ZMP

LOC100330283

Ensembl ID:

ENSDARG00000063282

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 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37608	Nonsense	Mutation detected in F1 DNA	Not yet available
sa3232	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa37608

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092321	Nonsense	65	482	1	1

Genomic Location (Zv9):

Chromosome 23 (position 5077672)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	5123970
GRCz11	23	5059866

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCAAAACCCTGTCCCAGTTCCCCGAGACGTTGCTTGGAGACCCCAAGAAA[C/T]GAATGCGCTACTTTGACCCACTCAGAAACGAATATTTCTTTGACAGGAAT

Long Flanking Sequence:

TTTAGATGTGTGATGAGCATCCGCGCGCCGTGGGGCGGGAGCAGCCGTGTTTATAAACCACAGTACGCGCGTCGTGGGCGGGAAGACTGGATTGAGAAAGTAGTGATTCGAGAAAGAGAGGAGTACGCGCGGCAGCGGCGGGCGGCTGTGGCTGACTGGAGATCGTGGAGGAGGCGCGGCTTCCACTGCCCCTCCACTTTAACAGCTGTATGGACGACCACCTCAGCCTCCTCCACTCGCCTCCACCTTTCTCGAGCAAGCACCGGGGCAACAATCTCGTGAACCACGGCTACACAGAAAACGACACTATGACAATTGTTGCATGCGACAACATGCTGGAGGAGTCGGCGGCACTGCCCGGGCACCACTCTCTGGAGCGCTACGAGCCCGACCATGAGTGTTGCGAGAGAGTTGTCATCAACATCTCGGGCTTGAGGTTCGAGACGCAGCTCAAAACCCTGTCCCAGTTCCCCGAGACGTTGCTTGGAGACCCCAAGAAA[C/T]GAATGCGCTACTTTGACCCACTCAGAAACGAATATTTCTTTGACAGGAATCGCCCGAGCTTCGATGCCATTTTATATTACTACCAGTCAGGGGGTCGTATTCGGAGACCAGTAAATGTCCCTATTGACATTTTCTCCGAGGAGATTCGCTTCTATGAGCTCGGGGAGGAAGCCATGGAGAAATTCAGAGAGGATGAGGGCTTCATAAAAGAGGAAGAGCGCCCTTTGCCCACCAACGAGTTTCAGCGACAGGTGTGGTTGCTGTTTGAGTACCCGGAGAGCTCGGGTCCTGCCAGGGGCATCGCGATCGTCTCCGTGCTGGTCATTTTGATATCAATCGTTATCTTTTGCCTGGAAACGTTACCCGAGTTTCGGGACGACATTGACTCGACGGTCGCGCCGGTTGTAAACGGAACTATCCCGTATCTCACGAGCCCCTTCTCCGACCCGTTCTTTGTGGTCGAGACCCTGTGCATCATCTGGTTCTCGTTTGAGCTGCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa3232

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092321	Nonsense	100	482	1	1

Genomic Location (Zv9):

Chromosome 23 (position 5077777)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	5123865
GRCz11	23	5059761

KASP Assay ID:

554-3199.1 (used for ordering genotyping assays)

KASP Sequence:

CGAGCTTCGATGCCATTTTATATTACTACCAGTCAGGGGGTCGTATTCGG[A/T]GACCAGTAAATRTCCCTATTGACATTTTCTCCGAGGAGATTCGCTTCTAT

Long Flanking Sequence:

ATTCGAGAAAGAGAGGAGTACGCGCGGCAGCGGCGGGCGGCTGTGGCTGACTGGAGATCGTGGAGGAGGCGCGGCTTCCACTGCCCCTCCACTTTAACAGCTGTATGGACGACCACCTCAGCCTCCTCCACTCGCCTCCACCTTTCTCGAGCAAGCACCGGGGCAACAATCTCGTGAACCACGGCTACACAGAAAACGACACTATGACAATTGTTGCATGCGACAACATGCTGGAGGAGTCGGCGGCACTGCCCGGGCACCACTCTCTGGAGCGCTACGAGCCCGACCATGAGTGTTGCGAGAGAGTTGTCATCAACATCTCGGGCTTGAGGTTCGAGACGCAGCTCAAAACCCTGTCCCAGTTCCCCGAGACGTTGCTTGGAGACCCCAAGAAACGAATGCGCTACTTTGACCCACTCAGAAACGAATATTTCTTTGACAGGAATCGCCCGAGCTTCGATGCCATTTTATATTACTACCAGTCAGGGGGTCGTATTCGG[A/T]GACCAGTAAATGTCCCTATTGACATTTTCTCCGAGGAGATTCGCTTCTATGAGCTCGGGGAGGAAGCCATGGAGAAATTCAGAGAGGATGAGGGCTTCATAAAAGAGGAAGAGCGCCCTTTGCCCACCAACGAGTTTCAGCGACAGGTGTGGTTGCTGTTTGAGTACCCGGAGAGCTCGGGTCCTGCCAGGGGCATCGCGATCGTCTCCGTGCTGGTCATTTTGATATCAATCGTTATCTTTTGCCTGGAAACGTTACCCGAGTTTCGGGACGACATTGACTCGACGGTCGCGCCGGTTGTAAACGGAACTATCCCGTATCTCACGAGCCCCTTCTCCGACCCGTTCTTTGTGGTCGAGACCCTGTGCATCATCTGGTTCTCGTTTGAGCTGCTGGTCCGGTTCTTCGCGTGCCCTAGCAAAGCCACGTTCTCGAAGAACATCATGAACATTATTGACATCGTTGCTATTATACCATACTTCATCACTTTGGGCACCGAG

Associated Phenotype:

Not determined