Gene: CFTR

Alternate names for this Gene: ABC35|ABCC7|CF|CFTR/MRP|MRP7|TNR-CFTR|dJ760C5.1

Gene Summary: This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. The encoded protein functions as a chloride channel, making it unique among members of this protein family, and controls ion and water secretion and absorption in epithelial tissues. Channel activation is mediated by cycles of regulatory domain phosphorylation, ATP-binding by the nucleotide-binding domains, and ATP hydrolysis. Mutations in this gene cause cystic fibrosis, the most common lethal genetic disorder in populations of Northern European descent. The most frequently occurring mutation in cystic fibrosis, DeltaF508, results in impaired folding and trafficking of the encoded protein. Multiple pseudogenes have been identified in the human genome.

Gene is located in Chromosome: 7

Location in Chromosome : 7q31.2

Description of this Gene: CF transmembrane conductance regulator

Type of Gene: protein-coding

Gene: LOC105375467

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

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Description of this Gene:

Type of Gene:

Gene: WNT2

Alternate names for this Gene: INT1L1|IRP

Gene Summary: This gene is a member of the WNT gene family. The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. Alternatively spliced transcript variants have been identified for this gene.

Gene is located in Chromosome: 7

Location in Chromosome : 7q31.2

Description of this Gene: Wnt family member 2

Type of Gene: protein-coding