ZMP
kctd16a
Ensembl ID:
ZFIN ID:
Description:
potassium channel tetramerisation domain containing 16a [Source:RefSeq peptide;Acc:NP_001032315]
Human Orthologue:
KCTD16
Human Description:
potassium channel tetramerisation domain containing 16 [Source:HGNC Symbol;Acc:29244]
Mouse Orthologue:
Kctd16
Mouse Description:
potassium channel tetramerisation domain containing 16 Gene [Source:MGI Symbol;Acc:MGI:1914659]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13200 | Nonsense | Available for shipment | Available now |
sa35689 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1375 | Nonsense | Available for shipment | Available now |
sa42391 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16517 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13200
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014411 | Nonsense | 143 | 285 | 1 | 1 |
ENSDART00000130103 | Nonsense | 143 | 412 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 24716493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 23515017 |
GRCz11 | 14 | 23812262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATAGTCACAGTGATTTTGACGAAGCATCCCAGGGAAGCGACCAGAGGT[T/A]ATATCCAGCCTCTTACCTGGAMGCGCGCGACCGACGCTACGGCTTCATCA
Long Flanking Sequence:
TTTACTTTCTGCACGCTGAAATCGAGTCGAAAACTTTTGCGTCTTCACGTTTTTTGAAGAGTAACACACCGAAATGGCCCTGACTGAAAATTGCAGGACTTATCAAACGCCCAAGGACAGTGGATGTGCTCAGAGTTGCTCTTCTGATGTGGTGGAGCTCAATGTAGGTGGACAGGTGTACTACACTCGCCATGTCACCCTCACCAGTGTGCCAAACTCACTGCTGGGTAAATTGTTCTCCTCTAAAAAAGACATTTCTAACGACCTCACGCAGGACATCAAGGGACGCTACTTCATCGACCGGGACGGATTTCTCTTTAGGTACGTGCTGGACTATCTCCGCGATAAGACTGTCGTCCTGCCGGATTATTTTCCGGAGAAGGGGAGGCTGAAACGCGAAGCTGAGTTTTTCCAGCTGCCCGAGCTCGTCAAAATCCTAACCCCAGATGATTATAGTCACAGTGATTTTGACGAAGCATCCCAGGGAAGCGACCAGAGGT[T/A]ATATCCAGCCTCTTACCTGGACGCGCGCGACCGACGCTACGGCTTCATCACGGTCGGGTACAAGAGCTCGTGCGCATTCGGGAGGGACACTGATCCCAAAGCCCGCGGAATACCCAAAATCTTCATTTGCGGAAGAGTCGGTCTGGCGAAAGAAGTTTTCGGCGACGCACTAAACGAGAGCCGGGATCCTGACAGACCGCCGGAGCGTTACACTTCTCAGTTTTACCTGAAGTTTCGCCACCTGGAGCGAGCGTTTGATATGCTCGCGGAGAGCGGGTTCCACATCGTCGCGTGCAATTCATCACTCACCACATCTCCCCACAACAGGCATGCTGATGATAGATACTGGTCCAACAACACAGAGTACGTCTTCTATCGTAAGTACAGCTTATTTACTCTTTACGTTGTATTACAAAAAGAAAGAAAATAAAGCCATTTGGCAATGCTGGGTAGTTACTGATCAGATGAGATGTAATCTGGATTACGTAATCAGATTACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35689
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014411 | Nonsense | 187 | 285 | 1 | 1 |
ENSDART00000130103 | Nonsense | 187 | 412 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 24716624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 23515148 |
GRCz11 | 14 | 23812393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGGACACTGATCCCAAAGCCCGCGGAATACCCAAAATCTTCATTTGC[G/T]GAAGAGTCGGTCTGGCGAAAGAAGTTTTCGGCGACGCACTAAACGAGAGC
Long Flanking Sequence:
