ZMP
kcnd1
Ensembl ID:
ZFIN ID:
Description:
potassium voltage-gated channel subfamily D member 1 [Source:RefSeq peptide;Acc:NP_001119942]
Human Orthologue:
KCND1
Human Description:
potassium voltage-gated channel, Shal-related subfamily, member 1 [Source:HGNC Symbol;Acc:6237]
Mouse Orthologue:
Kcnd1
Mouse Description:
potassium voltage-gated channel, Shal-related family, member 1 Gene [Source:MGI Symbol;Acc:MGI:96671
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41128 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41129 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41128
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114765 | Nonsense | 75 | 632 | 1 | 6 |
| ENSDART00000133985 | Nonsense | 75 | 632 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 10412921)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9829503 |
| GRCz11 | 8 | 9868088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCGATATCCCGACACTCTGCTGGGCAGCTCGGAAAAGGAGTTTTTCTA[C/A]AACGAGGACACTCAGGAGTATTTCTTCGACCGGGATCCAGAGATGTTTCG
Long Flanking Sequence:
GTTGACTCTTTAGGCAGCCACAATCTCCAAACAAAACAGGGTAATTTTGGAATGTTTTTTGATATATGGAGATCCTAAGATGGAAATTTGACGGCCTTCAATTTTGGTAGCAGATAATAAAAACCTACACTTTCTAGTGTATCGCAAGCCGAAGTATACATAACTAACAAATCTGAGATGCTCAGCTCGGATGATTAGCTCGAAAAGACTCCGAAAATCTTCTCAGGTCTGACTGGCGTTTTCCTGCTTTAATTCGTTGACAACGTTTCGTTAAAGATGGCTGCCGGAGTGGCAACATGGCTACCGTTTGCCAGGGCAGCAGCCGTTGGCTGGCTTCCCCTGGCCAAGAAAACCATGCCCAAACCACCAATAGACAAAAAAAATCGCAACGATGAGATCCTGTTTGTAAATGTGAGCGGACTCCGCTTCCAGACATGGAAAAACACGCTAGACCGATATCCCGACACTCTGCTGGGCAGCTCGGAAAAGGAGTTTTTCTA[C/A]AACGAGGACACTCAGGAGTATTTCTTCGACCGGGATCCAGAGATGTTTCGCCACATTTTGAACTTCTACCGAACAGGCCGGCTTCACTACCCCCGGCAGGAGTGCATTCAGGCCTTCGACGAGGAGTTGGCGTTCTACGGCATCGTGCCGGATATTATCGGAGACTGCTGCATGGAAGAGTACAGGGACCGCAAGAAAGAAAACCAGGAGCGTTTGGCAGTAGACACGGAGGCGGAGATGGCGACAGACACCCCTCTGCCGCCACACAGCACGCATCGGGAACGCTTGTGGCGTGCGTTCGAGAATCCCCACACTAGCACCATGGCACTGGTTTTCTACTACGTCACCGGTTTCTTCATCGCCGTCTCAGTCATAGCAAACGTAGTAGAGACCGTCCCATGCCGACCGCTCAAAGGCAGCAAGAAAGACTTGCCATGCGGAGAGAAGTACTCGCTGGCGTTTTTCTGCATGGACACGGCCTGTGTGCTCATCTTCACCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41129
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 |
|---|---|---|---|---|---|
| ENSDART00000114765 | Nonsense | 109 | 632 | 1 | 6 |
| ENSDART00000133985 | Nonsense | 109 | 632 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 10413021)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9829603 |
| GRCz11 | 8 | 9868188 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCACATTTTGAACTTCTACCGAACAGGCCGGCTTCACTACCCCCGGCAG[G/T]AGTGCATTCAGGCCTTCGACGAGGAGTTGGCGTTCTACGGCATCGTGCCG
Long Flanking Sequence:
ATTTTGGTAGCAGATAATAAAAACCTACACTTTCTAGTGTATCGCAAGCCGAAGTATACATAACTAACAAATCTGAGATGCTCAGCTCGGATGATTAGCTCGAAAAGACTCCGAAAATCTTCTCAGGTCTGACTGGCGTTTTCCTGCTTTAATTCGTTGACAACGTTTCGTTAAAGATGGCTGCCGGAGTGGCAACATGGCTACCGTTTGCCAGGGCAGCAGCCGTTGGCTGGCTTCCCCTGGCCAAGAAAACCATGCCCAAACCACCAATAGACAAAAAAAATCGCAACGATGAGATCCTGTTTGTAAATGTGAGCGGACTCCGCTTCCAGACATGGAAAAACACGCTAGACCGATATCCCGACACTCTGCTGGGCAGCTCGGAAAAGGAGTTTTTCTACAACGAGGACACTCAGGAGTATTTCTTCGACCGGGATCCAGAGATGTTTCGCCACATTTTGAACTTCTACCGAACAGGCCGGCTTCACTACCCCCGGCAG[G/T]AGTGCATTCAGGCCTTCGACGAGGAGTTGGCGTTCTACGGCATCGTGCCGGATATTATCGGAGACTGCTGCATGGAAGAGTACAGGGACCGCAAGAAAGAAAACCAGGAGCGTTTGGCAGTAGACACGGAGGCGGAGATGGCGACAGACACCCCTCTGCCGCCACACAGCACGCATCGGGAACGCTTGTGGCGTGCGTTCGAGAATCCCCACACTAGCACCATGGCACTGGTTTTCTACTACGTCACCGGTTTCTTCATCGCCGTCTCAGTCATAGCAAACGTAGTAGAGACCGTCCCATGCCGACCGCTCAAAGGCAGCAAGAAAGACTTGCCATGCGGAGAGAAGTACTCGCTGGCGTTTTTCTGCATGGACACGGCCTGTGTGCTCATCTTCACCTTCGAGTACCTCATGAGGCTTTTCGCCGCCCCTAGCCGCTGCAAGTTCATGCGTTCAGTCATGAGCGTGATTGATGTGGTCGCCATCATGCCCTACTACATC
Associated Phenotype:
Not determined