ZMP
kctd13
Ensembl ID:
ZFIN ID:
Description:
BTB/POZ domain-containing protein KCTD13 [Source:RefSeq peptide;Acc:NP_001070619]
Human Orthologue:
KCTD13
Human Description:
potassium channel tetramerisation domain containing 13 [Source:HGNC Symbol;Acc:22234]
Mouse Orthologue:
Kctd13
Mouse Description:
potassium channel tetramerisation domain containing 13 Gene [Source:MGI Symbol;Acc:MGI:1923739]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16855 | Essential Splice Site | Available for shipment | Available now |
sa33115 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26011 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13226 | Nonsense | Available for shipment | Available now |
sa33114 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16855
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065807 | Essential Splice Site | None | 330 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 14832100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15077706 |
GRCz11 | 3 | 15227506 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGAGAACTTAATATTTGATGCACCTTATCGCGGTGGTGACCCAGCTCGG[T/G]AAGTGTTTTCCTCGTTGACAGCCAYTCTAATGACATCTCGAGCTAGCTGA
Long Flanking Sequence:
TTTTAGGATATTGAAAAATATTCTTAAATTTTATTAAAAATGTTTTTTCACAGAAGAAAATTCCAATCAAATATCTTATAAATGGTTTATATGTATATTTTTTTTATTTTATTTTTTTTATTTTATTTATTTATTTATTTATTTTCAGGATATAAGAAAATATTAAAAAATTTCGTAAAAATGTTACAGAAATGTGACCATTGTCCTGTTAAAAAACGCCCTTCACGATTGTCTGACTTTAGGTTGCAGGGGCGGGATTATATCGCTTGACAGACGTTGATGCGGGCCAATCAGTGACCGAGGGACACTCCTCGCGAGGTGGAGCAGCCATTGTCAACCCACAACAAGCAAGAAAGAGGAAGAAGACAGTTGAGCTGCGAGACAACAGAGGAAAATATGATTTGTAGAAAAATTATGACGAGTTTATTGTAAAAATACAACAGCCCGCTCGCGAGAACTTAATATTTGATGCACCTTATCGCGGTGGTGACCCAGCTCGG[T/G]AAGTGTTTTCCTCGTTGACAGCCATTCTAATGACATCTCGAGCTAGCTGAGAGGCTAATAATGAGCTTATCAATACACGACAGACCTCTTACGTGGTAAACAGATTCTCTACATGCATCTCTATATAACTGTCGAGTCGTTAAATAGCTGCATAATGGTGGGAAATCAATTTGGTGTGGTCTAGACGAGGATTAGCGAGATGTCTCAGCTGGAGTTAAGATCTTTGTGAATGTGTTGACCTAATTCTGTCCATTTCCCCTGGTATCAGGACAGAAACACATCTGTGTGGGGTGGACAGATATTCACAGACCCTCCAGAGTGTCACTAAACCAGTGTTATAACTCGCATGTTTGAGTTTTAAGGGATGAGATCACTAACGTTAGATGCTTTGTTATAGATGCTAAATACTTTGCTTTCTGATTGTTTTCTTTGTTGATGAGGTAAAGTTGGTTTTATATTCAGACATTTCGGATTTCTCCCTAATAAAATAACTTTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33115
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 |
---|---|---|---|---|---|
ENSDART00000065807 | Nonsense | 69 | 330 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 14828317)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15073923 |
GRCz11 | 3 | 15223723 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCACAGTCCAAACGCTCAGCAAAGAAGACAGCTTGCTCAGGAGTATTTG[T/A]GACGGGAGCACAGAGGTCAGCATCGACTCTGAAGGTAAGAAACAGCATGT
Long Flanking Sequence:
