HsaEX0072998 @ hg38

Exon Skipping

Gene

ENSG00000181896 | ZNF101

Description

zinc finger protein 101 [Source:HGNC Symbol;Acc:HGNC:12881]

Coordinates

chr19:19677864-19680554:+

Coord C1 exon

chr19:19677864-19677990

Coord A exon

chr19:19678726-19678786

Coord C2 exon

chr19:19679181-19680554

Length

61 bp

Sequences

Splice sites

3' ss Seq

TCTCTGGGTCTACATTTTAGGAA

3' ss Score

8.06

5' ss Seq

AAGGTAATC

5' ss Score

7.46

Exon sequences

Seq C1 exon

GACTCAGTGGCCTTTGAGGATGTGGCTGTGAACTTCACCCAGGAGGAGTGGGCTTTGCTGAGTCCTTCCCAGAAGAATCTCTACAGAGATGTGACGCTGGAAACCTTCAGGAACCTGGCCTCGGTCG

Seq A exon

GAATCCAATGGAAAGACCAGGACATTGAGAATCTGTACCAAAACCTGGGGATTAAGCTAAG

Seq C2 exon

AAGTCTGGTGGAGAGACTCTGTGGACGTAAAGAAGGGAATGAACACAGAGAAACTTTCAGCCAGATTCCTGATTGTCACCTGAACAAGAAAAGTCAAACTGGAGTGAAACCATGCAAATGCAGCGTGTGTGGGAAAGTCTTCCTCCGTCATTCATTCCTGGACAGGCACATGAGAGCTCATGCTGGACACAAACGATCTGAGTGTGGTGGGGAATGGAGAGAGACGCCCCGTAAACAGAAACAACATGGGAAAGCCTCCATTTCCCCCAGTAGTGGTGCACGGCGCACAGTAACACCAACTCGAAAGAGACCTTATGAATGCAAGGTGTGCGGGAAAGCCTTTAATTCTCCCAATTTATTTCAAATCCATCAAAGAACTCACACTGGAAAGAGGTCCTATAAATGTAGGGAAATAGTGAGAGCCTTCACAGTTTCCAGTTTCTTTCGAAAACATGGAAAAATGCATACTGGAGAAAAACGCTATGAATGTAAATACTGTG

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000181896_MULTIEX1-1/2=C1-2

Average complexity

S

Mappability confidence:

100%=100=100%

Protein Impact

Alternative protein isoforms (Ref, Alt. Stop)

No structure available

Features

Disorder rate (Iupred):

C1=0.000 A=0.000 C2=0.126

Domain overlap (PFAM):

C1:

PF0135222=KRAB=PU(95.0=92.7)

A:

PF0135222=KRAB=PD(0.1=0.0)

C2:

PF0009621=zf-C2H2=WD(100=6.1),PF0009621=zf-C2H2=WD(100=6.1),PF134651=zf-H2C2_2=WD(100=5.9),PF134651=zf-H2C2_2=WD(100=7.0),PF134651=zf-H2C2_2=WD(100=7.0),PF134651=zf-H2C2_2=WD(100=7.0),PF134651=zf-H2C2_2=WD(100=6.4),PF134651=zf-H2C2_2=WD(100=6.7)

Main Inclusion Isoform:

ENSP00000319716