SDS
HGNC:10691 · SaudiVarKB evidence summary derived from retained literature mentions.
9Gene mentions
9Publications
0Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in SDS publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| Turner syndrome | — | 1 | 1 |
Linked variants
Variants normalized to SDS| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | — | 1 |
| Not specified | — | — | 1 |
| Not specified | — | 252 | 1 |
| Not specified | — | 5,495 | 1 |
Supporting publications
9 records- 2024Exploring genetic diversity and variation of Ovar-DRB1 gene in Sudan Desert Sheep using targeted next-generation sequencing.BMC genomicsPubMed ↗
- 2024Palm kernel meal regulates the expression of genes involved in the amino acid metabolism in the liver of Tibetan sheep.BMC veterinary researchPubMed ↗
- 2023Genetic variation and demographic history of Sudan desert sheep reveal two diversified lineages.BMC genomicsPubMed ↗
- 2023Association of High and Low Molecular Weight Glutenin Subunits with Gluten Strength in Tetraploid Durum Wheat (Triticum turgidum spp. Durum L.).Plants (Basel, Switzerland)PubMed ↗
- 2022Biallelic POC1A variants cause syndromic severe insulin resistance with muscle cramps.European journal of endocrinologyPubMed ↗
- 2020Effect of growth hormone treatment on children with idiopathic short stature (ISS), idiopathic growth hormone deficiency (IGHD), small for gestational age (SGA) and Turner syndrome (TS) in a tertiary care center.Acta bio-medica : Atenei ParmensisPubMed ↗
- 2017Combination of real-time PCR and sequencing to detect multiple clinically relevant genetic variations in the lactase gene.Scandinavian journal of clinical and laboratory investigationPubMed ↗
- 2016A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.Clinical geneticsPubMed ↗
- 2016Partial Loss of Function of the GHRH Receptor Leads to Mild Growth Hormone Deficiency.The Journal of clinical endocrinology and metabolismPubMed ↗