mutant cystic fibrosis transmembrane conductance regulator, partial [H - Protein

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Mutational spectrum of CFTR in cystic fibrosis patients with gastrointestinal and hepatobiliary manifestations. [Mol Biol Rep. 2024]
Mutational spectrum of CFTR in cystic fibrosis patients with gastrointestinal and hepatobiliary manifestations.
Waheed N, Waris R, Naseer M, Razzaq A, Haider N, Shah AA, Ullah A. Mol Biol Rep. 2024 Apr 25; 51(1):573. Epub 2024 Apr 25.
Functional Consequences of CFTR Interactions in Cystic Fibrosis. [Int J Mol Sci. 2024]
Functional Consequences of CFTR Interactions in Cystic Fibrosis.
Ramananda Y, Naren AP, Arora K. Int J Mol Sci. 2024 Mar 16; 25(6). Epub 2024 Mar 16.
CFTR function is impaired in a subset of patients with pancreatitis carrying rare CFTR variants. [Pancreatology. 2024]
CFTR function is impaired in a subset of patients with pancreatitis carrying rare CFTR variants.
Angyal D, Kleinfelder K, Ciciriello F, Groeneweg TA, De Marchi G, de Pretis N, Bernardoni L, Rodella L, Tomba F, De Angelis P, et al. Pancreatology. 2024 May; 24(3):394-403. Epub 2024 Mar 10.

RefSeq genomic sequence
See the genomic reference sequence for the CFTR gene (NG_016465.4).
RefSeq protein
See the reference protein sequence for cystic fibrosis transmembrane conductance regulator (NP_000483.3).

Nucleotide
Nucleotide sequence from coding region
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mutant cystic fibrosis transmembrane conductance regulator, partial [Homo sapien...
mutant cystic fibrosis transmembrane conductance regulator, partial [Homo sapiens]
gi|693268784|gb|AIS25625.1|

Protein
1763484[uid] (1)
Taxonomy
PICSAR[gene] (43)
ClinVar
Homo sapiens protein tyrosine phosphatase, non-receptor type 3, mRNA (cDNA clone...
Homo sapiens protein tyrosine phosphatase, non-receptor type 3, mRNA (cDNA clone MGC:177380 IMAGE:9052363), complete cds
gi|219520090|gb|BC143848.1|

Nucleotide

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Protein