ZMP
LOC565691
Ensembl ID:
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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