-
channel Kb, also
known as
CLCNKB, is a
protein which in
humans is
encoded by the
CLCNKB gene.
Chloride channel Kb (
CLCNKB) is a
member of the CLC family...
-
Gitelman syndrome cases can be
attributed to disease-causing
variants in the
CLCNKB gene. Disease-causing
variants in this gene are
responsible for Bartter...
- ROMK/KCNJ1
thick ascending limb K+
channel classic Bartter's
syndrome type 3
CLCNKB Cl−
channel Bartter's
syndrome with
sensorineural deafness type 4 BSND Cl−...
- CLCN4, CLCN5, CLCN6, CLCN7, CLCNKA,
CLCNKB BSND -
encodes barttin,
accessory subunit beta for
CLCNKA and
CLCNKB Members of
Epithelial Chloride Channel...
- encomp**** the
syndromes caused by
mutations in CLDN16, CLDN19, CASR or
CLCNKB. In
these diseases,
reabsorption of
divalent cations (such as magnesium...
- HGNC:2024 P51797 3118 CLCN7 HGNC:2025 P51798 3119
CLCNKA HGNC:2026 P51800 3120
CLCNKB HGNC:2027 P51801 3121 CLDN1 HGNC:2032 O95832 3122 CLDN2 HGNC:2041 P57739...
-
vicinity to two
other kidney-specific
chloride channel genes,
CLCNKA and
CLCNKB.
Chloride channel GRCh38:
Ensembl release 89: ENSG00000011021 – Ensembl...
- 2008). "****ociation
study of
variants in two ion-channel
genes (TSC and
CLCNKB) and
hypertension in two
ethnic groups in
Northwest China".
Clinica Chimica...
- and pot****ium
recycling in the
inner ear. The gene is
highly similar to
CLCNKB,
which is
located 10 kb
downstream from this gene.
CLCNKA encodes one of...
-
mutations in CLCN7 can lead to
osteopetrosis (OMIM: 259700), and
mutations in
CLCNKB can lead to
Bartter syndrome (OMIM: 241200). PDB: 2nye;
Rudolph MJ, Amodeo...
