ZMP
LOC568267
Ensembl ID:
Human Orthologue:
KCTD17
Human Description:
potassium channel tetramerisation domain containing 17 [Source:HGNC Symbol;Acc:25705]
Mouse Orthologue:
Kctd17
Mouse Description:
potassium channel tetramerisation domain containing 17 Gene [Source:MGI Symbol;Acc:MGI:1920094]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42010 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42011 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42010
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078476 | Nonsense | 138 | 214 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 20152166)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18934010 |
GRCz11 | 12 | 19055884 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTGTGTTTCTCATACAGCAGGTACCGCCGAAGCATGTGTATCGGGTGT[T/A]GCAGTGTCAGGAAGAGGAACTGACCCAGATGGTGTCCACCATGTCGGACG
Long Flanking Sequence:
ATAATTCATTTCTTGCACTGTCTTCAGTTTGCAACATTATTTAGTTGCAAAAAAGGCATAGTAATAAAAATCTGTAATAAAATCGACATTTTGTTAAAAAGAGTGTGTCTGTGCCTTCAGGTGTGCTGGAGGAGGCAGAATTCTACAACATCACACCGCTGATTAAATTAATCAAAGAGAGGATTCTTGAACGCGACTCAAAGGCCACGCAGGTATGAGCAAACCTTTATCGAGCCTCCAATACAGTGCATTTGCTTCCTTCTATCTGTTATTTTTTTCCCAGTACTATATTTCAGTTGATCTCTTATTCTACTGTACATTTGTGACTATATTTGTGTGCTTATGCAACAGCCATCAGTCCTCCGCCCACTCTCGCTCTTTTATTTGATTTTTTCTCCATACTCTCCTATTGGCATCATCCCACTGCATTTCTTGCTCGCACTGTTTTCACCCTGTGTTTCTCATACAGCAGGTACCGCCGAAGCATGTGTATCGGGTGT[T/A]GCAGTGTCAGGAAGAGGAACTGACCCAGATGGTGTCCACCATGTCGGACGGCTGGAAGTTTGAGCAGGTCAGCGTGCGCGCCTGCCGAAAACCCCGCCCCGGACTGCTCTGGACTGTGGGTTGGACTGACACGGAGTTGATATCCCTTCCCCTGATCCTAATGCTCCCAGTGTCCAATTCTCCCCTCAGATTCAGAGTCCAGTAATGTAGCTAAAGTGTCAAAATAAACTTTTGGATTTTTTTATTTAAAGGGATTTTACAAGGTCAGTTGCACCAATTTTTCCTAATAATATTATGGTTTTTTAAATGGCAGACTATGGCTAGACTACTACTCAGTAGGTACTGCATTTAAATTTGAATTTACTGCTCGACCGTTAGAAAGTGCTTTCTATACAGTATGAATTTGAGCAGTATGAAACTCATACATACTACATCTACTATTTGATCATGATAGCATAACCTACACGCATTAGTTGTGTCGATTCACTCCCATTTATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42011
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078476 | Essential Splice Site | 160 | 214 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 20152234)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18934078 |
GRCz11 | 12 | 19055952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGACCCAGATGGTGTCCACCATGTCGGACGGCTGGAAGTTTGAGCAG[G/A]TCAGCGTGCGCGCCTGCCGAAAACCCCGCCCCGGACTGCTCTGGACTGTG
Long Flanking Sequence:
AATCTGTAATAAAATCGACATTTTGTTAAAAAGAGTGTGTCTGTGCCTTCAGGTGTGCTGGAGGAGGCAGAATTCTACAACATCACACCGCTGATTAAATTAATCAAAGAGAGGATTCTTGAACGCGACTCAAAGGCCACGCAGGTATGAGCAAACCTTTATCGAGCCTCCAATACAGTGCATTTGCTTCCTTCTATCTGTTATTTTTTTCCCAGTACTATATTTCAGTTGATCTCTTATTCTACTGTACATTTGTGACTATATTTGTGTGCTTATGCAACAGCCATCAGTCCTCCGCCCACTCTCGCTCTTTTATTTGATTTTTTCTCCATACTCTCCTATTGGCATCATCCCACTGCATTTCTTGCTCGCACTGTTTTCACCCTGTGTTTCTCATACAGCAGGTACCGCCGAAGCATGTGTATCGGGTGTTGCAGTGTCAGGAAGAGGAACTGACCCAGATGGTGTCCACCATGTCGGACGGCTGGAAGTTTGAGCAG[G/A]TCAGCGTGCGCGCCTGCCGAAAACCCCGCCCCGGACTGCTCTGGACTGTGGGTTGGACTGACACGGAGTTGATATCCCTTCCCCTGATCCTAATGCTCCCAGTGTCCAATTCTCCCCTCAGATTCAGAGTCCAGTAATGTAGCTAAAGTGTCAAAATAAACTTTTGGATTTTTTTATTTAAAGGGATTTTACAAGGTCAGTTGCACCAATTTTTCCTAATAATATTATGGTTTTTTAAATGGCAGACTATGGCTAGACTACTACTCAGTAGGTACTGCATTTAAATTTGAATTTACTGCTCGACCGTTAGAAAGTGCTTTCTATACAGTATGAATTTGAGCAGTATGAAACTCATACATACTACATCTACTATTTGATCATGATAGCATAACCTACACGCATTAGTTGTGTCGATTCACTCCCATTTATGAATTCTATCGTGGTGCATCATGGATACACGTAGCATGCATTGGATGCACAGTTTAGAATTTCGCCCGTAG
Associated Phenotype:
Not determined