ZMP

LOC559036

Ensembl ID:

ENSDARG00000078650

Human Orthologue:

KCNA4

Human Description:

potassium voltage-gated channel, shaker-related subfamily, member 4 [Source:HGNC Symbol;Acc:6222]

Mouse Orthologue:

Kcna4

Mouse Description:

potassium voltage-gated channel, shaker-related subfamily, member 4 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14195	Nonsense	Available for shipment	Available now
sa20984	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa14195

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111055	Nonsense	34	497	1	1

Genomic Location (Zv9):

Chromosome 7 (position 33932282)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	32326622
GRCz11	7	32597772

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGAYGTCCTCAGTCAGGGTATGAAAACGTTTACAATGAGTACGGCTGCTG[C/A]GAGAGAGTTGTCMTCAACGTGTCGGGCTTAAAGTTTGAAACTCAGCTGAA

Long Flanking Sequence:

CGCGCAGCGGCCGCGGCAGCAGCTGAAGCTGGAGCGGTCGGAGAGGGAGGTGGGTCCACTGGCCATCCCCACAACCACCCGCATCAGAGTCGCGCCGCCTCTTCGACAAATGCCAACAACAGTAGCGCCGGGACCGCCTCGCGCCCCTCCTCCTCCTCCTCCTCACAACAGCCGCAACAGCAGCAGCAGCAGCAACACCACGAGCCACCACAGCAACTTCTCAGAGAGCGAAAAAAGCAAAGAGGCGTCGCGCGCTGGAGACGGAACCGCGCGGCTCTCGGCGGGGATCTACGCCAATCAGAGTTGGCGCTCCTAGGATCCGAGGAGGACATTATGATCGAGGAGGAGGAGGAGGCGGAGGGCGAGGAGGAAGAGGAGGACAGGAAAAGCAAGAGGTCCAGTTTTGTCTATAACATGGATGATGAGGAGGAGACGGTGTCGTTAACGGACAGACGTCCTCAGTCAGGGTATGAAAACGTTTACAATGAGTACGGCTGCTG[C/A]GAGAGAGTTGTCATCAACGTGTCGGGCTTAAAGTTTGAAACTCAGCTGAAGACTCTCGCGCAGTTCCCGGACACTCTCCTGGGAGACCCCGAGAAAAGAAGCAGGTACTTCGACCCTTTGCGTAACGAATACTTCTTTGACAGAAACCGACCGAGCTTCGACGCCATTCTGTACTTCTATCAGTCAGGGGGGCGCTTAAAGAGACCCGTCAATGTGCCGTTTGACATCTTTTCCGAGGAGGTCAAGTTCTATGAACTCGGGGATGAGGCAATGCTCAAGTTCCGCGAGGATGAGGGCTTTGTGAAGGAGGAGGAGAAGCCGCTGCCCGAGGACGAGTTCAAGCGTCAGATCTGGCTGCTCTTCGAGTACCCGGAGAGTTCAAGTCCAGCCAGAGGGATCGCGGTCGTGTCAGTGCTGGTCATCGTCATATCCATAGTCATTTTTTGTTTAGAAACATTGCCAGAATTCAGGGACGACAAAGAATTCCTCATCCCAGGTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20984

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111055	Nonsense	194	497	1	1

Genomic Location (Zv9):

Chromosome 7 (position 33931804)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	32326144
GRCz11	7	32597294

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATCCATAGTCATTTTTTGTTTAGAAACATTGCCAGAATTCAGGGACGAC[A/T]AAGAATTCCTCATCCCAGGTAAAAACTCCACGCAGGCAGACAATGGATTT

Long Flanking Sequence:

TTTACAATGAGTACGGCTGCTGCGAGAGAGTTGTCATCAACGTGTCGGGCTTAAAGTTTGAAACTCAGCTGAAGACTCTCGCGCAGTTCCCGGACACTCTCCTGGGAGACCCCGAGAAAAGAAGCAGGTACTTCGACCCTTTGCGTAACGAATACTTCTTTGACAGAAACCGACCGAGCTTCGACGCCATTCTGTACTTCTATCAGTCAGGGGGGCGCTTAAAGAGACCCGTCAATGTGCCGTTTGACATCTTTTCCGAGGAGGTCAAGTTCTATGAACTCGGGGATGAGGCAATGCTCAAGTTCCGCGAGGATGAGGGCTTTGTGAAGGAGGAGGAGAAGCCGCTGCCCGAGGACGAGTTCAAGCGTCAGATCTGGCTGCTCTTCGAGTACCCGGAGAGTTCAAGTCCAGCCAGAGGGATCGCGGTCGTGTCAGTGCTGGTCATCGTCATATCCATAGTCATTTTTTGTTTAGAAACATTGCCAGAATTCAGGGACGAC[A/T]AAGAATTCCTCATCCCAGGTAAAAACTCCACGCAGGCAGACAATGGATTTACGCCATTCAACGACCCCTTTTTCATCGTGGAGACAGTGTGCATCATCTGGTTCTCGTTTGAGATCATCGTGCGCTTCTTCGCCAGCCCCAGTAAAGCTGATTTCTTTAAAAACGTTATGAACACCATAGACATCGTCTCTATTTTGCCTTATTTCATAACCCTGGGCACAGATCTCGCACAGCAGCAAGGCAACGGGCAACAGGCTATGAGTTTCGCCATCCTGAGAATAATACGACTCGTCCGGGTGTTCAGGATCTTCAAACTGTCTCGGCACTCCAAAGGTCTCCAGATCCTCGGGCACACTTTACGCGCGAGCATGCGAGAGCTGGCGCTGCTCATCTTCTTCCTCGTCATCGGCGTCATCCTGTTCTCCAGCGCGGTGTACTTCGCAGAGGCGGACGAGCCCACGTCACAGTTCACCAGCATCCCAGATGCGTTTTGGTGGGCT

Associated Phenotype:

Not determined