Busch Lab

ZMP

LOC565691

Ensembl ID:
ENSDARG00000074551
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa25260 Nonsense Mutation detected in F1 DNA Not yet available
sa11833 Nonsense Available for shipment Available now
sa26142 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25260
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110065 Nonsense 781 1195 24 33
Genomic Location (Zv9):
Chromosome 3 (position 48115900)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 50117040
GRCz11 3 46927680
KASP Assay ID:
554-7766.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCTTTCTTTCACTAGACCTGAGGCAGACTTCTTGGAGGCCATCTGCTG[G/A]TTTCCTATGGTCTTTTACACAGTGGGCTCCATTGACAAGTAAGACTAGTT
Long Flanking Sequence:
GGCTGAATGGCTAAATGGTAAAAAAAATGGCTAGAATTGGTAAATCTCAACTGTTTAACTGCATGGGAGTTGTAAAATAAGCAGTTTTACTCATGGCAAAAAAAATAAATGGAGTACTTTAAACAACATCCATTTTGTTTTTCACAGTGCTGACCACTTTTCTGTATCTATCATGATATGCAATCATCGTTTCTGCTGTAACCGAAAACTAATATGGAGAGATTCACCATCATGTAATGCAATCAAATGCAATAAAACTCTTGAGTCATCTTGTTTTTTTCCCTTAGCAGATGTGCAGCTGCAGGCTGAATTAAATTATTTAGATGCCCTAGAGCAGTGAAGCTGTGAGATTTTTATAGACATTGGGATGGTTTCGTACAAATACCTGGAAAAAGACATTCATGATTCAGTTTGCAGCTTTGGTCAAGGCATCACCTCAGATTTTTAACATGCCTTTCTTTCACTAGACCTGAGGCAGACTTCTTGGAGGCCATCTGCTG[G/A]TTTCCTATGGTCTTTTACACAGTGGGCTCCATTGACAAGTAAGACTAGTTTTACTTTAAGCTTGTATAATCTCAAACCTAAAATTTTTCAGACACATTCAGCATCTCATAGTTTAGAAAATGGTAATGCAATATGACACAAACTCAGAGTTAAACTCTGAATAAATACGACCCTGGATCATAAAACCAGCCTTATTTTGCACTAAATGGGTAAATTTTTGCAAATAGCCACTGCTTTTTAGTCATTTTGTCATTTTTTGACACCTCAACCTTGTGCTTTCAGTCTGGATAGTCTTTTGCGTTGTGGTGTGACATTTGCTGACACCATGGTAGTTGTGGACAAAGAGAGCTCTATGATTGCAGAGGAGGACTACATGGCTGATGCCAAGACCATTGTTAATGTTCAGACACTCTTCAGGTAGGTTTATCCACATGAATCTTTTTAATGAAGGCGTTTTTGGGCCTTGACACCCCTTTCCTCACTGTTTCTCAAAGGCTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11833
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
ENSDART00000110065 Nonsense 1051 1195 30 33
Genomic Location (Zv9):
Chromosome 3 (position 48111696)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 50112836
GRCz11 3 46923476
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCCATGGAYCACCCTYTACTGAGGAGGAAGAGCATGCAGTGGGCACGA[C/T]GACTRAGTCGTAAGAGTGGACGAGGATCCGGCGGGGCGAAGGGAGTGGGG
Long Flanking Sequence:
