ZMP
kctd16b
Ensembl ID:
ZFIN ID:
Description:
BTB/POZ domain-containing protein KCTD16 [Source:RefSeq peptide;Acc:NP_001122224]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1328 | Nonsense | Available for shipment | Available now |
sa3118 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa1328
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 |
---|---|---|---|---|---|
ENSDART00000022976 | Nonsense | 54 | 446 | 1 | 2 |
ENSDART00000126585 | Nonsense | 31 | 423 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 21 (position 39593182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 40921644 |
GRCz11 | 21 | 40944691 |
KASP Assay ID:
554-1242.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGATGTTATTGAATTAAACGTGGGGGGACAAGTCTATTATACACGTTA[T/A]ACTACGTTAATCAATACCCCTGGCTCTCTTTTGGGAAAAATATTCTCTCC
Long Flanking Sequence:
TTGGATTCAGATCGTTGCTTAATTTGGAATAAACTTTGTTTCTCCTTGAAAGATTAAATGGTTTTATTATATGATGTTTTTAAATGCTTATGCAAATGCACTAGTTTTTTTTTTTCAGGCAAGGAAGCACACCCCAGTGTTTCGCTGTGTGCCCTGCTGAGCTACCAATTCTTCGACTCTAGGATGTAGGTGTGCAGTTCCTCGGATATTTTGCTCTTTCTCTTTTTTTGAGCCCTGTGGAGAATATGTGCATTTAAAAATATGTGCAATTATCGGTTCAGATTTGAAATGTGATTTCTTTTGCAATTTAATGTGCATAAAAATCGACGTTTCCTAAAACACTCCCGAATCTGTGGATCATTGGAAAAGAGCAGAACTTTGTTGTTATTTGCACCCATCACTGAAACGATGGCGTTGAGTGGAAATTCTAAACCTAAAGACAGCTCTTTTCCAGATGTTATTGAATTAAACGTGGGGGGACAAGTCTATTATACACGTTA[T/A]ACTACGTTAATCAATACCCCTGGCTCTCTTTTGGGAAAAATATTCTCTCCCAAAAATAATGCATCGAATGATCTTGCCAGGGACCCTAAAGGTCGTTATTTCATCGACCGGGATGGTTTTTTGTTCAGATACGTGTTAGACTACCTCAGGGATAAACAGGTTGTTCTTCCTGACCACTTTCCAGAGAAAGGAAGGCTGAGGAAAGAAGCGGAATACTTTCAATTGCCTGACTTGGTTAAACTCTTAACCCCTGACGACCTAAAACCTAGTTCCGATGAATATATCCACAGTGATTACGAGGACGGGTCTCAAGGAAGCGATCAGCGAATGTGTCCTCCGCCGTCACTCATTCTCGCCGACAGAAAAAGCGGATTCTTAACCGTCGGATATCGCGGGTCTTGTACAATGGGTAGGGAAAATCGAACCGATGCCAAATTCCGGAGGGTGCCTCGGATTATGATATGCGGCAGGATTGCCCTGGCCAAAGAAGTTTTTGGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3118
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000022976 | Nonsense | 407 | 446 | 2 | 2 |
ENSDART00000126585 | Nonsense | 384 | 423 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 21 (position 39608067)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 40936529 |
GRCz11 | 21 | 40959576 |
KASP Assay ID:
554-2796.1 (used for ordering genotyping assays)
KASP Sequence:
AAGTTCCCGAGACACTAGCACCTGCAAGAAACGGCCAGCAAAAGAAAAGT[T/A]GTCTGTGGAAGAGGAGCTGGAGAAGTGCATCCAGGACTTTCGCAAGATCA
Long Flanking Sequence:
TGATTGTTGATGAAACAGAGCTCGGGGCTCTCTCCCAGGACAGCATGCCAAACAAGCTTTATAATCAATCATCTACTAAGTGTGAACTCTTGAATGTTATTGTGCTCACATCCATGTGTTTAAACTGTTTTTAAAAAAAATTTCTCTACCTCCAGGTGGTCCATCTCGCTGGTCATCTCCGCCTTGCGAGTGTTGCTGCAAGGGACACAAAGGTGAAGCTGAGGGTGAAGGTGAGAGTGGAACCTCTTTCAACGAGCTCTCCACTTCAAGCTCAGAGAGTCATTCTGAGGCCAGCTCTCCACAAGGTACCGTCATCTGTGGCCCGGTGAGCCGGCAAACACATGTGCAAACATTAGATAGGCCTCCCAAGAAAGGTCCTGTTCAACATCTCCTGCAGCAGCAACAGTCCGAGCATCGCCGTAAGAGCGACCTTCTCCGGACCCTCACTGCAAGTTCCCGAGACACTAGCACCTGCAAGAAACGGCCAGCAAAAGAAAAGT[T/A]GTCTGTGGAAGAGGAGCTGGAGAAGTGCATCCAGGACTTTCGCAAGATCAAGATTCCTGAGCACTTCCCAGAGCGCAAGTACATGTGGCAGGCTGACCTTCTACGCAAATACCGTCTCTGAGGGATAGCAGCTTTCGACTGTAAAGTGCAAGTTACAATAATTCATGTTCACTACCACTACTATTGCTAGTCTACTCACACTACTACTGCCTTTTGTCAGTGTTGGCTGATATACCAAGTGACCCCTTCGTCTTCTAGAAAACCAATTGTTTACTTGCGTTGTTGGTTTTGCTCCCTTGCTGAGCTACACATATTTACGTTTAAGTGTGTGTTTGTTACAACTGAATTCTTGACCTCAGTATGTTAGGGCCTACTCACACTATGCCATCCGTACCGTGCCCAGGCCCGTTTCCCGGATCATTTGAGAAGTGTGAGTGCGCTGAATCGGGCTTAAGCACGGTTCACTTGGCCGGCCCTGGCCCAGTTGGAAGAGGTGTGCC
Associated Phenotype:
Not determined