Chromosom 17

Chromosom 17 – jeden z 23 parzystych chromosomów człowieka. DNA chromosomu 17 liczy ponad 81 milionów par nukleotydów, co stanowi około 2,5-3% materiału genetycznego ludzkiej komórki. Liczbę genów chromosomu 17 szacuje się na 1 200-1 500.

Geny

ACADVL
ACTG1
ASPA
BRCA1
CBX1
COL1A1
ERBB2
FLCN
GALK1
GFAP
JUP
KCNJ2
MYO15A
NF1
PMP22
SHBG
TP53
USH1G
RAI1
RAR α
GRB7
Geny chemokin: CCL1, CCL2, CCL3, CCL4, CCL5, CCL7, CCL8, CCL11, CCL13, CCL14, CCL15, CCL16, CCL18 i CCL23.
TCF2

Choroby

Przypisy

↑ LorraineL. Potocki LorraineL. i inni, Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype, „American Journal of Human Genetics”, 80 (4), 2007, s. 633–649, DOI: 10.1086/512864, ISSN 0002-9297, PMID: 17357070, PMCID: PMC1852712 [dostęp 2023-01-24] .

Bibliografia

Gilbert F. Disease genes and chromosomes: disease maps of the human genome. Chromosome 17. „Genetic Testing”. 2. 4, s. 357-381, 1998. PMID: 10464617.
Zody MC, Garber M, Adams DJ, Sharpe T, Harrow J, Lupski JR, Nicholson C, Searle SM, Wilming L, Young SK, Abouelleil A, Allen NR, Bi W, Bloom T, Borowsky ML, Bugalter BE, Butler J, Chang JL, Chen CK, Cook A, Corum B, Cuomo CA, de Jong PJ, DeCaprio D, Dewar K, FitzGerald M, Gilbert J, Gibson R, Gnerre S, Goldstein S, Grafham DV, Grocock R, Hafez N, Hagopian DS, Hart E, Norman CH, Humphray S, Jaffe DB, Jones M, Kamal M, Khodiyar VK, LaButti K, Laird G, Lehoczky J, Liu X, Lokyitsang T, Loveland J, Lui A, Macdonald P, Major JE, Matthews L, Mauceli E, McCarroll SA, Mihalev AH, Mudge J, Nguyen C, Nicol R, O'Leary SB, Osoegawa K, Schwartz DC, Shaw-Smith C, Stankiewicz P, Steward C, Swarbreck D, Venkataraman V, Whittaker CA, Yang X, Zimmer AR, Bradley A, Hubbard T, Birren BW, Rogers J, Lander ES, Nusbaum C. DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. „Nature”. 440. 7087, s. 1045-1049, 2006. PMID.

Linki zewnętrzne

Human Genome Organisation (ang.)
Chromosom 17. ghr.nlm.nih.gov. [zarchiwizowane z tego adresu (2007-06-30)]. na stronie Genetics Home Reference (ang.)

[1] LorraineL. Potocki LorraineL. i inni, Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype, „American Journal of Human Genetics”, 80 (4), 2007, s. 633–649, DOI: 10.1086/512864, ISSN 0002-9297, PMID: 17357070, PMCID: PMC1852712 [dostęp 2023-01-24] .

[1]