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Results 1 - 10 of 233 for cls
  1. COLEC11 gene 
    ... for making a protein called collectin kidney 1 (CL-K1). This protein is involved in a series ... syndrome impair or eliminate the function of the CL-K1 protein, resulting in faulty control of cell ...
    https://medlineplus.gov/genetics/gene/colec11 - Genetics
  2. COLEC10 gene 
    ... for making a protein called collectin liver 1 (CL-L1). This protein is involved in a series ... syndrome impair or eliminate the function of the CL-L1 protein, resulting in faulty control of cell ...
    https://medlineplus.gov/genetics/gene/colec10 - Genetics
  3. SLC12A3 gene 
    ... charged atoms (ions) of sodium (Na+) and chlorine (Cl-) across cell membranes.The NCC protein is essential ... in the SLC12A3 gene and blood pressure. Na-Cl symporter NaCl electroneutral thiazide-sensitive cotransporter NCCT S12A3_ ...
    https://medlineplus.gov/genetics/gene/slc12a3 - Genetics
  4. SLC12A6 gene 
    ... for making a protein called KCC3, a K-Cl co-transporter present in several organs. This protein ... charged atoms (ions) of potassium (K) and chlorine (Cl) across the cell membrane. The positively charged potassium ...
    https://medlineplus.gov/genetics/gene/slc12a6 - Genetics
  5. SLC12A1 gene 
    ... ions) of sodium (Na+), potassium (K+), and chlorine (Cl-) into cells.The NKCC2 protein is essential for ... potassium)-chloride cotransporter 2 kidney-specific Na-K-Cl symporter Na-K-2Cl cotransporter NKCC2 S12A1_HUMAN ...
    https://medlineplus.gov/genetics/gene/slc12a1 - Genetics
  6. CLCN5 gene 
    ... function, ClC-5 is known as a H+/Cl- exchanger.ClC-5 is found primarily in the ... clC-5 CLC5 CLCK2 CLCN5_HUMAN DENTS H(+)/Cl(-) exchange transporter 5 hCIC-K2 hClC-K2 NPHL1 ...
    https://medlineplus.gov/genetics/gene/clcn5 - Genetics
  7. Coffin-Lowry syndrome 
    ... have other family members with Coffin-Lowry syndrome. CLS Mental retardation with osteocartilaginous abnormalities Genetic Testing Registry: ... Rare Disorders (NORD) ClinicalTrials.gov COFFIN-LOWRY SYNDROME; CLS PubMed Hanauer A, Young ID. Coffin-Lowry syndrome: ...
    https://medlineplus.gov/genetics/condition/coffin-lowry-syndrome - Genetics
  8. CLCN7 gene 
    ... 7 CLC7 CLCN7_HUMAN FLJ26686 FLJ39644 FLJ46423 H(+)/Cl(-) exchange transporter 7 OPTA2 OPTB4 PPP1R63 Tests of ...
    https://medlineplus.gov/genetics/gene/clcn7 - Genetics
  9. CLCN1 gene 
    The CLCN1 gene provides instructions for making a type of protein called a chloride channel. These channels, which transport negatively charged chlorine ...
    https://medlineplus.gov/genetics/gene/clcn1 - Genetics
  10. WNK1 gene 
    ... L, Meermeier NP, Rogers S, Jeunemaitre X, Yang CL, Ellison DH, Gamba G, Hadchouel J. WNK-SPAK- ... revisited: WNK1 stimulates the activity of the Na-Cl cotransporter via SPAK, an effect antagonized by WNK4. ...
    https://medlineplus.gov/genetics/gene/wnk1 - Genetics
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