BSND (Barttin, Bartter Syndrome, Infantile, with Sensorineural Deafness, BART, DFNB73, MGC119283, MGC119284, MGC119285)
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Catalog numberMBS6000490
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PricePlease ask
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Size0,05 mg
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Other sizeplease contact us to order other different size
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Gene target
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Gene symbolBSND, ARL2BP
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Short nameBSND (Barttin, Bartter Syndrome, Infantile, with Sensorineural Deafness, BART, DFNB73, MGC119283, MGC119284, MGC119285)
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Alternative nameBSND (Barttin, Bartter Syndrome, Infantile, including Sensorineural Deafness, BART, DFNB73, MGC119283, MGC119284, MGC119285)
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Diseasesyndrome
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Gene info
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Identity
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Gene
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Long gene namebarttin CLCNK type accessory subunit beta
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Synonyms gene
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Synonyms gene name
- deafness, autosomal recessive 73
- Bartter syndrome, infantile, with sensorineural deafness (Barttin)
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Synonyms
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GenBank acession
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Locus
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Discovery year2004-01-28
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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Classification
- Chloride voltage-gated channels
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VEGA ID
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Locus Specific Databases
Gene info
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Identity
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Gene
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Long gene nameADP ribosylation factor like GTPase 2 binding protein
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Synonyms gene
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Synonyms gene name
- retinitis pigmentosa 66 (autosomal recessive)
- ADP-ribosylation factor-like 2 binding protein
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Synonyms
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Synonyms name
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GenBank acession
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Locus
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Discovery year2004-02-12
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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VEGA ID
MeSH Data
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Name
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ConceptScope note: Identification of proteins or peptides that have been electrophoretically separated by blot transferring from the electrophoresis gel to strips of nitrocellulose paper, followed by labeling with antibody probes.
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Tree numbers
- E05.196.401.143
- E05.301.300.096
- E05.478.566.320.200
- E05.601.262
- E05.601.470.320.200
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Qualifiersethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data