HsaEX1044901 @ hg38

Exon Skipping

Gene

ENSG00000167380 | ZNF226

Description

zinc finger protein 226 [Source:HGNC Symbol;Acc:HGNC:13019]

Coordinates

chr19:44172860-44195899:+

Coord C1 exon

chr19:44172860-44172952

Coord A exon

chr19:44175498-44175661

Coord C2 exon

chr19:44195747-44195899

Length

164 bp

Sequences

Splice sites

3' ss Seq

TGAATCCTTTGTCCTTACAGGAG

3' ss Score

10.26

5' ss Seq

CAGGTAGGG

5' ss Score

9.46

Exon sequences

Seq C1 exon

GGCATCCACCCTTCAAACAAGATGTATCACCTATAGAAAGAAATGAGCAGCTTTGGATAATGACGACAGCAACCCGAAGACAGGGAAATTTAG

Seq A exon

GAGAGAAAAATCAAAGTAAGTTAATTACTGTTCAAGACAGAGAATCAGAAGAAGAGCTTTCTTGTTGGCAAATCTGGCAACAAATTGCAAATGACTTAACCAGGTGTCAAGACTCCATGATCAATAATTCTCAGTGTCACAAACAAGGTGATTTCCCTTACCAG

Seq C2 exon

GTATATGTGCATGAGAACCTTCTTTTCATCACCTTCCCTGGCTCCATTTGTCCTGCTACGGTGACACCAGTCTTTTAGTCCATACATTTGACTTCATGAGGAGTTTGCTATAATCAATTGAATGAAGAAGAAACATGTGGACCTGCTTTATAG

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000167380_MULTIEX1-10/14=8-14

Average complexity

C1

Mappability confidence:

99%=100=100%

Protein Impact

Alternative protein isoforms (Ref, Alt. Stop)

No structure available

Features

Disorder rate (Iupred):

C1=0.091 A=0.134 C2=NA

Domain overlap (PFAM):

C1:

PF0135222=KRAB=PD(0.1=0.0)

A:

PF134651=zf-H2C2_2=WD(100=3.3),PF134651=zf-H2C2_2=WD(100=3.0),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.4),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.4),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.6),PF134651=zf-H2C2_2=WD(100=3.4)

C2:

NA

Main Inclusion Isoform:

ENSP00000336719