Gene

KMT2D

HGNC: HGNC:7133 | GeneCards: KMT2D
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 KMT2D. Co-mention, not a proven association.

PhenotypeArticlesEvidence
developmental delay3View sentences
COVID-191View sentences
breast cancer1View sentences
coronary artery disease1View sentences
epilepsy1View sentences
hypertension1View sentences
intellectual disability1View sentences
neurodevelopmental disorder1View sentences

Reported variants

Variants linked to KMT2D 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 KMT2D.

No Saudi region named.