| 620306 | Hbg1 | hemoglobin subunit gamma 1 | ENCODES a protein that exhibits heme binding; hemoglobin alpha binding; protein-containing complex binding; INVOLVED IN negative regulation of transcription by RNA polymerase II (ortholog); oxygen transport (ortholog); ASSOCIATED WITH Chloracne (ortholog); delta beta-thalassemia (ortholog); Parkinso n's disease (ortholog); FOUND IN hemoglobin complex; INTERACTS WITH 17beta-estradiol; 2,2',5,5'-tetrachlorobiphenyl; 3,3',5-triiodo-L-thyronine | 1 | 167683760 | 167685315 | Rat | 67 | symbol , PhenoGen | gene, protein-coding, VALIDATED [RefSeq] |
| 1345458 | HBG1 | hemoglobin subunit gamma 1 | The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two alpha chains constitute fetal hemoglobin (HbF) which is normally replaced by adult hemoglobin (HbA) at birth. In some bet a-thalassemias and related conditions, gamma chain production continues into adulthood. The two types of gamma chains differ at residue 136 where glycine is found in the G-gamma product (HBG2) and alanine is found in the A-gamma product (HBG1). The former is predominant at birth. The order of the genes in the beta-globin cluster is: 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008] | 11 | 5248269 | 5249857 | Human | 112 | symbol , COSMIC , description , Human Proteome Map | gene, protein-coding, REVIEWED [RefSeq] |
| 285280265 | hbg1 | | | | | | Tropical Clawed Frog | | symbol | gene, null |
| 285225638 | hbg1.L | | | | | | African Clawed Frog | | symbol | gene, null |
| 733957 | ACSBG1 | acyl-CoA synthetase bubblegum family member 1 | The protein encoded by this gene possesses long-chain acyl-CoA synthetase activity. It is thought to play a central role in brain very long-chain fatty acids metabolism and myelinogenesis. [provided by RefSeq, Jul 2008] | 15 | 78167468 | 78234565 | Human | 120 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 11759404 | LOC100982657 | hemoglobin subunit gamma-1 | ENCODES a protein that exhibits haptoglobin binding (inferred); heme binding (inferred); hemoglobin alpha binding (inferred); INVOLVED IN cellular oxidant detoxification (inferred); hydrogen peroxide catabolic process (inferred); oxygen transport (inferred); FOUND IN blood microparticle (inferred); haptoglobin-hemoglobin complex (inferred); hemoglobin complex (inferred) | 11 | 5397268 | 5399048 | Bonobo | 21 | old_gene_symbol | gene, protein-coding, MODEL [RefSeq] |
| 12373846 | LOC485255 | hemoglobin subunit epsilon-2 | ENCODES a protein that exhibits heme binding (inferred); metal ion binding (inferred); oxygen binding (inferred); INVOLVED IN oxygen transport (inferred); ASSOCIATED WITH acute kidney failure (ortholog); Cyanosis (ortholog); delta beta-thalassemia (ortholog); FOUND IN hemoglobin complex (inferred) | 21 | 28193163 | 28194746 | Dog | 26 | old_gene_symbol | gene, protein-coding, MODEL [RefSeq] |
| 1351638 | HBG2 | hemoglobin subunit gamma 2 | The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two alpha chains constitute fetal hemoglobin (HbF) which is normally replaced by adult hemoglobin (HbA) at birth. In some bet a-thalassemias and related conditions, gamma chain production continues into adulthood. The two types of gamma chains differ at residue 136 where glycine is found in the G-gamma product (HBG2) and alanine is found in the A-gamma product (HBG1). The former is predominant at birth. The order of the genes in the beta-globin cluster is: 5'- epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008] | 11 | 5253188 | 5254781 | Human | 96 | description | gene, protein-coding, REVIEWED [RefSeq] |
| 1617625 | Hbb-bh0 | hemoglobin, beta, pseudogene bh0 | Enables hemoglobin alpha binding activity. Predicted to be involved in hydrogen peroxide catabolic process. Part of hemoglobin complex. Human ortholog(s) of this gene implicated in delta beta-thalassemia and sickle cell anemia. Orthologous to human HBG1 (hemoglo bin subunit gamma 1) and HBG2 (hemoglobin subunit gamma 2). [provided by Alliance of Genome Resources, Apr 2025] | | | | Mouse | 18 | description | gene, pseudo, INFERRED [RefSeq] |
| 1550622 | Hbb-bh1 | hemoglobin Z, beta-like embryonic chain | Predicted to enable several functions, including heme binding activity; hemoglobin alpha binding activity; and oxygen binding activity. Predicted to contribute to haptoglobin binding activity and peroxidase activity. Acts upstream of or within negative regulation of transcription by RNA polymerase I I. Predicted to be part of haptoglobin-hemoglobin complex and hemoglobin complex. Is expressed in several structures, including aorta-gonad-mesonephros; extraembryonic component; genitourinary system; hemolymphoid system; and tail bud. Human ortholog(s) of this gene implicated in delta beta-thalassemia and sickle cell anemia. Orthologous to human HBG1 (hemoglobin subunit gamma 1) and HBG2 (hemoglobin subunit gamma 2). [provided by Alliance of Genome Resources, Apr 2025] | 7 | 103490845 | 103492369 | Mouse | 86 | description | gene, protein-coding, VALIDATED [RefSeq] |