ACTATTCTAGACTTCTAGACTAATCCATATGGTAACTCTGTGCTTAGGTATGTGATGTAACCTCCAGCTGGGGTGGGTTTCTGGGACCTGCTTAAAATGTTTATGCAATAATGAAATACATCTGTTTGATCTTCCTCTATTCTTTACAGTAACTTAATTTCTTAATGTTTTCCCAACACAAATCAATTGTGTGGATGCCAGCATTTTTACAATGAATGGTGGTCTCCAATGAGTATATATTTTAAAAAAGTATTCAAATATTTTACTTTCTAACAATTCCACATTATTTTCAAATAAATGCTCCATTGTGTGGCTTGTCTCAGTCTCAGGTGTCCATCACGGTGGAAGACTATGAGGATACACGCGAGCCCCGTGAGCCTCTGCTCTGCCGCTCCGGTCTTCATCGCAACTCAACGTCATCAGAGCCGCCCTCCTCCTCCTCATCCTCACAAGCCATGGACCACCCTCTACTGAGGAGGAAGAGCATGCAGTGGGCACGA[C/T]GACTAAGTCGTAAGAGTGGACGAGGATCCGGCGGGGCGAAGGGAGTGGGGAGCGCAGCTGAGCGCATCACCCAGCAGAGGCTCAGCCTGTTTCGCCGCTCCGAGAGGCAAGAGCTCAATGCTTTGGTCCGCACACGCATGAAGCACCTGGGGCTCTCACCATCTGGATTCAGTGAGTGTAAATTTGAATTTTGACTTTATTCACCAGCATGGACCATGCCACACTTTGGGCTAGACTGTAATGTAGAGATGAAGGGAGAAAAAAGGGTTAGGGGAATACTGAACAGGAAGGTAGGTCGATCGGGTGTCCTACGATGATGCTGAGAGACTAAGAGTGGGATTATCATCTCTGAAATGTAGTATAATAAATAAGGTTTAATAGAATGATTTGGACCTTCCAATTTAACCTAGGAGGGAAGAGAGGGCTATAAGGACTGTTAATGGGAAGCAAGGAATCCTGGTCTGCCTTAAGTAAGTTTTAGAGAGTAGGTGATTGGTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26142
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110065 Essential Splice Site 1127 1195 32 33
Genomic Location (Zv9):
Chromosome 3 (position 48108951)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 50110091
GRCz11 3 46920731
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTAGAGATATTAAGTTGGTCTAAATTATAGTTTTGTACCCTCTGCTTA[T/A]GTCAGATGGGATGACAGACCAGGGCAACAGACTGTCCTATATTCTTATCA
Long Flanking Sequence:
AGTAGGCATACCAAAAATGCGAAAGTTAGCACTGAATCCCTTAGGTGTTTTTATTTTTATACTTTAGTTTGCTAGCTTTGCATAACCTCCACATATTTTTATCATTCTTTTCCGTGATATACAACCAATTGTTTTCTAGATTAGAGCTTCTTCACAATGTCATCAGTAGCTATAAATTGCACAAGCCCTTTATATTTAAATGGCTTCTTACTGTCTAACAGTATTTTAACGTTTAGCTAAGAAATAAAAGTCACTGTATGATATAGTTTCTCTACGTGTTTGTTGTTATTGTTGTGTTCTGAATTTTGCTGTAGTTTTACATTCAGAACTATAGATTTAGAACTATATTGTTTTCATTATCATGCTTTGTGTGAAAGGACCTTTACACTGTAACTAAAACTTAATTTCAACATTGAAAACTATAAAAGATTTTGAGCACCAAATGTTGATGTTTAGAGATATTAAGTTGGTCTAAATTATAGTTTTGTACCCTCTGCTTA[T/A]GTCAGATGGGATGACAGACCAGGGCAACAGACTGTCCTATATTCTTATCAACCCTTCCCCTGACACACGCCTGGAGCTTCATGATGTCGTGTGAGTATACAAACATTACAAGCATTTAAGCTAAAATTATTATTATTGCTTCTAAGCTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATAAATATAATGCATATTGTTTGTTGTTATTAATATTACACACAACTGAAAATAATATGACTTATAAATAGTGGTGGTCCATTATCAGTGTTAACGTGTTGCGTTGATGCGAGTCTCTAATCGCGCAATAAAAAATATCATTGTTAATTTATTTTTTAAAGTTGGGTTGGGAGCTGGGTCTTTGTACACAAGCTATGATGACTTTCACCTTGATATTTTACCTCAGATGTATACCTGACCGGTGAGCAGC
Associated Phenotype:
Not determined