ZMP

kcnab2

Ensembl ID:

ENSDARG00000087247

Human Orthologue:

KCNAB2

Human Description:

potassium voltage-gated channel, shaker-related subfamily, beta member 2 [Source:HGNC Symbol;Acc:622

Mouse Orthologue:

Kcnab2

Mouse Description:

potassium voltage-gated channel, shaker-related subfamily, beta member 2 Gene [Source:MGI Symbol;Acc

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41909	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa44747	Nonsense	Mutation detected in F1 DNA	Not yet available
sa21974	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa41909

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
ENSDART00000127292	Essential Splice Site	94	367	6	15

Genomic Location (Zv9):

Chromosome 11 (position 42748395)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	41038890
GRCz11	11	41651120

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTCAGTAAGATGACCGATTAGTCTGATAAGCATCTGGTTTTGTGTTGCA[G/A]GGCGGAGGTGGTGCTGGGCAACGTCATAAAGAAGAAAGGATGGAGGTATG

Long Flanking Sequence:

ACATGACAGTCAAAGCAGAATTAAATAGCTTAATAAATAATAGTAAGATTAAAATATATATACATAAATGAATGGTCGAGGTTGTGGAGGAATATAGGTACCTAGAAACAATTATTGAATGCAAATTGAATTTTGACCAAAACACATGCAATTCCATCAACATCAAAGGCTGTTTTTCTTGCGTAAACTCTCCTCTTTTAATGTAGAGAGCAAAGTGCTGTGCAGAAAATATACAGCAAAATAAGCATAATAATATATAAAATAGGCGAAGCAGTGGCAGATAAATGGGCATAATAGGTCTCCTTTAAATATGAAAATACTGGTATGTTTTGAAATAAAATGTTTTGATAGAGTCTTGCCCGTGGATTGTGTTTTTAATTTACATGAATGCATCGTATCACATTGCTGTCTTGGTTTACTCCCACCGGTGGCCCATTCTGTTGTCGTAGATGTCAGTAAGATGACCGATTAGTCTGATAAGCATCTGGTTTTGTGTTGCA[G/A]GGCGGAGGTGGTGCTGGGCAACGTCATAAAGAAGAAAGGATGGAGGTATGTTCACCAACAGCATACAGCTTTTCATTTCCTCTTCTTATCTTGTGCTGATAGCTCGGCCCAGTGCCTCAGAGATTGTGTCACCGCAACCCCAGACAGGCACAAATATAAATTATTAAAGCCTGGCTCGCCCTGTTGATGTGCCATCTAGATATTGAATTATGAAAGAGTCGCATATGTGTGTGTTTGTCGTGAAGCCGATGTCCTGATAAATGTGCGTGACAGAAGTTCATGGTTGATAGAAGCACTTTTTAGGATGTATTAAAGGGATATTTCACTCAAAACTTAAAATTATGGCAATATTTACCTACCTTGAGTTTCTTTCTACTGGGGATATTTTGAATAATGCCATTGACTGCCATTGTATGTTTATTTTTCCTACAGTGCTATGGTTTTCATTAGCTGTTTCCAACTACCTTCCTACTTTTAGAATATCATTTTGAAATATCATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44747

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
ENSDART00000127292	Nonsense	204	367	11	15

Genomic Location (Zv9):

Chromosome 11 (position 42766489)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	41056984
GRCz11	11	41669214

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTCTATTATTTTGTCCATGTGTTGTAGGAAGCATATTCAGTGGCCCGA[C/T]AGTTCAACCAGATCCCACCAATCTGTGAGCAGTCGGAGTATCACATGTTC

Long Flanking Sequence:

