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Gene profile

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
PhenotypeIdentifierArticlesMentions
Turner syndrome11

Linked variants

Variants normalized to SDS
VariantHGVS / rsIDArticlesMentions

No normalized variants are linked to this gene.

Population context

Reported in the same publications
Country / regionGroupCohortArticles
Saudi Arabia1
Not specified1
Not specified2521
Not specified5,4951

Supporting publications

9 records
  1. 2024Exploring genetic diversity and variation of Ovar-DRB1 gene in Sudan Desert Sheep using targeted next-generation sequencing.BMC genomicsPubMed ↗
  2. 2024Palm kernel meal regulates the expression of genes involved in the amino acid metabolism in the liver of Tibetan sheep.BMC veterinary researchPubMed ↗
  3. 2023Genetic variation and demographic history of Sudan desert sheep reveal two diversified lineages.BMC genomicsPubMed ↗
  4. 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 ↗
  5. 2022Biallelic POC1A variants cause syndromic severe insulin resistance with muscle cramps.European journal of endocrinologyPubMed ↗
  6. 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 ↗
  7. 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 ↗
  8. 2016A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.Clinical geneticsPubMed ↗
  9. 2016Partial Loss of Function of the GHRH Receptor Leads to Mild Growth Hormone Deficiency.The Journal of clinical endocrinology and metabolismPubMed ↗