Genetics - Chromosome 1
Introduction
Chromosome territories (interphase) | Chromosome (Chromatin) structure (mitosis) |
Human Chromosomes: 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | 21 | 22 | X | Y |
Some Recent Findings
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More recent papers |
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This table allows an automated computer search of the external PubMed database using the listed "Search term" text link.
More? References | Discussion Page | Journal Searches | 2019 References | 2020 References Search term: Chromosome 1 |
Development Genes
BMP
Table - Human Bmp Family | ||||
Approved Symbol |
Approved Name | Previous Symbols |
Synonyms | Chromosome |
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BMP8A | bone morphogenetic protein 8a | 1p34.3 | ||
BMP8B | bone morphogenetic protein 8b | BMP8 | OP-2 | 1p34.2 |
Human BMP Family | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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WNT
Table - Human Wnt Family | ||||
Approved Symbol |
Approved Name | Previous Symbols |
Synonyms | Chromosome |
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WNT2B | Wnt family member 2B | WNT13 | XWNT2 | 1p13.2 |
WNT3A | Wnt family member 3A | 1q42.13 | ||
WNT9A | Wnt family member 9A | WNT14 | 1q42.13 | |
Links: Developmental Signals - Wnt | OMIM Wnt1 | HGNC | Bmp Family | Fgf Family | Pax Family | R-spondin Family | Sox Family | Tbx Family | Wnt Family |
Human WNT Family | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Abnormalities=
ICD-11 LD44 Deletions of the autosomes |
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The 1p36 deletion syndrome comprises a phenotypic presentation that includes central nervous system, cardiac, craniofacial, and airway anomalies. A single patient study identified a persistent buccopharyngeal membrane and unidentifiable larynx.[2]
External Links
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Idiogram Chromosome Banding - The term refers to the light and dark pattern, seen after staining with a dye, of individual chromosomes identified in metaphase. It is only in meiosis and mitosis during metaphase that chromosomes can be easily identified, during the normal cell life (interphase) the chromosomes are unravelled and distributed within the nucleus in chromosome territories. A band is that part of a chromosome which is clearly distinguishable from nearby regions by appearing darker or brighter with one or more banding techniques. | |
Genetic abnormality locations: 1-4 | 5-8 | 9-12 | 13-16 | 17-20 | 21-XY | sSMC | |
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Links: Genetics | Abnormal Development - Genetic |
Cite this page: Hill, M.A. (2024, May 15) Embryology Genetics - Chromosome 1. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Genetics_-_Chromosome_1
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
Cite this page: Hill, M.A. (2024, May 15) Embryology Genetics - Chromosome 1. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Genetics_-_Chromosome_1
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
- ↑ Zhang G, Zhao J, Yi J, Luan Y & Wang Q. (2016). Association Between Gene Polymorphisms on Chromosome 1 and Susceptibility to Pre-Eclampsia: An Updated Meta-Analysis. Med. Sci. Monit. , 22, 2202-14. PMID: 27348238
- ↑ Ferril GR, Barham HP & Prager JD. (2014). Novel airway findings in a patient with 1p36 deletion syndrome. Int. J. Pediatr. Otorhinolaryngol. , 78, 157-8. PMID: 24290305 DOI.