Cromossoma 13: diferenças entre revisões
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Linha 3:
== Genes ==
{|class = "wikitable"
* ATP7B: ATPase, Cu++ transporting, beta polypeptide (Wilson disease)▼
!Gene !!Descrição
* BRCA2: breast cancer 2, early onset▼
|-
* CARKD: Carbohydrate Kinase Domain Containing Protein (Unknown Function)▼
|ATP7B
* EDNRB: endothelin receptor type B▼
* GJB2: gap junction protein, beta 2, 26kDa (connexin 26)▼
|-
* GJB6: gap junction protein, beta 6 (connexin 30)▼
|BRCA2
* HTR2A: 5-HT<sub>2A</sub> receptor▼
* PCCA: propionyl Coenzyme A carboxylase, alpha polypeptide▼
|-
* RB1: retinoblastoma 1 (including osteosarcoma)▼
|CARKD
* 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.▼
|EDNRB
|-
|GJB2
|-
|GJB6
|-
|HTR2A
|-
|PCCA
|-
|RB1
|-
|FLT1
|-
|SLITRK1
▲
|-
|SOX21
▲
|}
== Doenças ==
* [[Síndrome de Patau|Trissomia 13]], ou [[Síndrome de Patau]]
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