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Ссылки на запись Gene: [19q132/APOC2] apolipoprotein C-II (lipoprotein lipase activator); lipase D activator (apolipoprotein C-II); hyperlipoproteinemia, type I-B (C-II anapolipoproteinemia);
- Gene: [19q131/RYR1] ryanodine receptor 1 (skeletal muscle; calcium release channel); Ca++ release channel of sarcoplasmic reticulum; malignant hyperthermia susceptibility 1 (King syndrome; MHS1; MIM:145600); central core disease of muscle (
- Gene: [19q132/APOC1P1] apolipoprotein C-I pseudogene 1;
- Gene: [19q132/APOC1] apolipoprotein C-I;
- Gene: [19q132/APOE] apolipoprotein E; hyperlipoproteinemia, type III; [APOE1 HPL3
]
- Gene: [19q132/ATP1A3] ATPase, Na+,K+ transporting, alpha 3 polypeptide;
- Gene: [19q132/BCL3] B-cell chronic lymphatic leukemia 3 (B-CLL: lymphoma 3); [BCL4 D19S37
]
- Gene: [19q132/CYP2A6] cytochrome P450, subfamily IIA (phenobarbital-inducible), polypeptide 6; coumarin 7-hydroxilase (microsomal; cytochrome P450-IIA3; MIM:122720);
- Gene: [19q132/LU] Lutheran blood group; B-cell adhesion molecule (BCAM); Auberger B antigen; antigen MSK19 (gp95; monoclonal antibody F8); [BCAM MSK19
]
- Gene: [19q133/CKM] creatine kinase, muscle form;
- Gene: [19q133/DMPK] myotonic distrophy protein kinase; dystrophia myotonia;
- Gene: [19q133/ERCC1] excision repair cross-complementing rodent repair deficiency, complementation group 1; [UV20
]
- Gene: [19q133/ERCC2] excision repair cross-complementing rodent repair deficiency, complementation group 2; xeroderma pigmentosum, complementation group D (MIM:278730); trichothiodystrophy (ichthyosiform erytroderma) (MIM:601675); [XPD TTD
- Gene: [19q133/FUT2] fucosyltransferase 2 (secretor status included); secretor factor of ABH system (ABH secretion);
- Gene: [19q134/PRKCG] protein kinase C, gamma polypeptide;
- Апо E-Ген (ген аполипопротеина E)
- Ген апо В: полиморфизм в московской популяции
- ген аполипопротеина CII
