ZMP

LOC568327

Ensembl ID:

ENSDARG00000075812

Human Orthologue:

KCNT2

Human Description:

potassium channel, subfamily T, member 2 [Source:HGNC Symbol;Acc:18866]

Mouse Orthologue:

Kcnt2

Mouse Description:

potassium channel, subfamily T, member 2 Gene [Source:MGI Symbol;Acc:MGI:3036273]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa16058	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa16058

Status:

Available for shipment
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Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110337	Nonsense	538	898	12	21

Genomic Location (Zv9):

Chromosome 2 (position 11831315)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	12256411
GRCz11	2	12040010

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GAAACAGCCTGTACAACTTCATCCTCCCATTACGAGCCTCGTAYAGACCA[C/T]AGAATGAACTGYGGCCCATTGTGCTGCTCTTGGAGYATGTGTAAACATCA

Long Flanking Sequence:

ATAAGAGTAAAGAGTCTTTCTACAGGAAGGGGGAGGTTTTTTTTTTTAATGAAGATAAGAGTAAAGAGTCTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGAAGCACACTTTATAAATATTGAGGATTTTTGTCTGTTGCAAATGTGCAAAACCAGTGCATGTGTCAGTTAAATTATTAGAGAGATGAAAAAGTGTGTTTTATACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGAGCCACACTCACTTTGAGGTTTTACAGGTGATAGAGGAAGAGATTTCTAGTTTTTAGTTGTTTTAGTAATTGTTTGAATGATAATGAGACTAATCTTCTTCTTGTAATGTCAGTTTTTGTCCAAGACCTGCAACCACAAAGACGATGAAGATGCAAAAGTGTATAGTTTGAAGAGTAAGCTGGTCATTGTGTCTGTTGAGACAGCAGGAAACAGCCTGTACAACTTCATCCTCCCATTACGAGCCTCGTACAGACCA[C/T]AGAATGAACTGTGGCCCATTGTGCTGCTCTTGGAGCATGTGTAAACATCATTTTTACACAACTCTTCTTCACTTTCTACTGTTTTGTAGTCATGAAGAGTGCTACAATGTCATGTTTCTGTGTGGTTTCTTTGTCTTTTAGACCGGATGAAGAATTTCTTGAGACGATCAGTTGGTTTCCAATGATTTACTACTTGCTTGGATCAATCGACAGGCAAGAGACGTTATTATGAAACATTATCATGTTTGCTTGTATCCTGGCCTCGAATAATCAATTTGCAGTTGGTCCTCCGGAAGGAAATAAGCCTGCTGCTGTGCACCGAGAGTCACCTTACTGAGATCAAAGCTCAAAGAACGAGTCTAACTGTAAAATCAGGGAACAAATAAGCAACTTTGATAAAAACAAGCATAAGAACACACTGCAAATAAATACTTTTCTTGATTCTAGTTATCTAAAAAAATCTTAAATCAAAAAGAATTTTTGTGACAAGCAAAAAAAAA

Associated Phenotype:

Not determined