Busch Lab

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 are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa32858 Nonsense Mutation detected in F1 DNA Not yet available
sa16058 Nonsense Available for shipment Available now
sa9113 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa32858
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
ENSDART00000110337 Nonsense 9 898 1 21
Genomic Location (Zv9):
Chromosome 2 (position 11853408)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 12278504
GRCz11 2 12062103
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGCATTTGTTTCTAACTCTCCAGCATTTGTGGTGTTGAGCACTTGCAG[C/T]GAGCCGGAACAAAACTCACAGTTTTTGACTCTTTCTACTTCTGCATCGTG
Long Flanking Sequence:
TGGGTCATTTGGTGTTTTTAAAAACAGTATAGCCTATAGGTTGGGTTTAGAGAAGGCGGAGGATGGGTCAGTCAGTCAACAGCAGCCCTTTGGAGGTTTTACATGAGAACAGTACGCCTGAATGGCACTCACAAGAGAAATTTGAGATCTCAAAAAGCATACACAGGGGCCTCTGGTGGATTTGTGAAAACAAAAACTTGAAAATAAAACATATTTTACGCTCTCCAGAAATGTACATAGTGGTACATTTTCAGAATGAGCATGGGTTGACAATAATATATAAAAAATAATTTTAAAATGAAATAAAAAATACACAAACGTTTAGCAATGAAAATGAAATAAATAGAGCCCAATTTCTGCATAGGAGAAGCATTTTAAGTCTTTTGCATATTGTATATGGCATCACTGTTCTGCAAAACTACCATGGACTTCTTTGTGATGTTTGCTTTTGTTGCATTTGTTTCTAACTCTCCAGCATTTGTGGTGTTGAGCACTTGCAG[C/T]GAGCCGGAACAAAACTCACAGTTTTTGACTCTTTCTACTTCTGCATCGTGACCTTTTCTACAGTGGGGTTTGGAGATGTTGTTCCTGATATTTGGCCATCCAAGTTGCTGGTGGTTTTTATGATACTTGTCACTTTAATGGTCCTGCCAATCCAGGTAAGCCTGCTTTTGAGAATACCGAGTATGCAGTTAATAATGCAAGGTCCCACTTTATATTAATGATGCTATATAGTGCATTGATTTTTGATATCTACATAGTAGGTATGTGGCTTGGGTAGGTTAAAAAATGTATATGGTCATTCATAAATAGAGGAGTTACCCCTTGAATTATCTTCATAAAGACCATATTTGGAATGGTTATGATTAATAATGAGCTCAGCTCTGTCACTCCTGCAGCTCAGTCCCTGCTCTCTATCTCACTCAAAAGCAAACATAATGATGTATTTTTAAATAAACTGTGAAAAAAAAATCATTACGTTTGTCAAAATCTTTAAACAAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16058
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
Order Allele From EZRC
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

Mutation Details

Allele Name:
sa9113
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110337 Nonsense 797 898 19 21
Genomic Location (Zv9):
Chromosome 2 (position 11819091)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 12244187
GRCz11 2 12027786
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTAGATGAGCAACATCAGARTCTTCAATGYGAAATACCAGACAGTCAAT[T/A]GCAGACACAGTCTCTGCGTCGGAGAAGCATGCAGTGGGCTTCCAGTCTCC
Long Flanking Sequence:
CTAGTTTTGGCCTATTTTTAGACGTTTTTCAGCCTAAGTTTGGCCCTTGTTTTAGCATAGATAACTATGTTTAGATGTCTATTAGACATCTTTTAAAAACAAAAAATTCTTGCTGGGTAGCTTTGTGTTAATGATTTTATTTTATGTTTTTTCAGTGGTCTTAAAATCTGAAATTACGTTTCAGATGAGCATCACCGAGGAGGACCTATGCATTGAGACATATGGCAGGCTGTACCAAAGGCTTTCCTCCACTGTAGGAGATATTCCCATCGGCATCTACAGGACCAAGTCTCAAACAGTTGAATCCCCTGAGGTAGCATTGTCCATCTGAGATGGCTTTAACAACAGTTTTGTAAGTGTTCTGTGGATAAAGAGGCTATGTTTTTCTTTCATCAAGACTCCACAATTCCAAATGTCAGACAAGGCATCTGTGTTTGATGAGGGCGGAGACCTAGATGAGCAACATCAGAATCTTCAATGCGAAATACCAGACAGTCAAT[T/A]GCAGACACAGTCTCTGCGTCGGAGAAGCATGCAGTGGGCTTCCAGTCTCCTTGGGCCATGGCACACTGAGCGTGAGGCAGACAGATTGAGTCAGCATCGGGGTGTCCTGCTTTCATGCTCTGAGAGACTGGAGGTCACAGAGCTGGTCAAGAAACGCATGAAAAACCTGGGCCTATCCACTCTGGGATTTGGTAAGATTCAAGTCAAATCATGTTCAGTACGAACTAGGAAGACTCTAAGAATTGTCTGAAATTAATTTTTTTATCAATTATTTTATTTGATTTTAAGAACTCTAGAACCAGGCTTGACTGTTAATATTTGTTATATTAATATTTGTTATATTGTATTAGTTTGGGGACTTCAAAAAACATATCTAAGTTAATGAGATAATTATGCACCTTCACCACGCACACACCCTGTGCAGCAACAGGGCATGGCCAGAGGCGCTGTAATTTTATAGCAGAGAAAGCTAAAATGTAGTTAAATGCTGCTAATTCCAC
Associated Phenotype:
Not determined