Chromosoma 4 (homo)

Chromosoma 4 humanum est uno ex viginti tribus paribus in hominibus quibus de consuetudine horum chromosomatum duo exempla sunt. Numerus basium conexarum est 191 263 063 quod est 6.2 centesimae omnium^[1]. Plures morbi genetici e mutationibus chromosomatis 4 oriuntur.

Gena

Inter alia haec gena in chromosomate humani 4 locata sunt:

CSN2 - beta caseinum (lac)
FGFR3 — Hypochondroplasia (4p16.3)
GRIA2 — receptorium ionotropicum glutamati (AMPA) 2 (4q32-33)
SEPT11 — septinum 11
SNCA — Alpha-synucleinum
UCHL1 — ubiquitini thiolesterasis (oncogenum)

Deletio partium chromosomatis

Deletio 4p- (syndroma Wolf–Hirschhorn)

Deletio chromosomalis 4p16.3 syndroma Wolf–Hirschhorn vocatur. Symptomata - inter alia - sunt microcephalia, nasus latus, perturbationes procreationis dentium.

Notae

↑ Descriptio chromosomatis 4.

Nexus interni

Nexus externi

Chromosoma 4 et Human Genome Project: http://web.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chromo04.shtml

Chromosomata hominis


Chromosoma • chromosoma 1 • chromosoma 2 • chromosoma 3 • chromosoma 4 • chromosoma 5 • chromosoma 6 • chromosoma 7 • chromosoma 8 • chromosoma 9 • chromosoma 10 • chromosoma 11 • chromosoma 12 • chromosoma 13 • chromosoma 14 • chromosoma 15 • chromosoma 16 • chromosoma 17 • chromosoma 18 • chromosoma 19 • chromosoma 20 • chromosoma 21 • chromosoma 22 • chromosoma X • chromosoma Y

[1] Descriptio chromosomatis 4.

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