Symbol Name ID

Slc17a6 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6 MGI:2156052

Reference

J:131365 Dubreuil V, Ramanantsoa N, Trochet D, Vaubourg V, Amiel J, Gallego J, Brunet JF, Goridis C, A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea, and specific loss of parafacial neurons. Proc Natl Acad Sci U S A. 2008 Jan 22;105(3):1067-72

Indicates gene expression was analyzed but not necessarily detected.

Age	P
Immunohistochemistry (section)
In situ RNA (section)
Immunohistochemistry (whole mount)
In situ RNA (whole mount)
In situ reporter (knock in)
Northern blot
Western blot
RT-PCR
cDNA clones
RNase protection
Nuclease S1
Primer Extension