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HBFQTL4 Fetal hemoglobin QTL on chromosome 8 [ Homo sapiens (human) ]

Gene ID: 171515, updated on 16-Aug-2019

Summary

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Gene symbol
HBFQTL4
Gene description
Fetal hemoglobin QTL on chromosome 8
Primary source
MIM:606789
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FHQTL

Genomic context

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Location:
8q

Bibliography

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Related articles in PubMed

  1. The XmnI and BCL11A single nucleotide polymorphisms may help predict hydroxyurea response in Iranian β-thalassemia patients. Banan M, et al. Hemoglobin, 2012. PMID 22686296
  2. Characterization of myelodysplastic syndrome and aplastic anemia by immunostaining of p53 and hemoglobin F and karyotype analysis: differential diagnosis between refractory anemia and aplastic anemia. Iwasaki T, et al. Pathol Int, 2008 Jun. PMID 18477214

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Data indicate that single nucleotide polymorphisms (SNPs) in three Hb F quantitative trait loci (QTLs) may be used to accurately predict the hydroxyurea (HU) response of Iranian beta-thalassemia (beta-thal) patients.
    Title: The XmnI and BCL11A single nucleotide polymorphisms may help predict hydroxyurea response in Iranian β-thalassemia patients.
  2. The data show that immunostaining for p53 and HbF as well as karyotype analysis are useful for the differential diagnosis of myelodysplastic syndrome and aplastic anemia.
    Title: Characterization of myelodysplastic syndrome and aplastic anemia by immunostaining of p53 and hemoglobin F and karyotype analysis: differential diagnosis between refractory anemia and aplastic anemia.
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Phenotypes

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Fetal hemoglobin QTL on chromosome 8

General gene information

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Markers

Property

  • phenotype only

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