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Gene: SLC25A25-AS1 (SLC25A25 antisense RNA 1) Homo sapiens
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Symbol: SLC25A25-AS1
Name: SLC25A25 antisense RNA 1
Description: ASSOCIATED WITH congenital disorder of glycosylation Iu; early infantile epileptic encephalopathy; INTERACTS WITH cisplatin; dicrotophos; fipronil
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl9128,108,581 - 128,118,693 (-)Ensembl
GRCh389128,111,171 - 128,118,734 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh379130,873,450 - 130,881,013 (-)NCBIGRCh37GRCh37hg19GRCh37
Celera9101,525,374 - 101,532,937 (-)NCBI
Cytogenetic Map9q34.11NCBI
HuRef9100,488,116 - 100,495,674 (-)NCBIHuRef
CHM1_19131,025,492 - 131,033,048 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SLC25A25-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 8698677
Created: 2014-08-13
Species: Homo sapiens
Last Modified: 2019-12-25
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.