kcnk13b

Ensembl ID:
ENSDARG00000043557
ZFIN ID:
ZDB-GENE-040724-105
Description:
potassium channel, subfamily K, member 13b [Source:RefSeq peptide;Acc:NP_001020654]
Human Orthologue:
KCNK13
Human Description:
potassium channel, subfamily K, member 13 [Source:HGNC Symbol;Acc:6275]
Mouse Orthologue:
Kcnk13
Mouse Description:
potassium channel, subfamily K, member 13 Gene [Source:MGI Symbol;Acc:MGI:2384976]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa8470 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa8470
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000005244 Nonsense 104 412 1 2
Genomic Location (Zv9):
Chromosome 20 (position 16743825)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 16803778
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ATCCGCGTGGACGCRACCCGCGCGCGCTGGGRTTTTGCAGGAGCTTTTTA[T/A]TTCGTCGGAACTGTGGTTTCAACTATCGGTGRGTTCTCTCGAGATAACCK
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

  • Mortality among heart failure patients: Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. (View Study)

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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