si:dkey-192j17.1

Ensembl ID:
ENSDARG00000088842
ZFIN ID:
ZDB-GENE-091113-38
Human Orthologue:
KCNB2
Human Description:
potassium voltage-gated channel, Shab-related subfamily, member 2 [Source:HGNC Symbol;Acc:6232]
Mouse Orthologue:
AC132603.1
Mouse Description:
potassium voltage-gated channel subfamily B member 2 [Source:RefSeq peptide;Acc:NP_001091998]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa16111 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa16111
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123450 Essential Splice Site 202 698 1 2
Genomic Location (Zv9):
Chromosome 24 (position 13469543)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 13420991
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AAAACWTTGGGWGCTTTTGGAGAAGCCAAGTTCTTCGGTTGCTGCTAAGG[T/C]AAGGCCAAGCRTCCCAATACTCATACAGKCAGATCAGTTCGACCTCAGTT
Associated Phenotype:
Not determined

GWAS

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

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

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