAGAGGAGAGGGGCGCTCACCAGGGCGCTTGTGCAG

Seq A exon

ATTGGGAGACTCCATCTAAAACCAAGTGGTCACTTCTTATGGAAGATATTTTTGGGAAGGAAACGCCCAGTGGTGTGACGATG

Seq C2 exon

GAAAGAGCCGGTCTTGGAGAGAAGTCCACTGAATACGCTCACTTGTTCGAAGTCTTTGGCATGGACCCTCATCTCACTCAGCCAATGGGAAGGCACGCTGGCAAGAGGCCCTATCACCGCCGCGACTATGGGGTAGCGTTCAAGGGCAGGCCGCACCTCACTCAGCACATGAGCATGTACGACGGGAGAAAAATGCATGAATGTCATCAGTGCCAAAAAGCCTTCACCACGAGCGCGTCCCTCACACGGCACAGGAGAATCCACACCGGGGAGAAGCCTTACGAGTGCAGCGACTGCGGGAAAGCCTTCAACGACCCTTCAGCCCTTAGGAGCCACGCAAGAACTCACCTCAAAGAGAAGCCCTTTGACTGCAGTCAGTGTGGAAATGCATTCCGGACCCTCTCGGCCCTGAAAATCCACATGCGAGTTCACACTGGCGAGAGGCCTTACAAGTGTGATCAGTGCGGGAAGGCTTACGGCCGGAGCTGCCACCTCATCGC

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000130803-'11-11,'11-10,12-11

Average complexity

C1

Mappability confidence:

100%=100=100%

Protein Impact

ORF disruption upon sequence exclusion

No structure available

Features

Disorder rate (Iupred):

C1=0.703 A=0.131 C2=0.120

Domain overlap (PFAM):

C1:

PF0135222=KRAB=PD(0.1=0.0)

A:

PF0135222=KRAB=PD(0.1=0.0)

C2:

PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=5.7),PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=5.7),PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=5.7),PF134651=zf-H2C2_2=WD(100=5.9)

Main Inclusion Isoform:

ENSP00000247956