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UCSC Genes

BSND (uc001cye.3) at chr1:55464617-55474465 - Homo sapiens Bartter syndrome, infantile, with sensorineural deafness (Barttin) (BSND), mRNA.
CLCNKB (uc001axx.5) at chr1:16370231-16383821 - Homo sapiens chloride channel, voltage-sensitive Kb (CLCNKB), transcript variant 1, mRNA.
SGK3 (uc003xwr.3) at chr8:67624653-67774257 - Homo sapiens serum/glucocorticoid regulated kinase family, member 3 (SGK3), transcript variant 3, mRNA.
SGK3 (uc003xwt.3) at chr8:67687416-67774257 - Homo sapiens serum/glucocorticoid regulated kinase family, member 3 (SGK3), transcript variant 1, mRNA.
CLCNKA (uc001axu.3) at chr1:16348486-16360545 - Homo sapiens chloride channel, voltage-sensitive Ka (CLCNKA), transcript variant 1, mRNA.
SGK3 (uc003xwp.3) at chr8:67579787-67774257 - Homo sapiens SGK3 readthrough (SGK3), mRNA.
SGK1 (uc003qen.4) at chr6:134490384-134496034 - Homo sapiens serum/glucocorticoid regulated kinase 1 (SGK1), transcript variant 1, mRNA.

NCBI RefSeq genes, curated subset (NM_*, NR_*, NP_* or YP_*)

NM_057176.3 at chr1:55464606-55482845

RefSeq Genes

BSND at chr1:55464606-55482845 - (NM_057176) barttin

Non-Human RefSeq Genes

BSND at chr1:55464606-55476462 - (NM_001133279) barttin
BSND at chr1:55464860-55474301 - (NM_001082221) barttin
BSND at chr1:55464843-55474301 - (NM_001193084) barttin
Bsnd at chr1:55464854-55474304 - (NM_138979) barttin
Bsnd at chr1:55464854-55474304 - (NM_080458) barttin

Basic Gene Annotation Set from GENCODE Version 45lift37 (Ensembl 111)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 45lift37 (Ensembl 111)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 44lift37 (Ensembl 110)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 44lift37 (Ensembl 110)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 43lift37 (Ensembl 109)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 43lift37 (Ensembl 109)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 42lift37 (Ensembl 108)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 42lift37 (Ensembl 108)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 41lift37 (Ensembl 107)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 41lift37 (Ensembl 107)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 40lift37 (Ensembl 106)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 40lift37 (Ensembl 106)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 39lift37 (Ensembl 105)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 39lift37 (Ensembl 105)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 38lift37 (Ensembl 104)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 38lift37 (Ensembl 104)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 37lift37 (Ensembl 103)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 37lift37 (Ensembl 103)

BSND at chr1:55464606-55482845

Basic Gene Annotation Set from GENCODE Version 36lift37 (Ensembl 102)

BSND at chr1:55464606-55482845

Comprehensive Gene Annotation Set from GENCODE Version 36lift37 (Ensembl 102)

BSND at chr1:55464606-55482845

International Knockout Mouse Consortium Genes Mapped to Human Genome

Bsnd_25043 at chr1:55464617-55474465
Bsnd_25044 at chr1:55464617-55474465
Bsnd_25045 at chr1:55464617-55474465
Bsnd_25046 at chr1:55464617-55474465
Bsnd_79173 at chr1:55464617-55474465
Bsnd_89458 at chr1:55464617-55474465

Human Aligned mRNA Search Results

AY034632 - Homo sapiens barttin (BSND) mRNA, complete cds.
BC103898 - Homo sapiens Bartter syndrome, infantile, with sensorineural deafness (Barttin), mRNA (cDNA clone MGC:119283 IMAGE:40005137), complete cds.
BC103899 - Homo sapiens Bartter syndrome, infantile, with sensorineural deafness (Barttin), mRNA (cDNA clone MGC:119284 IMAGE:40005138), complete cds.
BC103900 - Homo sapiens Bartter syndrome, infantile, with sensorineural deafness (Barttin), mRNA (cDNA clone MGC:119285 IMAGE:40005139), complete cds.

Non-Human Aligned mRNA Search Results

AJ421029 - Rattus norvegicus mRNA for barttin (bsnd gene).
BC081725 - Rattus norvegicus Bartter syndrome, infantile, with sensorineural deafness (Barttin), mRNA (cDNA clone MGC:93168 IMAGE:7127281), complete cds.
AF391088 - Mus musculus barttin (Bsnd) mRNA, complete cds.
BC038287 - Mus musculus Bartter syndrome, infantile, with sensorineural deafness (Barttin), mRNA (cDNA clone MGC:47291 IMAGE:4221532), complete cds.

Ensembl Genes

BSND at chr1:55464606-55476556 - (ENST00000371265)

GeneReviews

BSND at chr1:55464606-55482845

Vega Protein-Coding Annotations

OTTHUMT00000022213 at chr1:55464606-55474656

HUGO Gene Nomenclature

BSND at chr1:55464607-55482845
BSNDP1 at chr20:25764190-25764555
BSNDP2 at chr20:25825858-25826501
BSNDP3 at chr20:26052625-26052987
BSNDP4 at chr7:57698432-57698818

gnomAD Loss of Function Metrics by Gene

BSND at chr1:55464606-55476556

gnomAD Loss of Function Metrics by Transcript

ENST00000371265 at chr1:55464606-55476556