ZMP

LOC100150068

Ensembl ID:

ENSDARG00000079491

Human Orthologue:

KCNA3

Human Description:

potassium voltage-gated channel, shaker-related subfamily, member 3 [Source:HGNC Symbol;Acc:6221]

Mouse Orthologue:

Kcna3

Mouse Description:

potassium voltage-gated channel, shaker-related subfamily, member 3 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10358	Nonsense	Available for shipment	Available now
sa33962	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa10358

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109628	Nonsense	357	483	1	1

Genomic Location (Zv9):

Chromosome 6 (position 49308870)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	49368147
GRCz11	6	49366800

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGAGGCGGAYGACCCTACATCCAGCTTCAGCAGCATCCCTGATGCTTTTT[G/A]GTGGGCTGTGGTAACCATGACTACAGTGGGCTATGGAGACATGCATCCAG

Long Flanking Sequence:

CGACAAGGACCCGACTACTGTGTCTCCTATCGCAAACGTCACTGGCCCGTTCGTGTCCAGCACTTTCACAGACCCTTTCTTTGTAATCGAGACCCTTTGCATCATCTGGTTCTCTTTTGAACTGCTCGTGCGCTTCTTCGCGTGCCCCAGCAAGGCTACTTTTTCCAAAAACATCATGAATATCATTGACATTGTGGCTATTATTCCCTATTTCATCACTCTGGGGACGGAGCTGGCTGAAAGACAAGGCAACGGTCAACAAGCCATGTCGCTGGCCATCCTCCGAGTGATCCGTCTGGTGAGGGTCTTTCGCATCTTCAAGCTCTCACGTCACTCTAAAGGCCTGCAGATCCTTGGCCAGACTCTGAAAGCCAGCATGAGGGAACTGGGACTCCTCATCTTCTTCCTCTTCATTGGGGTCATCTTGTTTTCCAGCGCCGTCTACTTTGCTGAGGCGGATGACCCTACATCCAGCTTCAGCAGCATCCCTGATGCTTTTT[G/A]GTGGGCTGTGGTAACCATGACTACAGTGGGCTATGGAGACATGCATCCAGTGACCATCGGAGGGAAGATTGTTGGCTCTTTGTGCGCCATCGCCGGTGTATTGACCATTGCGCTGCCCGTACCTGTCATTGTGTCCAATTTCAATTACTTTTACCACCGGGAGACCGATGGGGAAGAGCACGCACAATACCTGCACGTTGGCAGCTGTCAGCATCTCAACTCCACAGAAGATCTGAAACGGACACAAAGCACGTCCTCCCTCAGCAAATCGGAATATATGGTCATTGAGGAAGGAATAAATAGTGCTTTCAAACAGCCAAACTACTCCAACCAGAACAATCAAAACTGCGTGAATATTAAAAAGATTTTCACAGACGTGTAAATCGTGTACAGTGCCAGACAGTCGTACAATAATCACTACGATGATGGCACCTCTGCAAACGCAAGGTGCTGCGTTATTAGGGTACAGCGGGGCTAAAAGTCCTCCACAGCGGAGGACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33962

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

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109628	Nonsense	427	483	1	1

Genomic Location (Zv9):

Chromosome 6 (position 49309079)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	49368356
GRCz11	6	49367009

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGGAGACCGATGGGGAAGAGCACGCACAATACCTGCACGTTGGCAGCTGT[C/T]AGCATCTCAACTCCACAGAAGATCTGAAACGGACACAAAGCACGTCCTCC

Long Flanking Sequence:

ATTTCATCACTCTGGGGACGGAGCTGGCTGAAAGACAAGGCAACGGTCAACAAGCCATGTCGCTGGCCATCCTCCGAGTGATCCGTCTGGTGAGGGTCTTTCGCATCTTCAAGCTCTCACGTCACTCTAAAGGCCTGCAGATCCTTGGCCAGACTCTGAAAGCCAGCATGAGGGAACTGGGACTCCTCATCTTCTTCCTCTTCATTGGGGTCATCTTGTTTTCCAGCGCCGTCTACTTTGCTGAGGCGGATGACCCTACATCCAGCTTCAGCAGCATCCCTGATGCTTTTTGGTGGGCTGTGGTAACCATGACTACAGTGGGCTATGGAGACATGCATCCAGTGACCATCGGAGGGAAGATTGTTGGCTCTTTGTGCGCCATCGCCGGTGTATTGACCATTGCGCTGCCCGTACCTGTCATTGTGTCCAATTTCAATTACTTTTACCACCGGGAGACCGATGGGGAAGAGCACGCACAATACCTGCACGTTGGCAGCTGT[C/T]AGCATCTCAACTCCACAGAAGATCTGAAACGGACACAAAGCACGTCCTCCCTCAGCAAATCGGAATATATGGTCATTGAGGAAGGAATAAATAGTGCTTTCAAACAGCCAAACTACTCCAACCAGAACAATCAAAACTGCGTGAATATTAAAAAGATTTTCACAGACGTGTAAATCGTGTACAGTGCCAGACAGTCGTACAATAATCACTACGATGATGGCACCTCTGCAAACGCAAGGTGCTGCGTTATTAGGGTACAGCGGGGCTAAAAGTCCTCCACAGCGGAGGACAGTGTGATTTTATTGTTCCGGTCGCAAAATACGATATTTTTATGGAACATAGAAAGAGAAATATAATTTGTATAAAAGTAAATGTTAAAAGTAGCTTGGTTTAAATGAAAAAAACAACATAAACAAGGCAGCTAGGGGAAGAATTTGTCATCGTATATGCAAATACTTTTAATATAGCAAGATATTTTAGAGTAACATTTAAGTGTTTAC

Associated Phenotype:

Not determined