ZMP
kctd1
Ensembl ID:
ZFIN ID:
Description:
Novel potassium channel tetramerisation domain protein [Source:UniProtKB/TrEMBL;Acc:Q5SNS9]
Human Orthologue:
KCTD1
Human Description:
potassium channel tetramerisation domain containing 1 [Source:HGNC Symbol;Acc:18249]
Mouse Orthologue:
Kctd1
Mouse Description:
potassium channel tetramerisation domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1918269]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa7468 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7468
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 > C
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111063 | Missense | 60 | 271 | 2 | 5 |
| ENSDART00000144172 | Missense | 109 | 285 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 18279161)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 18333661 |
| GRCz11 | 20 | 18233244 |
KASP Assay ID:
554-4137.1 (used for ordering genotyping assays)
KASP Sequence:
CGTGCACATTGATGTCGGAGGTCACATGTACACCAGCAGCCTGGCCACAT[T/C]AACCAAAYACCCCGAGTCCAGGTAAATGACTGTACACACACAGAGATAAA
Long Flanking Sequence:
AGAAATGGACAGATAGACCCACTGTGTCTGTCATGAGATGTCTGATGCGGCTTTACCGAGCTCAACATTTTTGGCTGAGCTGAGAAATATAAACGAAAATGGTGTTGGCTTTTTTAGAGAAGGTGGAGGAACTGCTCCATATGTCCAATCCTATTTCAGTGAAAATTAAACCAACATGTTGAATAACGCTGCCTGTTTCAGGGCACCATTAATGTCCATTTTTCACATTCCAGTCAATTCCTGATGTTTCATCTCAATTATTTGACCTCCTTTTCTGCTTTGCCTATACATTATTTAATTGAACTGATCTTAAACACATTTTCTCTTTTAGGAAAATCGCAGCAACAGTGTGGGCATGTCGACTCGGCCTATCTTGGCACATTCGCCGGTCTCGCCGCTGGGCACAGCTGGCATCCCCACACCTGCACAGCTCACGAAGGCCAACGCTCCCGTGCACATTGATGTCGGAGGTCACATGTACACCAGCAGCCTGGCCACAT[T/C]AACCAAATACCCCGAGTCCAGGTAAATGACTGTACACACACAGAGATAAACACAAAAACAAGTGGACCCTTTTCCATTTCTTGTAGTTTTTAGAAGTGGAATTCATCGTAGTTATTTTATTCATATCCTGTGCTCCTGTAGAAAAACACATATTTCATGATAGCTATTACAGGACTTTACAAATGTAACTTTTTTTGGTGAGATCAACTATCAGTTGTGTTCAGAAATACCCCAAAAACATTGTTCAGCATGTTATAGATCACTATTTTCCAGTAATAAAATGAATACATAAAGCTAAACATAGGTATGGGGCAGCCCGGTGGCGCAGTGGGTAGCAATCTTGCCTCACAGCAAGAAGGTCGCTGGTTCAAGCCTCGGCTGGGTCAGTTGGCATTTCTGTTTGGAGTTTGCATGTTCTCTCCATGTTGGCGTGGGTTTCCTCTAGGTGCTCCGGTTTCCCCCACAAGTCCAAAGACGTGCGCTATAGGTGAATTTGGGTA
Associated Phenotype:
Not determined