HBG2
Synonym(s): HBG-T1
Locus: 11p15.4
Protein: Gamma globin
Disorders
- Fetal Hemoglobin Quantitative Trait Locus 1
- Cyanosis, Transient Neonatal
- Hereditary Persistence of Fetal Hemoglobin
Tests
| Beta Globin (HBB) Deletion/Duplication method(s): ◦ Del/Dup (CNV) ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA |
| Hereditary Persistence of Fetal Hemoglobin (HPFH) 8 Mutations method(s): ◦ Genotyping (Microarray, Beads, etc.) ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA |
| HBG1/2 Gene and Promoter Sequencing method(s): ◦ Sequencing, Capillary (Sanger) Cincinnati Children's Hospital Medical Center, Molecular Genetics Laboratory - Cincinnati, OH, USA |
| HBG2 method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Fulgent Diagnostics - Temple City, CA, USA |
| Hereditary persistence of fetal hemoglobin method(s): ◦ Sequencing, Capillary (Sanger) Centogene AG, Rare Disease Company - Rostock, Germany |
| Cyanosis, transient neonatal method(s): ◦ Sequencing, Capillary (Sanger) Centogene AG, Rare Disease Company - Rostock, Germany |