Chromosoma 11 (homo)
Chromosoma 11 humanum est uno ex viginti tribus paribus in hominibus, quibus de consuetudine horum chromosomatum duo exempla sunt. Hoc chromosoma portat 134 452 384 bases conexas, quod est 4,4 centesimae omnium in genomate. Plures morbi genetici e mutationibus chromosomatis 11 oriuntur.

Gena 
Inter alia haec gena in chromosomate humani 11 locata sunt: 
 ACAT1 — acetyl-coenzymi A acetyltransferasis 1: 11q22.3-23.1 
 APOA4 — apolipoproteinum: 11q23
 BACE - beta-secretasis 1: 11q23.3
 CASP — caspasis 1 (11q22.3)
 GRIA4 — receptorium ionotropicum glutamati (AMPA) 4 (11q22-23)
 GRIK4 — receptorium ionotropicum glutamati (Kainatum) 4 (11q22.3)
 GRM5 - Receptorium metabotropicum glutamati 
 CHRM1 - Receptorium acetylcholini muscarinicum M1 (M1R) 11q12.3
 SERPING1 — inhibitor esterasis C1 (angiooedema hereditarium): 11q12.1
 TH — tyrosini hydroxylasis: 11p15.5, synthesis biologicae dopamini.

Notae 

 Autismus
 Cancer vesicae
 Cancer mammae
 Depressio
 Receptorium dopamini D2

Nexus externi 
 Chromosoma 11 et Human Genome Project: http://web.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chromo11.shtml

Chromosomata humana
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