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NKX2-5
NK2 homeobox 5CSX, CSX1, NKX2.5, NKX2E, NKX4-1
This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Top validated antibodies |
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| Invitrogen Antibodies |  PA5-49431 |
7 references | Polyclonal |
WB
ICC
IHC
FC
OA
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| Proteintech Group | 13921-1-AP |
13 references | Polyclonal |
WB
EL
IHC
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| Novus Biologicals | NBP1-51953 |
1 references | Polyclonal |
WB
EL
ICC
IHC
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| antibodies-online | ABIN441557 |
2 references | Polyclonal |
WB
ICC
IHC
FC
|
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| GeneTex | GTX133155 |
3 references | Polyclonal |
WB
ICC
IHC
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