ATP6V1B1
|
0.400 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
By contrast, more recent studies have shown that mutations in ATP6B1, encoding the B-subtype unit of the apical H(+) ATPase, are responsible for a group of patients with autosomal recessive dRTA associated with sensorineural deafness.
|
11160790 |
2001 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Previously we have shown that mutations in two kidney-specific genes, ATP6V1B1 and ATP6V0A4, encoding the H(+)-ATPase B1 and a4 subunit isoforms, cause recessive distal renal tubular acidosis (dRTA).
|
12384298 |
2002 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
ATP6B1 gene mutations associated with distal renal tubular acidosis and deafness in a child.
|
12500243 |
2003 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis.
|
12579397 |
2003 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Our report shows that hearing loss is not always present in the syndrome of distal renal tubular acidosis with nerve deafness and the absence of hypercalciuria at diagnosis and describes a new mutation responsible for the disease in the ATP6V1B1 gene.
|
17216496 |
2007 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Several types of mutations in the ATP6V1B1 gene may cause distal renal tubular acidosis and sensorineural hearing loss.
|
17669226 |
2008 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
A homozygous mutation in the ATP6V1B1 gene, which is responsible for dRTA with early hearing loss, was detected in both siblings.
|
18386070 |
2008 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Mutations in ATP6V1B1 are associated with early onset SNHL, whereas ATP6V0A4 mutations have been described in dRTA and late-onset SNHL.
|
19639346 |
2009 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Novel ATP6V1B1 mutations in distal renal tubular acidosis and hearing loss.
|
20233014 |
2010 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Founder mutations in the ATP6V1B1 gene explain most Cypriot cases of distal renal tubular acidosis: first prenatal diagnosis.
|
20805693 |
2011 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Mutations in ATP6V1B1, encoding the B-subtype unit of the apical H(+) ATPase, and ATP6V0A4, encoding the a-subtype unit, lead to the loss of function of the apical H(+) ATPase and are usually responsible for patients with autosomal recessive dRTA often associated with early or late sensorineural deafness.
|
23114896 |
2012 |
ATP6V1B1
|
0.400 |
Biomarker
|
disease |
BEFREE |
Mutational analyses of the ATP6V1B1 and ATP6V0A4 genes in patients with primary distal renal tubular acidosis.
|
23729491 |
2013 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Our study shows that rare and family-specific variants in ATP6V1B1 are responsible for DRTA and sensorineural hearing loss syndrome in Turkey.
|
23923981 |
2013 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
We aim to identify molecular defects present in the ATP6V1B1, ATP6V0A4 and SLC4A1 genes in a Tunisian cohort, according to the following algorithm: first, ATP6V1B1 gene analysis in dRTA patients with sensorineural hearing loss (SNHL) or unknown hearing status.
|
24252324 |
2013 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
ATP6V1B1 and ATP6V0A4 genetic mutations cause recessive forms of distal renal tubular acidosis.
|
25498251 |
2014 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
These results conclusively explain these mutations in ATP6V1B1 gene resulted in structural changes causing accumulation of H(+) ions contributing to dRTA with sensorineural deafness.
|
25517796 |
2015 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The genomic deletion reported here is firstly, the only reported example of a whole gene deletion to underlie Distal Renal Tubular Acidosis, where the clinical phenotype is indistinguishable from that of other patients with ATP6V1B1 mutations; secondly, this is the first reported example of a human VAX2 mutation and associated ocular phenotype, supporting speculation in the literature that VAX2 is important for correct retinal functioning.
|
26068435 |
2015 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Primary distal renal tubular acidosis (DRTA) is a rare disease caused by loss-of-function mutations in at least three genes (ATP6V0A4, ATP6V1B1, and SLC4A1) involved in urinary distal acidification.
|
26571219 |
2016 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
In this report, we propose first line genetic testing based on screening of these two mutations both located in exon 12 of ATP6V1B1 gene in Moroccan patients with recessive form of dRTA associated to precocious hearing loss.
|
27140593 |
2018 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Mutations of the human ATP6V1B1 gene cause distal renal tubular acidosis (dRTA; OMIM #267300) often associated with sensorineural hearing impairment; however, mice with a knockout mutation of Atp6v1b1 were reported to exhibit a compensated acidosis and normal hearing.
|
28934385 |
2017 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Progressive sensorineural hearing loss develops in the majority of patients with recessive dRTA (ATP6V1B1 and ATP6V0A4 mutations).
|
28994037 |
2018 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
The patient is a heterozygote for two different mutations, one in each of the genes ATP6V0A4 and ATP6V1B1, while no deleterious variation was detected in the remaining genes responsible for the recessive form of dRTA.
|
29024829 |
2018 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Twenty-seven non-oriental patients with genetically confirmed dRTA were grouped according to the identified underlying mutations in either ATP6V1B1 (n = 10), ATP6V0A4 (n = 12), or SLC4A1 (n = 5) gene.
|
29725771 |
2018 |
ATP6V1B1
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Homozygous mutations or deletion of the ATP6V1B1 gene encoding for the B1 subunit of the vacuolar H+-ATPase leads to distal renal tubular acidosis in man and mice.
|
29843146 |
2018 |