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