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Date: Fri Dec 13 2024
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SLC25A25-AS1
Homo sapiens
HGNC:27844
Summary
Orthology
Paralogy
Function - GO Annotations
Pathways
Phenotypes
Disease Associations
Alleles and Variants
Transgenic Alleles
Models
Sequence Feature Viewer
Sequence Details
Expression
Molecular Interactions
Genetic Interactions
Gene
SLC25A25-AS1
Species
Homo sapiens
Symbol
SLC25A25-AS1
Name
SLC25A25 antisense RNA 1
Synonyms
HRCEG
Biotype
ncRNA gene
Automated Description
Not Available
RGD Description
ASSOCIATED WITH congenital disorder of glycosylation Iu; developmental and epileptic encephalopathy; early infantile epileptic encephalopathy; INTERACTS WITH aristolochic acid A; cisplatin; dicrotophos
Cross References
ENSEMBL:ENSG00000234771
NCBI_Gene:100289019
Show All 3
Additional Information
Literature
Orthology
Gene tree
Not Available
Links to orthology data in JBrowse by filter level:
Stringent
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Moderate
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No filter
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Best and Best Reverse
Paralogy
Function - GO Annotations
Show functions with at least one experimental evidence
Pathways
Reactome Pathway (0)
Reactome Reactions (0)
GO-CAMs (0)
No data available
No data available
No data available
Read more about the
GO-CAM Data Model
.
Phenotypes
Primary Sources
None
Other Sources
BioGRID CRISPR Screen Cell Line Phenotypes
Disease Associations
Include negative annotations
Cases where the expected disease association was NOT found
Cell color indicative of annotation volume
Alleles and Variants
Download all Alleles/Variants for all genes of the species
Transgenic Alleles
Models
Sequence Feature Viewer
Genome location
Chr9:128108581...128118734
- (10.15 kb)
Assembly version
GRCh38
Viewer Help
128.109M
128.110M
128.111M
128.112M
128.113M
128.114M
128.115M
128.116M
128.117M
128.118M
Sequence Details
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Expression
Primary Sources
None
Other Sources
GEO
Single Cell Expression Atlas
Expression Atlas
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.
Molecular Interactions
Genetic Interactions
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