AGGCGGCATGGTGGCTTAGTAGTTAGCACTTGCCTCACAGCAAGAAGGACGCTGGTTCAAACCCCGGCTCGACCAGTTAGTGTTTCTGCGTAGAGTTTGCTTGGTCTGACTGAATTAGGTTTGGGTCGATAGACAATGCCATCACTGACGTTTCATCTAGCATTTATGAAAAGATCTACGTCCACACTATACCGCTGAAAACGCACATCACCACACACACACACACACACACATACTCTGCGGTGTAAGCGCACGTCTGAGCTCCAACAGTCAGCAGTTGCTTTGAGCACAAAACCTCAGAGAGCAGTGCACGTCTAACAATTTATCAAGGATGTACCACTGGATGGCGTTTCACTGTAGTTGTTAGACGTGATGTTTAATTAATCTTGTCTTTATCTAACCACTCTTCGGTCTTCTGAATCTGTCAGTGTCACAGCATAGTTTTCCTCTAACTCTATTATTTTGTCCATGTGTTGTAGGAAGCATATTCAGTGGCCCGA[C/T]AGTTCAACCAGATCCCACCAATCTGTGAGCAGTCGGAGTATCACATGTTCCAGAGAGAGAAAGTGGAGGTGCAGCTCCCTGAGCTCTTCCATAAGATCGGTGAGCGTCCAGTCCACCAAAACCCTCACCAGACCTCAACAAACATTTTGCTTCAACTCAAGCTGTTTGTATTACTATAGGGCATTATAGGGTAACTTATTAGGGCAATGGGTTACAGTTACAATATTTTTGCCTATTCGAAATACGAAAATAGCCAAGAAATATCGCTCTGCAAAATTGCCTGGCTACATTGCTCAAAAAGTTGAAAAAAGTAAATCAGTTGCAAAAAGTAAAATCAGCATTATTCTCCAACCCGGGCTCATTGTGGAAACGTAGCCCCGCGGACATTTCTGCAGACCGCGATTTACGTCCCGGGAGGTACGTTTTCGAGCGGTTTTTGTTTTCGCGGATCCACGAGAGGTTGCTGTGCGCGCTTTTTCGCTGCTCGGGCGCCTCTCGGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa21974

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
ENSDART00000127292	Nonsense	283	367	13	15

Genomic Location (Zv9):

Chromosome 11 (position 42783386)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	41073881
GRCz11	11	41686111

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTAACAGGGCTACCAGTGGTTGAAGGACAAGATCTTGAGCGAGGAGGGC[C/T]GACGCCAGCAGGCGAAGCTGAAAGAGCTGCAGGCAATCGCTGAGCGGCTG

Long Flanking Sequence:

ACTTTTCGCATAGACAGTCAAAATAGAGCTCGTAAAGTGAATGGGAGATGAGACTCTGATTGGTTTAAAGCATGTTATGCTCAAAACACACCTATAACTCATTAAGAGAATAAGCACAACCCTGTTAGACCATGCACCGGGTGCAGAGTGTATTTTTCCATCCTTAAAATAGCAAAAGTGGATTCGGACTTACTCTTTTTGCGCCATGAGCTTTAGACTTTGCTCCTAGATCATTAAAATAGAGCCCTTAGAGTGTAGAATTTCAAGTCAGCAGCACCTCTAGAATTTAGCATTTTAAGTCAGCAGGCTTTGATTTCTGATAAAAATGGTGACGTGTTCAACCTTCTTTCCTCCCACTGTACTGTACCGTATGTGTTGATGTGTGTGTGTGTGTGTGTAAATGCACCGCTGTAGGCGGGGGCCGCTGTTTTTGAGCAGGTGTGCTGTGTTGTTAACAGGGCTACCAGTGGTTGAAGGACAAGATCTTGAGCGAGGAGGGC[C/T]GACGCCAGCAGGCGAAGCTGAAAGAGCTGCAGGCAATCGCTGAGCGGCTGGGCTGCACACTGCCACAGCTAGCCATCGGTACGCCAAACACCCAGAGACACACTGCCGCTCTCTCTCTTTCTGTCTGTCTGTCCGTCCGTCCTGTTCCTCGCTCATCCTCTCCCTCTCATCTTACCCTTAATTCCTCAGACCAGGAGCTGACCGCAAATACCATTAGCTCGTGGCGTTAATGGAAGACGGTTCCTGCCTGCAGATAATAGCTTAATGTCTATCTGGTCTAGTGTTTTCTGATGCTCTATATGGGACGTGTTGGGGGGTGCTTTAAGGAGAGAATGGAGAAATTGTTAAGGGAACATCAAACTAGTTCCAAATCTTAATGTAACAGAAATGCTAAAATGATCTTAAAAGCAAATAATGCAAAGATGTTTTAATTATTATTTTATACATATATATTTTTTAATTATTTTTATGTTTATTTTATCTTAATTTTTGAATGATCT

Associated Phenotype:

Not determined