Cromossoma 9 – Wikipédia, a enciclopédia livre
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O cromossoma 9 é um dos 23 pares de cromossomas do cariótipo humano.
Genes
[editar | editar código-fonte]Gene | Descrição |
---|---|
ABO | ABO histo-blood group glycosyltransferases |
ADAMTS13 | ADAM metallopeptidase with thrombospondin type 1 motif, 13 |
ALAD | aminolevulinate, delta-, dehydratase |
ALS4 | amyotrophic lateral sclerosis 4 |
ASS | argininosuccinate synthetase |
CCL21 | chemokine (C-C motif) ligand 21, SCYA21 |
CCL27 | chemokine (C-C motif) ligand 27, SCYA27 |
COL5A1 | collagen, type V, alpha 1 |
ENG | endoglin (Osler-Rendu-Weber syndrome 1) |
FXN | frataxin |
GALT | galactose-1-phosphate uridylyltransferase |
GLE1L | |
Nucleoporin GLE1 | |
GRHPR | glyoxylate redasductase/hydroxypyruvate reductase |
IKBKAP | inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein |
TGFBR1 | transforming growth factor beta, receptor type I |
TMC1 | transmembrane channel-like 1 |
TSC1 | tuberous sclerosis 1 |