HsaEX0073618 @ hg19

Exon Skipping

Gene

ENSG00000083817 | ZNF416

Description

zinc finger protein 416 [Source:HGNC Symbol;Acc:20645]

Coordinates

chr19:58082934-58089466:-

Coord C1 exon

chr19:58089425-58089466

Coord A exon

chr19:58087172-58087298

Coord C2 exon

chr19:58082934-58085069

Length

127 bp

Sequences

Splice sites

3' ss Seq

ATCTATCCCCATCATGGCAGGGC

3' ss Score

5.81

5' ss Seq

TGGGTAAGG

5' ss Score

9.08

Exon sequences

Seq C1 exon

GTTCCCGTGACTGCAGAAGCTAAACTTATGGGCTTTACACAG

Seq A exon

GGCTGTGTGACCTTTGAGGACGTGGCCATTTACTTCTCCCAGGAAGAATGGGGGCTCCTTGATGAGGCTCAGAGGCTCCTGTACCGCGATGTGATGCTGGAGAACTTTGCACTTATAACTGCGCTGG

Seq C2 exon

TTTGTTGGCATGGGATGGAGGATGAAGAGACACCTGAGCAAAGTGTTTCTGTAGAAGGAGTACCTCAGGTCAGGACTCCAGAGGCCAGTCCATCCACCCAGAAGATTCAATCCTGTGACATGTGTGTCCCATTCCTGACCGACATTTTGCACCTGACCGATTTGCCTGGGCAGGAACTATACTTGACTGGGGCATGTGCGGTCTTTCACCAGGACCAGAAGCATCATAGTGCAGAGAAACCCTTGGAAAGTGACATGGACAAGGCCTCATTTGTGCAGTGCTGCCTGTTCCATGAGTCAGGAATGCCTTTCACCAGCAGTGAGGTTGGGAAGGACTTCCTAGCCCCATTGGGCATTCTTCAGCCGCAAGCTATTGCTAACTATGAGAAGCCAAACAAAATCAGCAAATGTGAGGAGGCCTTTCATGTTGGAATAAGTCATTACAAGTGGAGTCAATGCAGGAGAGAGTCCAGCCACAAACACACTTTTTTTCACCCTAGA

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000083817-'2-3,'2-2,3-3

Average complexity

S

Mappability confidence:

100%=100=100%

Protein Impact

ORF disruption upon sequence exclusion

No structure available

Features

Disorder rate (Iupred):

C1=0.000 A=0.000 C2=0.115

Domain overlap (PFAM):

C1:

NO

A:

PF0135222=KRAB=WD(100=95.3)

C2:

PF0135222=KRAB=PD(0.1=0.0),PF134651=zf-H2C2_2=WD(100=4.0),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.5),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.9)

Main Inclusion Isoform:

ENSP00000196489