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ASIC5 and recurrent pregnancy loss are reported together in 1 article.

Gene

ASIC5

HGNC
HGNC:17537
1articles
1mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
36articles
36mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

1 records shown · first 60

Whole-Genome Sequencing Reveals Exonic Variation of ASIC5 Gene Results in Recurrent Pregnancy Loss.

PMID 34395479 | PMCID PMC8363113 | DOI 10.3389/fmed.2021.699672 · Frontiers in medicine · 2021 · 6 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneASIC5“Whole-Genome Sequencing Reveals Exonic Variation of ASIC5 Gene Results in Recurrent Pregnancy Loss.”0.98hgnc_dict_v1
phenotyperecurrent pregnancy loss“Whole-Genome Sequencing Reveals Exonic Variation of ASIC5 Gene Results in Recurrent Pregnancy Loss.”0.98phenotype_alias_lexicon_v2
populationSaudi Arabia“A family (dead fetus and parents) from Saudi Arabia with an earlier history of three unexplained RPLs at the ninth week of pregnancy was included in the study.”0.95saudi_context_rules_v1
variantc.680G>T“WGS of dead fetus identifies a novel homozygous exonic variation (NM_017419.3:c.680G>T) in ASIC5 (acid-sensing ion channel subunit family member 5) gene; the parents are heterozygous.”0.95hgvs_regex_v1