HBAP1
Hemoglobin, alpha pseudogene 1, also known as HBAP1, is a human gene.[2]
| HBAP1 | |||||||
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| Aliases | HBAP1, HBA-T1, HBA3, HBA3P, hemoglobin subunit alpha pseudogene 1 | ||||||
| External IDs | GeneCards: HBAP1 | ||||||
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| Species | Human | Mouse | |||||
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| Location (UCSC) | n/a | n/a | |||||
| PubMed search | [1] | n/a | |||||
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References
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: HBAP1 hemoglobin, alpha pseudogene 1".
Further reading
- Proudfoot NJ, Brownlee GG (1976). "3' non-coding region sequences in eukaryotic messenger RNA". Nature. 263 (5574): 211–4. Bibcode:1976Natur.263..211P. doi:10.1038/263211a0. PMID 822353. S2CID 4211839.
- Fougerousse F, Meloni R, Roudaut C, Beckmann JS (1992). "Dinucleotide repeat polymorphism at the human hemoglobin alpha-1 pseudo-gene (HBAP1)". Nucleic Acids Res. 20 (5): 1165. doi:10.1093/nar/20.5.1165. PMC 312136. PMID 1549498.
- Hess J, Perez-Stable C, Wu GJ, et al. (1985). "End-to-end transcription of an Alu family repeat. A new type of polymerase-III-dependent terminator and its evolutionary implication". J. Mol. Biol. 184 (1): 7–21. doi:10.1016/0022-2836(85)90039-7. PMID 2411938.
- Safaya S, Rieder RF (1988). "Dysfunctional alpha-globin gene in hemoglobin H disease in blacks. A dinucleotide deletion produces a frameshift and a termination codon". J. Biol. Chem. 263 (9): 4328–32. PMID 2831226.
- Marotta CA, Forget BG, Weissman SM, et al. (1974). "Nucleotide sequences of human globin messenger RNA". Proc. Natl. Acad. Sci. U.S.A. 71 (6): 2300–4. Bibcode:1974PNAS...71.2300M. doi:10.1073/pnas.71.6.2300. PMC 388440. PMID 4135409.
- Perez-Stable C, Ayres TM, Shen CK (1984). "Distinctive sequence organization and functional programming of an Alu repeat promoter". Proc. Natl. Acad. Sci. U.S.A. 81 (17): 5291–5. Bibcode:1984PNAS...81.5291P. doi:10.1073/pnas.81.17.5291. PMC 391689. PMID 6089189.
- Proudfoot NJ, Gil A, Maniatis T (1983). "The structure of the human zeta-globin gene and a closely linked, nearly identical pseudogene". Cell. 31 (3 Pt 2): 553–63. doi:10.1016/0092-8674(82)90311-7. PMID 6297773. S2CID 36907055.
- Goodbourn SE, Higgs DR, Clegg JB, Weatherall DJ (1983). "Molecular basis of length polymorphism in the human zeta-globin gene complex". Proc. Natl. Acad. Sci. U.S.A. 80 (16): 5022–6. Bibcode:1983PNAS...80.5022G. doi:10.1073/pnas.80.16.5022. PMC 384180. PMID 6308667.
- Orkin SH, Michelson A (1980). "Partial deletion of the alpha-globin structural gene in human alpha-thalassaemia". Nature. 286 (5772): 538–40. Bibcode:1980Natur.286..538O. doi:10.1038/286538a0. PMID 7402334. S2CID 4251647.
- Proudfoot NJ, Maniatis T (1980). "The structure of a human alpha-globin pseudogene and its relationship to alpha-globin gene duplication". Cell. 21 (2): 537–44. doi:10.1016/0092-8674(80)90491-2. PMID 7407925. S2CID 54360867.
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