Cromossoma 13

O cromossoma 13 é um dos 23 pares de cromossomas do cariótipo humano.

Par de cromossoma 13

Genes

Gene	Descrição
ATP7B	ATPase, Cu++ transporting, beta polypeptide (Wilson disease)
BRCA2	breast cancer 2, early onset
CARKD	Carbohydrate Kinase Domain Containing Protein (Unknown Function)
EDNRB	endothelin receptor type B
GJB2	gap junction protein, beta 2, 26kDa (connexin 26)
GJB6	gap junction protein, beta 6 (connexin 30)
HTR2A	5-HT2A receptor
PCCA	propionyl Coenzyme A carboxylase, alpha polypeptide
RB1	retinoblastoma 1 (including osteosarcoma)
FLT1	Fms related tyrosine kinase 1 (Vascular endothelial growth factor receptor 1)
SLITRK1	mutation in this gene causes some (although very few) cases of Tourette syndrome and trichotillomania
SOX21	Transcription 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