Gene

HOXA1

HGNC: HGNC:5099 | GeneCards: HOXA1
Saudi human-genetics coreAll Saudi-affiliated records

Overview

Approved name
Cytogenetic location
-
Locus type
-
In SaudiVarKB
16 articles, 16 mentions

Synonyms

None recorded

External resources

ClinVar ↗PubMed ↗
16Publications9Co-reported phenotypes
0Reported variants
0ClinVar pathogenic / likely pathogenic
0Saudi regions
OpenLiterature network

Co-reported phenotypes

Phenotypes named in the same articles as HOXA1. Co-mention, not a proven association.

PhenotypeArticlesEvidence
hearing loss6View sentences
intellectual disability4View sentences
autism spectrum disorder2View sentences
congenital heart disease2View sentences
arthrogryposis1View sentences
cleft lip and palate1View sentences
developmental delay1View sentences
diabetes mellitus1View sentences
epilepsy1View sentences

Reported variants

Variants linked to HOXA1 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 HOXA1.

No Saudi region named.