HsaEX0074286 @ hg19

Exon Skipping

Gene

ENSG00000185252 | ZNF74

Description

zinc finger protein 74 [Source:HGNC Symbol;Acc:13144]

Coordinates

chr22:20749623-20761968:+

Coord C1 exon

chr22:20749623-20749708

Coord A exon

chr22:20754922-20755048

Coord C2 exon

chr22:20759667-20761968

Length

127 bp

Sequences

Splice sites

3' ss Seq

GAACCTATATGTCATTTCAGGAA

3' ss Score

6.14

5' ss Seq

TAGGTAAAA

5' ss Score

6.02

Exon sequences

Seq C1 exon

CTCTTTCCTCTCAGGATCCTGCTCTTTCCCTGAAAGAGAATCTCGAGGATATATCGGGTTGGGGTCTTCCCGAAGCCAGGTCCAAG

Seq A exon

GAATCGGTGAGTTTCAAGGATGTGGCTGTGGACTTCACCCAGGAGGAGTGGGGTCAACTAGACTCCCCTCAGAGGGCCTTGTACCGGGATGTGATGTTGGAGAACTACCAGAACCTTCTTGCCCTAG

Seq C2 exon

AATGGGAGCTGAAGGCGGTGCCCTCTCAACAGCAGGGCATTTGCAAAGAAGAACCGGCCCAGGAGCCCATCATGGAGCGGCCCCTCGGCGGGGCGCAGGCGTGGGGGCGCCAGGCAGGTGCTCTGCAGAGGAGTCAGGCTGCGCCCTGGGCGCCCGCACCTGCCATGGTCTGGGACGTCCCTGTAGAGGAATTCCCCCTCAGGTGTCCCCTCTTCGCCCAGCAACGCGTTCCCGAGGGGGGACCCTTGCTGGACACACGCAAGAACGTCCAGGCCACTGAGGGCAGAACCAAGGCCCCCGCGAGACTGTGTGCAGGGGAAAACGCCTCCACGCCAAGTGAGCCAGAAAAGTTCCCCCAGGTGCGCCGGCAGCGCGGGGCGGGCGCCGGGGAGGGCGAGTTCGTGTGCGGCGAGTGCGGGAAGGCGTTCCGCCAGAGCTCCTCCCTCACGCTGCACCGGCGCTGGCACAGCCGGGAGAAGGCTTACAAGTGCGATGAATGC

VastDB Features

Vast-tools module Information

Secondary ID

ENSG00000185252_MULTIEX1-4/6=2-6

Average complexity

C3

Mappability confidence:

100%=100=100%

Protein Impact

ORF disruption upon sequence exclusion

No structure available

Features

Disorder rate (Iupred):

C1=0.436 A=0.345 C2=0.264

Domain overlap (PFAM):

C1:

NO

A:

PF0135222=KRAB=WD(100=95.3)

C2:

PF0135222=KRAB=PD(0.1=0.0),PF127602=Zn_Tnp_IS1595=WD(100=8.5),PF134651=zf-H2C2_2=WD(100=4.7),PF054957=zf-CHY=WD(100=15.6),PF134651=zf-H2C2_2=WD(100=4.9),PF134081=Zn_ribbon_recom=WD(100=9.6),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=4.9),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.9),PF134651=zf-H2C2_2=WD(100=4.9),PF0009621=zf-C2H2=WD(100=4.3)

Main Inclusion Isoform:

ENSP00000385855