TTTTATCAAGAGTGATTATAAAAAATAAAATCTATACATTTTGACCATTAGAAGCTGCTTATATTCACAGACTTCTGCCACATAAATGTGTTTAAACCCTGTATAAAAGTGATTTTTGCATAATAGTTCTCCTTTGAAGTTGACCAAATTGCATGCCACTTGTTTTTAAATGTTTTGGGCCACCGCTCCATACCACTAATAATAACATCTCATAACCACCAAATTCTGTCTGCTTCGCATGTCTGTGTGTGTCTACAGGCAGCAGATAAGCAGTATTTGAGTTGTACTCCCCTGATGTCTGCCGAGGCATCTGGTTCGTCTGGTGGGCATGCGGTGACTGTGTCCGGGTCTTCCCCGTCATCCTCCAGCCATGTTGGGGAAGAAAAGCCTGGCAGGAGTCTGGTGAGCAGCAAGTACGTGAAGCTCAATGTTGGCGGAACTCTCCACTACACCACAGTCCAAACGCTCAGCAAAGAAGACAGCTTGCTCAGGAGTATTTG[T/A]GACGGGAGCACAGAGGTCAGCATCGACTCTGAAGGTAAGAAACAGCATGTGAATGTTTTGTTGTATGCTACTTTTTTAAAAGTTTGTAGTCAGTCGGTAGCTATGTTTCAATCCAAATATTTTTTTGCGCATTTTGGATGTGTGTATAAAAAAACGGTTCATGGAAACGCCAAGAAGCGCATCAATTTTGAAAATGAGCATAAAAAAGGATAAACTCTTTATTTAATAAGAAAAGATGCGCATAAACAGCAAAAAAAAAAACGCTTTTACCGAACAAATTCCAGTATGCACTTTAAAAAAGGTCATGTGATTTTGTTATAAGAGATCATGTGATGAAATAAACGTTTTTTAATAGACAAACCAACAGAATGACGCCTAAACAGTTTCAGTATTAGTGTAATTATATTATTATTACATCCAAAATTGTCAAGACTGTTTGTGCTCCGCATCTCACGCCTTCAAATATATATATATGTATATATATGTATATATATGTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26011
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 |
---|---|---|---|---|---|
ENSDART00000065807 | Nonsense | 85 | 330 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 14826402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15072008 |
GRCz11 | 3 | 15221808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATGCACATTTAAACATGTGTCCATTTGTATTGAAGGCTGGGTGGTGT[T/A]GGACCGATGCGGGAGACACTTTTCCCTGGTGTTGAACTTCCTGCGGGACG
Long Flanking Sequence:
TAGATTTTAAAATGTGATTTATTCCAGTGATCAGTTTCAGATTTCACTCTATTTACTCTCTCAATATGTTGATTTTCTGCTCAAGACGGATTAATACTTATAATTAATAGTATCAATGGAAATTTCTGGATTATTTTATGGCAAGAAATGTATTTACTTGAAGGAGAATGTTTTGTAACGGATGTCTTCACTTTCACTTTTCAATATAATATATTTTTCCTGAATAAAATTACTAATTTATTGTTTAAAATGCATTGTGACCTCTATAGGGTTTTAAAAATAAGTGGTACAGCTTCAAATCAAGTATAGCTCATTCTGTATGAATGCTTCCCCTGAATCAAAACAGACAAACACAAAAATTGAATGACAGAAATGTAAATCCACCAATCATGCTTCTTAATTTGATGTAGCGGTTAGCTAACTGAACTAACAGATGCAGAAACTAGCTCAGAGATGCACATTTAAACATGTGTCCATTTGTATTGAAGGCTGGGTGGTGT[T/A]GGACCGATGCGGGAGACACTTTTCCCTGGTGTTGAACTTCCTGCGGGACGGGACAGTTCCTTTGCCAGATAGCACGAGGGAGCTGGAGGAGGTGTTGAAGGAGGCGCAATACTACAGACTTCAGGGTCTTGTGCAGCACTGCCTCTCCACATTACAGGTCAGGCGTGTACCCTTAGACTTACTATGTTTATACTAGTGATTTCATTATCTTTTGTTGTTTGATTAATAATGGAAACACAGACAGCAAGAATAAGATGCTTTTACTGCATGCTTTTAAGATGCAGCACAGATGCAGAACAATGAGATAGTTACAGACAGCACAATTTCCTGAATGTTAACTTTTTTTTGAATGGTCGCCAAGTCATTTCGCTTCATAACTTTCATTCAGATTAGGCACTTCTCAGATCTGACATCAGCACATGCTCAAGGGACAAGCAAAGTCCACGCAAATAATACTTCAACAGGACAGTTCTATATAGTGTACCTTTTCCAGCTGCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13226
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 |
---|---|---|---|---|---|
ENSDART00000065807 | Nonsense | 146 | 330 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 14823002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15068608 |
