right O cromossoma 13 é um dos 23 pares de cromossomas do cariótipo humano.
Genes Gene DescriçãoATP7BATPase, Cu++ transporting, beta polypeptide (Wilson disease)BRCA2breast cancer 2, early onsetCARKDCarbohydrate Kinase Domain Containing Protein (Unknown Function)EDNRBendothelin receptor type BGJB2gap junction protein, beta 2, 26kDa (connexin 26)GJB6gap junction protein, beta 6 (connexin 30)HTR2A5-HT2A receptorPCCApropionyl Coenzyme A carboxylase, alpha polypeptideRB1retinoblastoma 1 (including osteosarcoma)FLT1Fms related tyrosine kinase 1 (Vascular endothelial growth factor receptor 1)SLITRK1mutation in this gene causes some (although very few) cases of Tourette syndrome and trichotillomaniaSOX21Transcription factor SOX-21 is a protein that in humans is encoded by the SOX21; its disruption can lead to types of alopecia in mice.
Doenças Trissomia 13, ou Síndrome de Patau Retinoblastoma
Categoria:Genética humana