KCNK9
This gene encodes a protein that performs as a pH-dependent potassium channel and has two pore-forming P domains and several transmembrane sections. This gene has been found to be amplified and overexpressed in a variety of human carcinomas. This gene expresses preferentially from the maternal allele and is imprinted in the brain. This gene's mutation has been linked to Birk-Barel dysmorphism syndrome.
| Full Name | Potassium two pore domain channel subfamily K member 9 |
| Gene ID | Human: 51305 Mouse: 223604 Rat: 84429 Monkey: 100425983 |
| UniProt ID | Human: Q9NPC2 Mouse: Q3LS21 Rat: Q9ES08 Monkey: A0A1D5RJ09 |
| Alternative Names | KT3.2; TASK3; BIBARS; K2p9.1; TASK-3; TASK32; potassium channel subfamily K member 9; TWIK-related acid-sensitive K(+) channel 3; TWIK-related acid-sensitive K+ 3; acid-sensitive; potassium channel protein TASK-3; potassium 2-pore domain leak channel TASK3; potassium channel, two pore domain subfamily K, member 9; two pore K(+) channel KT3.2; two pore potassium channel KT3.2; KCNK9; Potassium two pore domain channel subfamily K member 9 |
Product List
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Magic™ mPro Human KCNK9 Cell Line
[CAT#: S01YF-1122-KX128]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNK9 Target Family: Two P Domain Potassium Channel Assay Target Protein Species: Human
mProX™ Human KCNK9 Stable Cell Line
[CAT#: S01YF-1123-KX47]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNK9 Target Family: TASK Target Protein Species: Human Host Cell Type: PASMC; COS7; CHO-K1; HEK293
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