AGAGTTGCTCTTCTGATGTGGTGGAGCTCAATGTAGGTGGACAGGTGTACTACACTCGCCATGTCACCCTCACCAGTGTGCCAAACTCACTGCTGGGTAAATTGTTCTCCTCTAAAAAAGACATTTCTAACGACCTCACGCAGGACATCAAGGGACGCTACTTCATCGACCGGGACGGATTTCTCTTTAGGTACGTGCTGGACTATCTCCGCGATAAGACTGTCGTCCTGCCGGATTATTTTCCGGAGAAGGGGAGGCTGAAACGCGAAGCTGAGTTTTTCCAGCTGCCCGAGCTCGTCAAAATCCTAACCCCAGATGATTATAGTCACAGTGATTTTGACGAAGCATCCCAGGGAAGCGACCAGAGGTTATATCCAGCCTCTTACCTGGACGCGCGCGACCGACGCTACGGCTTCATCACGGTCGGGTACAAGAGCTCGTGCGCATTCGGGAGGGACACTGATCCCAAAGCCCGCGGAATACCCAAAATCTTCATTTGC[G/T]GAAGAGTCGGTCTGGCGAAAGAAGTTTTCGGCGACGCACTAAACGAGAGCCGGGATCCTGACAGACCGCCGGAGCGTTACACTTCTCAGTTTTACCTGAAGTTTCGCCACCTGGAGCGAGCGTTTGATATGCTCGCGGAGAGCGGGTTCCACATCGTCGCGTGCAATTCATCACTCACCACATCTCCCCACAACAGGCATGCTGATGATAGATACTGGTCCAACAACACAGAGTACGTCTTCTATCGTAAGTACAGCTTATTTACTCTTTACGTTGTATTACAAAAAGAAAGAAAATAAAGCCATTTGGCAATGCTGGGTAGTTACTGATCAGATGAGATGTAATCTGGATTACGTAATCAGATTACAAAATGGAGTACTCGTAGTTAGATTATATTGCTTCTTAATATGAACATAATCAGATTACAGTTACTTTTTATGAATTACATGATTACATAGAGCATTAGTAACCCAACAGCATCCCACTTTTTTCTCTTATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1375
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014411 | Nonsense | 218 | 285 | 1 | 1 |
ENSDART00000130103 | Nonsense | 218 | 412 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 24716719)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 23515243 |
GRCz11 | 14 | 23812488 |
KASP Assay ID:
554-1287.1 (used for ordering genotyping assays)
KASP Sequence:
GAGAGCCGGGATCCTGACAGACYGCCGGAGCGTTACACTTCTCAGTTTTA[C/A]CTGAAGTTTCGCCACCTGGAGCGAGCGTTTGATATGCTCGCGGAGAGCGG
Long Flanking Sequence:
GGTAAATTGTTCTCCTCTAAAAAAGACATTTCTAACGACCTCACGCAGGACATCAAGGGACGCTACTTCATCGACCGGGACGGATTTCTCTTTAGGTACGTGCTGGACTATCTCCGCGATAAGACTGTCGTCCTGCCGGATTATTTTCCGGAGAAGGGGAGGCTGAAACGCGAAGCTGAGTTTTTCCAGCTGCCCGAGCTCGTCAAAATCCTAACCCCAGATGATTATAGTCACAGTGATTTTGACGAAGCATCCCAGGGAAGCGACCAGAGGTTATATCCAGCCTCTTACCTGGACGCGCGCGACCGACGCTACGGCTTCATCACGGTCGGGTACAAGAGCTCGTGCGCATTCGGGAGGGACACTGATCCCAAAGCCCGCGGAATACCCAAAATCTTCATTTGCGGAAGAGTCGGTCTGGCGAAAGAAGTTTTCGGCGACGCACTAAACGAGAGCCGGGATCCTGACAGACCGCCGGAGCGTTACACTTCTCAGTTTTA[C/A]CTGAAGTTTCGCCACCTGGAGCGAGCGTTTGATATGCTCGCGGAGAGCGGGTTCCACATCGTCGCGTGCAATTCATCACTCACCACATCTCCCCACAACAGGCATGCTGATGATAGATACTGGTCCAACAACACAGAGTACGTCTTCTATCGTAAGTACAGCTTATTTACTCTTTACGTTGTATTACAAAAAGAAAGAAAATAAAGCCATTTGGCAATGCTGGGTAGTTACTGATCAGATGAGATGTAATCTGGATTACGTAATCAGATTACAAAATGGAGTACTCGTAGTTAGATTATATTGCTTCTTAATATGAACATAATCAGATTACAGTTACTTTTTATGAATTACATGATTACATAGAGCATTAGTAACCCAACAGCATCCCACTTTTTTCTCTTATCATTTTTTCTTTCTAGTATGTCTTTCTAGTATGACTTTATTAGTATGTGTACAATTTGACCTAAAATGAGCCTATTTAGTTTACATTTCCCTGTTTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa42391
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014411 | Nonsense | 226 | 285 | 1 | 1 |
ENSDART00000130103 | Nonsense | 226 | 412 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 24716741)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 23515265 |
