Gene

SAMHD1

HGNC: HGNC:15925 | GeneCards: SAMHD1
Saudi human-genetics coreAll Saudi-affiliated records

Overview

Approved name
Cytogenetic location
-
Locus type
-
In SaudiVarKB
8 articles, 8 mentions

Synonyms

None recorded

External resources

ClinVar ↗PubMed ↗
8Publications8Co-reported phenotypes
0Reported variants
0ClinVar pathogenic / likely pathogenic
0Saudi regions
OpenLiterature network

Co-reported phenotypes

Phenotypes named in the same articles as SAMHD1. Co-mention, not a proven association.

PhenotypeArticlesEvidence
HIV infection2View sentences
leukemia2View sentences
COVID-191View sentences
developmental delay1View sentences
epilepsy1View sentences
intellectual disability1View sentences
neurodevelopmental disorder1View sentences
stroke1View sentences

Reported variants

Variants linked to SAMHD1 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 SAMHD1.

No Saudi region named.