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ACKR1 and thalassemia are reported together in 1 article.
Gene
ACKR1
- HGNC
- HGNC:4035
1articles
1mentions
1variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype
Thalassemia
- HPO
- HP:0001878
409articles
409mentions
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 60Idiopathic Thrombocytosis in Alpha Thalassemia Trait Patient.
PMID 38514054 · Annals of clinical and laboratory science · 2024 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ACKR1 | “Noticeably, a variant in atypical chemokine receptor 1 (ACKR1) (c.-67T>C, rs2814778) was found to be homozygous.” | 0.98 | hgnc_dict_v1 |
| phenotype | thalassemia | “Idiopathic Thrombocytosis in Alpha Thalassemia Trait Patient.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | leukemia | “The patient was positive for alpha thalassemia trait; negative for mutation in Janus kinase 2, calreticulin, or myeloproliferative leukemia virus oncogene; and negative for reactive causes of thrombocytosis.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | c.-67T>C | “Noticeably, a variant in atypical chemokine receptor 1 (ACKR1) (c.-67T>C, rs2814778) was found to be homozygous.” | 0.95 | hgvs_regex_v1 |