Special

HsaINT0152513 @ hg19

Intron Retention

Gene
ENSG00000157765 | SLC34A2
Description
solute carrier family 34 (sodium phosphate), member 2 [Source:HGNC Symbol;Acc:11020]
Coordinates
chr4:25665824-25667893:+
Coord C1 exon
chr4:25665824-25665952
Coord A exon
chr4:25665953-25667749
Coord C2 exon
chr4:25667750-25667893
Length
1797 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGA
5' ss Score
10.06
3' ss Seq
TGTTTGTTTGTTTTTCCCAGGAA
3' ss Score
9.86
Exon sequences
Seq C1 exon
AGAGAGACACCAAAGGGAAGATTCTCTGTTTCTTCCAAGGGATTGGGAGATTGATTTTACTTCTCGGATTTCTCTACTTTTTCGTGTGCTCCCTGGATATTCTTAGTAGCGCCTTCCAGCTGGTTGGAG
Seq A exon
GTAAGAATGAAAGGGTGAGAGGTCTGCGGGTGAGGGGCATTATCTTGAAATGTGGTTCCGAGAGTAAAACTCAGCAAGCCCTCTCCAGCTGCAGCCTCCTGGAGTGTTTTAGGACTGGAACCGACCTCAGATCATTTATGAAGTCTATGCTTTCCGTTATAGAAGAGAAAACTGAGGCCTATACAAAGGGCTATGACTTGGCCCAGGTGGCTTAGGCCAGGAGCTGGGGCTAGACTATTCCAAGCTATCCGCCAGTTGAGTTTGTCCACAAACCCCAGGCAGGAAGTTGTCTGACATACAGACTTAGCTGAGGAATTCCTATATCCTCCACACCAGAGAGAATTCTGGAATGAGAAAGAGTGCCCTTTCAAATATGGGCCCTTGCTGGGGGAAGGACAGGGCCCCTTCTCTGGGCTGGAGGAATCTGCATCCATTGTACTTACCTTCACAGCCCTTAGGGCTGCGTGTGCCCATGCAGTGTGAGAACCCAGGAGTGAAGTCACCATGTGCTTGGTTCCCTTTGTACCTCAATGGTGATGTCAGAAACAAACAAGCAGCACTCCGTCTACTGGGTGCAGGCATTTTCGGGGGCCCTCTATCAAACATTCTTTCCCAGAGCCCTCCCATTTACGGAGAGATCATGAACCAGCCCTGAGACTCACAGCCTGTGATTAGCAGAGTAAGATTCAGTCTCAGATCTGGGTGACACAAAGGACCATGGATTTCTGCAACCCTTGGTGCCTTTCTTGGGAACCCATCTGTGTGACTTGGGAGAGTTGGGGAGGTGGGCATTCATGGGAGAGCATGAGGGGCAAACACTTCCTGGACATTGCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCGGGCTGGAGTGCATTGGCGTGATCTCAGCTCACCGCGACCTCCACCTCCCGGCTTCAAGCGATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCGTGTTGGTCAGGCTGGTCTGCAACTACTGACCTCAGTTGTTCCGCCCGTCCTCCGCCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCTCCTGAACATTGCTTCTGGGCTCCCTGGTCCATGGGAGCATCAGCTAGGGGCTTTGCTGTCTGGTTATCTCAGACAAATCACCTGCATCCTCTGGGCTTCCACCTTCTTTATACAATGGACTTGGGAATGCATTGATGGTCTCAGGTACACTCTTGAGAATAACTCTCCCAGCATTCAATTACAGGCTGGTGCTAGGGCTAAGGGTGGATAGAGAGATCTACTCTTGGAGGATAAATCTGAATTGGGTATACACCCCAGAGACATCCAGGAGGCTCATTGGAACCCACTGGTCCCAGTATGGAGTTGAGGCTGGGTTCCTGAGCACAGAAGGGCTTGCTGACTGAGGAGTGTTTGAAGAGTGGGAGGATGCAGGGTGAAGGAACAAAAGTAACCAGGGGCTCACAGTGGGTCGGGAACCAGGGCAGAGAGACAGAGACAGGAGGCACGTGTGGGCAGCTAGTAGATTTCCTGCCTTATCGGGGCAGCACTGGGAAGAGGCATGGGGAAGCAAGATTCCTTGGGTGCCTGCAGCGATGGAGGCTGGACTCTGCAACCCACAGCCAGCTGGCCTTGGATGGAGACTTCTGTTTACTCAGTGCCCACCTAATCCCCCTCGATCACGTTGTGATTGTTTTTGTTTGTTTGTTTGTTTTTCCCAG
Seq C2 exon
GAAAAATGGCAGGACAGTTCTTCAGCAACAGCTCTATTATGTCCAACCCTTTGTTGGGGCTGGTGATCGGGGTGCTGGTGACCGTCTTGGTGCAGAGCTCCAGCACCTCAACGTCCATCGTTGTCAGCATGGTGTCCTCTTCAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000157765-SLC34A2:NM_001177998:4
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF077877=DUF1625=FE(59.7=100),PF0269010=Na_Pi_cotrans=PU(32.7=38.6)
A:
NA
C2:
PF077877=DUF1625=PD(37.5=77.1),PF0269010=Na_Pi_cotrans=FE(65.4=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGAGAGACACCAAAGGGAAGA
R:
GAAGAGGACACCATGCTGACA
Band lengths:
271-2068
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains