Special

HsaEX0040401 @ hg38

Exon Skipping

Gene
Description
metastasis associated 1 family member 3 [Source:HGNC Symbol;Acc:HGNC:23784]
Coordinates
chr2:42659763-42695839:+
Coord C1 exon
chr2:42659763-42659862
Coord A exon
chr2:42682401-42682589
Coord C2 exon
chr2:42695765-42695839
Length
189 bp
Sequences
Splice sites
3' ss Seq
TGTTCATTTTGTTTCTTTAGTTT
3' ss Score
8.88
5' ss Seq
TTTGTAAGT
5' ss Score
7.4
Exon sequences
Seq C1 exon
TGCTGTTGGGACATTCGCCAGAGCCCTGGATTGCAGCAGTTCTGTGAGGCAGCCTAGTTTGCATATGAGTGCTGCTGCAGCTTCCCGAGACATCACCTTG
Seq A exon
TTTCACGCTATGGATACATTGTATAGACACAGCTATGATTTGAGCAGTGCCATTAGTGTCTTAGTACCACTCGGAGGACCTGTTTTATGCAGAGATGAAATGGAGGAATGGTCAGCCTCTGAAGCTAGCTTATTTGAAGAGGCACTGGAAAAATATGGCAAAGACTTCAATGACATACGGCAAGATTTT
Seq C2 exon
CTTCCTTGGAAATCATTGACTAGCATCATTGAATATTATTACATGTGGAAAACTACTGACAGATATGTGCAACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000057935_MULTIEX1-3/10=2-5
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (disopred):
  C1=0.489 A=0.050 C2=0.149
Domain overlap (PFAM):

C1:
PF0144819=ELM2=PD(5.5=8.8)
A:
PF0024926=Myb_DNA-binding=PU(61.7=46.0)
C2:
PF0024926=Myb_DNA-binding=PD(34.0=64.0)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CTGTTGGGACATTCGCCAGAG
R:
TGTTGCACATATCTGTCAGTAGT
Band lengths:
172-361
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development