ZMP

zgc:174907

Ensembl ID:

ENSDARG00000091458

ZFIN ID:

ZDB-GENE-080204-89

Description:

potassium voltage-gated channel subfamily A member 2 [Source:RefSeq peptide;Acc:NP_001104640]

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 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39393	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa7308	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39393

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000121427	Essential Splice Site	None	495	1	3

Genomic Location (Zv9):

Chromosome 23 (position 5105073)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	5096569
GRCz11	23	5032465

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTTAATTTGTGTGCAGTTTGCTCCCACCATACATCTCCACCTAACTCAG[G/A]TTAGTCACTCATGTTCTTGGCTGTAGTGAGTCTCCTTACGTGGCTATTCA

Long Flanking Sequence:

GGAGCCACATGTTTGTTAGTTGTTTTAGCCATTGGCCTTTATTTAATTCCCCGCAGACCATGATTTCAGATTAAAAATCATCTGAACTAAAACATGTGCATCTTGGATGTCATAACGGTAAGTAAAGTTACTTTTATTAATATATTAACTTAGAAAATTTTATTTTCCTGAAGTATGCTCAAATTCATAGTCACACTGTCTAGGGAATGTAGACCTGACTACAGCTGATGATGCTTGAGCGCTCGGTCTCTATGGCTGTCAGGTTGTGGCCACAGATGGGCTGGATTGTCACCATGTTGGTGAGGGAGTTGAAGGGAAATGCTGTCACACTGTGACCAGATGGAGTCACTCTATCTCTGGCTTGTGTAGTAGGTGTTTACTTTTTATTGACTAGCTTCTAATAACCCAGTGAACCTACGTTTGCTGTCATCTGTTGTTTGGTTACATAATTGTTAATTTGTGTGCAGTTTGCTCCCACCATACATCTCCACCTAACTCAG[G/A]TTAGTCACTCATGTTCTTGGCTGTAGTGAGTCTCCTTACGTGGCTATTCATTCCACTGGGTCTGAATACTCACACCTGCTCCCGTAACACACTCCATTTATCATCACCACACACACACACACTCCTATAAATCTCATTATGGAGTCATAGCTGACTCAAAGCAGATGGTCTTCCTCATGTTTGTCCCAGACTGCTGGCTTTTTCCACACCAGAATGCCGTTCTAGAGAGATCTTTCCAGGATCCTACCGAGAAACTGTCTGCTGAAATGGGAACAGATTATATTCCAGCAGAAGGGGTTTTCCTTTGTCCTTCAAGCTTGGCTTTCTACCTTTTTTGCATAGCCCATCTTAAAGAAATCCCCTGAGGTCTTTTTAAGAGGAGACAGTCTTCATGGCCCATATTCAGTTTAGTTAAATTCAAGTTTGTTTGTATTGTGTTTTTTTAATTAATTATTTAACAATAATTGTTTCAAAGCAGCTTAAAAAAAAAGAAAAGATGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7308

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000121427	Nonsense	154	495	2	3

Genomic Location (Zv9):

Chromosome 23 (position 5127623)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	5076380
GRCz11	23	5012276

KASP Assay ID:

554-4759.1 (used for ordering genotyping assays)

KASP Sequence:

AGAAACTACTGCCAGAGAATGAGTTTCAGAGGCAGGTATGGCTGCTTTTT[G/T]AGTACCCTGAAAGTTCAGGGCCTGCCCGGATTATTGCTATAATTTCAGTC

Long Flanking Sequence:

TGCATCCTGACCCTAAACTGCAGGTTGCCTTCATTCACAGCATGACTGTTGCCACGGGTGACCCAGCCGATGAAGCCGCAGCTCTCCCGGGTCAGCCACAGGACACATATGACCCGGAACCAGACCATGAGTGCTGCGAAAGGGTGGTCATTAACATCTCTGGTCTGCGCTTTGAGACGCAGCTCAAAACTCTGTCTCAGTTCCCAGAGACATTGCTTGGAGACCCTAAAAAGAGAATGCGCTACTTCGACCCTCTGAGAAATGAGTACTTTTTTGACAGGAACCGCCCAAGTTTTGATGCCATTCTCTATTACTACCAGTCAGGCGGCAGGCTCCGGAGGCCTGTCAATGTGACACTGGATATTTTTTCAGAGGAGATACGTTTTTATGAGCTTGGGGAAGAAGCCATTGAGATGTTCAGGGAGGATGAAGGATTTATTAAGGAAGAGGAGAAACTACTGCCAGAGAATGAGTTTCAGAGGCAGGTATGGCTGCTTTTT[G/T]AGTACCCTGAAAGTTCAGGGCCTGCCCGGATTATTGCTATAATTTCAGTCATGGTTATTCTCATATCCATAGTCAGTTTTTGCCTGGAGACACTTCCAGTTTTTCGCAATGAAGAAACGGATATGCACAAAGCATACAGAACCGACTCCAACTCAACAATTAGCTATACTTCCACTTACTTTACTGACCCTTTCTTCATCTTGGAGACACTTTGCATCATATGGTTTTCCTTTGAGTTCCTGGTGAGATTCTTTGCATGTCCAAGCAAAGCAGGCTTCTTTGTCAATATAATGAACATCATTGATATTGTGGCTATAATACCTTACTTTATCACCTTGGGAACAGAGCTTGCAGAGAAAGCTGAAGATGGTCAGCAAGGTCAACAAGCCATGTCTCTTGCCATCTTGAGGGTCATCAGATTAGTGCGAGTCTTCAGGATCTTCAAACTTTCCCGGCATTCAAAAGGGCTGCAGATTCTTGGCCAAACACTCAAGGCCAGC

Associated Phenotype:

Not determined