GRCz11 | 3 | 15218408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTCCTGTKTAATGTTGATGCAGAAACGCAGAGATGTTTGCAGAGGTTG[T/A]CACATTCCTATGATAACTTCAGCCAAAGAGGAACAGAGGATGATAGCCAC
Long Flanking Sequence:
CGAGCTGACAGCCAATCTTTCCTAGGCTCAGCAAAACTTGCAAAAAATACCTCTGTATTCCTGCAACTGCAATATTTACTCAAATTTTTCTTATTCAAATCTTCAGCAACAATATTTAACTCGTGAATTTGTTTTACATTTATTTACACCTTGACCGATTTTTGTATGACATGGCCATTAAAAATACAATGTTCCTTAAGCAGATGGTTTTTAAAGTTACTTTTAAAGAGAATGTTACTTCAGTCATGTTGTTGTGATGTTTTGAAAAGACTAGTAACAATAATAATAAAAAAAAATCTAAATCGTAAATCGGTTAAACTTAATAAAAAAACCTAGATTTTGTTTTTTTTTGCCAAATCGCCCAGCCCTAGTCCAAAGCAGCTTGTGTCTACATAGAAGTGATATACTTCCTACTCAAAGTGTGTAGTGTTTGATTGATGTTGCTTATGAATGTCCTGTTTAATGTTGATGCAGAAACGCAGAGATGTTTGCAGAGGTTG[T/A]CACATTCCTATGATAACTTCAGCCAAAGAGGAACAGAGGATGATAGCCACCTGTAGAAAGGTAAGATATCAAAGGCTTATCATATTTACTTCCCTGCTGACTAAAACAACACATGAACACTGAGGTCTCCTCAGGCTTGAATACAAAACACAGTTTTTGCCTACAGCCCGACACTATCCAGTTACTGTCCAACTGTGTTCAGTATTTTATATTTGACATGACATTTGTCTACATTATAAGACTTTTAATTTAATAAAGAAATTGTATTTATTTTATTTTTTTGTTTGTTTTATCTTTTTTTATTTAATCAATTAATGTTAATTGAGGTATTTTATTAATTATATTTAATTTTTTAAAAATGTTATTATTATTTATTTTTGAATATTTAATTTATACATTTTATAACATTTATTCAAAATATTTTTATTTATTCAATATATGTTTTTTAATATATTAATTTAATTTATTCTTATTTTTTTGCTTAATTAGACTTTATTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33114
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065807 | Essential Splice Site | 184 | 330 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 14821809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 15067415 |
GRCz11 | 3 | 15217215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGAAACTGCAGAATAATAGAGGGAACAATAAATACTCCTATACCAGG[T/C]ACATTTGCCCTTTTTCTCACTCCTTCAGCCTTTTCAAAAATAACTTGTGT
Long Flanking Sequence:
ATTTCTTTTATAAATTTAATTTAATTTTATTAATTGTTCATTTTTTATTTTATTTATTTTATTTTATTTATTCTATTTAATTAATTAGTAATTTTTTATTTAATTAATTTATTTTATTAATAATTTCATTTATTTATTTTATTAATTAATTCGTTATTTATTTTGGCCATTTTATGTATTTGTTTATTTAATTATTAAAACAAAATTCTGTAAGCACTATCACTGTTGTCGTGTATAATTCCTGTTCAGATTTTAAGGCAAGACTGTACTGGCAAAACTATAGTTTATTATGCACATGTCAATTTTGCGTCTCCATAATAAAGTGTTATTTTAGAATAGTGAATCTAAATATATGTTTTGAAAAAAGAAAATGCCATATACTTTCTGTAAAATAACCTTTTTGTTGGTCTTTGTTTTTAATGAAAATCATCTTTTCTTCATAACAGCCAGTGGTGAAACTGCAGAATAATAGAGGGAACAATAAATACTCCTATACCAGG[T/C]ACATTTGCCCTTTTTCTCACTCCTTCAGCCTTTTCAAAAATAACTTGTGTCTGATTTTCTCTGATAATGTGAGCGTGAAATCTTATGAACCATATTGTGACACTGCAGTTTTAATGGGATTTGAACTCAGTGCAGTGTTAGTGTAAACAAAAGCTGTTTAAAGAAATCAAAAACAGGACATGAGACCACAAAACCAACAACTATAAAGCAAAGCATACATTTTTCTCATCATAGTCACAGTTCAAACGGTCATCAGAAACGTGACTTCTTGAAGCAGCTTTTAGTTTGTGTGTGACAGATTTAACAGAAGCTGAATGTATGATTCAAGAGGAAGAGAAAAATTGTTTAGTTTTTATACAAAATGTCCCTAAACACGTGCAGGTTTAATTTGATTTAACCTCTGGGTCTATTAGTGTAAACAAAAACTGTCTAAAGAAACCAATAACAGGATATGACATCACAAAATACAACTATAAAAGGACAGAGTGGCCAAGCGTGCA
Associated Phenotype:
Not determined