Gene

SLC13A5

HGNC: HGNC:23089 | GeneCards: SLC13A5
Saudi human-genetics coreAll Saudi-affiliated records

Overview

Approved name
Cytogenetic location
-
Locus type
-
In SaudiVarKB
4 articles, 4 mentions

Synonyms

None recorded

External resources

ClinVar ↗PubMed ↗
4Publications4Co-reported phenotypes
0Reported variants
0ClinVar pathogenic / likely pathogenic
0Saudi regions
OpenLiterature network

Co-reported phenotypes

Phenotypes named in the same articles as SLC13A5. Co-mention, not a proven association.

PhenotypeArticlesEvidence
epilepsy4View sentences
developmental delay3View sentences
intellectual disability3View sentences
autism spectrum disorder1View sentences

Reported variants

Variants linked to SLC13A5 through dbSNP or LitVar2. ClinVar status is shown for core-subset variants.

No variants with a confirmed gene link.

Saudi regions

Regions or cities named in the abstracts of articles that mention SLC13A5.

No Saudi region named.