KCNA2 (2 of 2)

Ensembl ID:
ENSDARG00000002241
Description:
potassium voltage-gated channel, shaker-related subfamily, member 2 [Source:HGNC Symbol;Acc:6220]
Human Orthologue:
KCNA2
Human Description:
potassium voltage-gated channel, shaker-related subfamily, member 2 [Source:HGNC Symbol;Acc:6220]
Mouse Orthologue:
Kcna2
Mouse Description:
potassium voltage-gated channel, shaker-related subfamily, member 2 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa20814 Nonsense Mutation detected in F1 DNA During 2017
sa44645 Nonsense Mutation detected in F1 DNA During 2017
sa2280 Nonsense F2 line generated During 2017

Mutation Details

Allele Name:
sa20814
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
ENSDART00000027398 Nonsense 91 493 1 2
Genomic Location (Zv9):
Chromosome 6 (position 49358297)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 49414373
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TACTTTTTTGACAGAAACCGCCCCAGCTTTGACGCCATTCTCTATTACTA[T/A]CAATCAGGCGGAAGGTTGCGGAGACCAGTCAATGTCACATTGGATGTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44645
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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000027398 Nonsense 113 493 1 2
Genomic Location (Zv9):
Chromosome 6 (position 49358361)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GGTTGCGGAGACCAGTCAATGTCACATTGGATGTGTTCTCAGAGGAGATT[C/T]GATTTTATGAGCTCGGAGACGAAGCCATTGAGATTTTCAGGGAGGATGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2280
Current Status:
F2 line generated
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
ENSDART00000027398 Nonsense 154 493 1 2
Genomic Location (Zv9):
Chromosome 6 (position 49358486)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 49414562
KASP Assay ID:
554-2435.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CCATTGCCTGACAATGAGTTTCAGAAGCAGGTCTGGTTGCTGTTCGAGTA[T/A]CCAGAAAGTTCAGGGCCAGCCAGGATTATAGCAATCRTATCTGTAATGGT
Associated Phenotype:
Not determined

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