Chromosoma 9 (homo)
Chromosoma 9 humanum est uno ex viginti tribus paribus in hominibus quibus de consuetudine horum chromosomatum duo exempla sunt. Numerus basium conexarum est 140 442 298 quod est 4.6 centesimae omnium[1]. Plures morbi genetici e mutationibus chromosomatis 9 oriuntur.
Gena
recensereInter alia haec gena in chromosomate humani 9 locata sunt:
locus | coordinata | genum | proteinum | OMIM |
---|---|---|---|---|
9p24.1 | 006 215 786 — 006 257 983 | IL33 | Interleukinum 33 | 608678 |
9p21.2 | 027 546 545 — 027 573 865 | C9orf72 | Chromosomatis 9 margo lectoria aperta 72 | 614260 |
9p13.3 | 034 646 588 — 034 650 597 | GALT | Galactoso-1-phosphati uridylyltransferasis | 606999 |
9q31.1 | 101 420 559 — 101 435 779 | ALDOB | Aldolasis B (hepatica) | 612724 |
9q34.3 | 137 139 091 — 137 168 761 | GRIN1 | Receptorii NMDA subunitas NR1 | 138249 |
9q34.3 | 135 075 242 — 135 121 183 | OLFM1 | Olfactomedinum 1 | 605366 |
9q34.3 | 136 410 572 — 136 423 760 | PMPCA | Perfabricantis mitochondrialis peptidasis subunitas A | 613036 |
Notae
recensereNexus interni
- Galactosaemia
- Leuchaemia myelogenosa chronica — (t(9;22)(q34.1;q11.2) - chromosoma Philadelphiense
- Trisomia 9
Nexus externi
recensere- Chromosoma 9 et Human Genome Project: http://web.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chromo09.shtml
Chromosomata hominis