GRCz11 | 14 | 23812510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCGGAGCGTTACACTTCTCAGTTTTACCTGAAGTTTCGCCACCTGGAG[C/T]GAGCGTTTGATATGCTCGCGGAGAGCGGGTTCCACATCGTCGCGTGCAAT
Long Flanking Sequence:
AAGACATTTCTAACGACCTCACGCAGGACATCAAGGGACGCTACTTCATCGACCGGGACGGATTTCTCTTTAGGTACGTGCTGGACTATCTCCGCGATAAGACTGTCGTCCTGCCGGATTATTTTCCGGAGAAGGGGAGGCTGAAACGCGAAGCTGAGTTTTTCCAGCTGCCCGAGCTCGTCAAAATCCTAACCCCAGATGATTATAGTCACAGTGATTTTGACGAAGCATCCCAGGGAAGCGACCAGAGGTTATATCCAGCCTCTTACCTGGACGCGCGCGACCGACGCTACGGCTTCATCACGGTCGGGTACAAGAGCTCGTGCGCATTCGGGAGGGACACTGATCCCAAAGCCCGCGGAATACCCAAAATCTTCATTTGCGGAAGAGTCGGTCTGGCGAAAGAAGTTTTCGGCGACGCACTAAACGAGAGCCGGGATCCTGACAGACCGCCGGAGCGTTACACTTCTCAGTTTTACCTGAAGTTTCGCCACCTGGAG[C/T]GAGCGTTTGATATGCTCGCGGAGAGCGGGTTCCACATCGTCGCGTGCAATTCATCACTCACCACATCTCCCCACAACAGGCATGCTGATGATAGATACTGGTCCAACAACACAGAGTACGTCTTCTATCGTAAGTACAGCTTATTTACTCTTTACGTTGTATTACAAAAAGAAAGAAAATAAAGCCATTTGGCAATGCTGGGTAGTTACTGATCAGATGAGATGTAATCTGGATTACGTAATCAGATTACAAAATGGAGTACTCGTAGTTAGATTATATTGCTTCTTAATATGAACATAATCAGATTACAGTTACTTTTTATGAATTACATGATTACATAGAGCATTAGTAACCCAACAGCATCCCACTTTTTTCTCTTATCATTTTTTCTTTCTAGTATGTCTTTCTAGTATGACTTTATTAGTATGTGTACAATTTGACCTAAAATGAGCCTATTTAGTTTACATTTCCCTGTTTGAAAGTTAACATTCCAGCAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16517
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014411 | None | None | 285 | None | 1 |
ENSDART00000130103 | Nonsense | 410 | 412 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 14 (position 24753558)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 23552082 |
GRCz11 | 14 | 23849327 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CKTTTTCCGGAGAGGAAGTACATGTGGCAGTCGGAGCTCTTGAAAAAATA[T/A]CAGCTCTGAAATGATTTCCTGCAGGCTCGCTGGRCCTWTTAGAGCGACAC
Long Flanking Sequence:
ACTGTCAACAGCTGCACTGACTTCTGTTAAATCTTATTCGGCACTGACATTTGTGTTTTTTTGTGTGTGTTTTAAGGTGGTCCATCCGGATGGTCTTCTTCCCACTGCGACTGCTGCTGCAAGAGTCACAAAAGCGAGCGAGAAGGTGAGAGTGGCACTTCCCTTAATGAGCTCTCCACTTCCTGTTCTGAGACCCAATCAGAAGCCAGCTCTCCCCAGGAAACGGTCATCGTGCGTCCAGTCACCCGTCAAGGCAACATCCAGACTTTGGATCGACCGGTGAAAAAGGGTCCGACCCCAATCCCCAGGAGAACTGATCTGCTGCGCATTCGGACCACAGGCCCACGTGATGTCCTCGCCGGGAAGAGGAAACCAGCCAAGGAGAAGATGACCCCGGAGCAGGAGCTGGAGAAATGCATCCAGGACTTCCGACGGATTAAAATTCCAGTGCGTTTTCCGGAGAGGAAGTACATGTGGCAGTCGGAGCTCTTGAAAAAATA[T/A]CAGCTCTGAAATGATTTCCTGCAGGCTCGCTGGGCCTATTAGAGCGACACAACAAAGCTCTCAGCGCATAAGATGACATCATAACTCTTCTTTTGCTTGGGCTTAATTGGCTCGTCTGTGTAATCATGCAGCAAGATGCACAATTAACAATTCAGTGAACCTCAAGTGACTGCTAAAGGGACCAGTCCTGTTTTGATACCAAGCACAATGACATTAAGTCAGTTTCACAGCGTCTACACAGACTTCTAAAATGATAACGAATTGTATATAGACAGATTAATCACAAATATATATATTACCTGTTTAATTACTTGGTGCACGGACGGCACTTTTGTACAACATTCCCGCTGTAAATGCAGTGCACATAGGAGAACCATGGGGATTTGTTTACACCTGGTCTTAAATACGGTTTTCTCAGTCTCACTTCAAGTGGAAGATGCTAAATACAGATGCAAATGGGGTTGGAAAGGTTTTAAGCTTGTCCATTGTTGATTACGCGC
Associated Phenotype:
Not determined