ZMP
si:ch211-11o22.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate potassium voltage-gated channel, subfamily H (Eag-related) famil
Human Orthologue:
KCNH3
Human Description:
potassium voltage-gated channel, subfamily H (eag-related), member 3 [Source:HGNC Symbol;Acc:6252]
Mouse Orthologue:
Kcnh3
Mouse Description:
potassium voltage-gated channel, subfamily H (eag-related), member 3 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41434 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21499 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41434
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 |
|---|---|---|---|---|---|
| ENSDART00000090625 | Nonsense | 521 | 874 | 12 | 18 |
| ENSDART00000146284 | Nonsense | 577 | 914 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 28976514)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 28132210 |
| GRCz11 | 9 | 27942956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTTCATCCGTGTGCATCGACTGCCCAAAGCCCTTGCGCAGCGCATGT[T/A]GGAGTGCTTTCAGACCACATGGTCCGTCAACAATGGCATTGATGTCAGCG
Long Flanking Sequence:
TTGCCTTATTGGTTTTTACAGTACTCGGTTGATTTGAGTTCTCTTCGTTTATTGGGTTTTACTGTGCTCAAATAGCTTCTTTGCTCAAATGAAGTTCACAGTACTCATTAGGATTATTGTTTTAACTCAAATGGTTTGTTGCAATCGATTTTCCTCAAATGGTTTGAGTGACAATGTTTTTTTTTAGTTAAAAACATATAAAAAAAATTAATTATCAGCATTTTTATTTAATTTCTGGAATTTTAATTCATGATCCAGATACCTTGAACAATCTACTGTAAGGCACATAGATGTAAAGTTTTTAAAAGAAGTTATAAATTGACCTGAAATGTTTGTTGTGTGTCTCTCCTCAGCACTCATGCACGCTGCAGTCTTCGGTAACGTGACGGCCATTATCCAGCGGATGTACTCGCGCCGCTCACTCTATCACACTCGAACCAAAGACCTCAAAGACTTCATCCGTGTGCATCGACTGCCCAAAGCCCTTGCGCAGCGCATGT[T/A]GGAGTGCTTTCAGACCACATGGTCCGTCAACAATGGCATTGATGTCAGCGAGGTATGACCTTAATGTTAATACTTAATAATGTTTTTCATAATTGGTGTGCAGGAAAGACTCAGTTGGATAATATGTTAGCAGTATGAGAGCTGCTCTTCTTAACTAATCTTTGAACTTGAGCAGATTCTTGACATGATTTATGAAAATGTTCACAATATGTTTTTTGTGTTTTCTTATTTAATTAATGGTCAGTGAAAAAGGTCAGACTGTTTACAAGTTGTTAAATTTTAAATTATTTAGCATTATTTTTGTTTTTTGAAGTTGTACATTTATATATATAAGTAAACATTAAATCAGGGGTGCCAACACTTTTTCGTATGAAGAGCCAAAAACCAAATATCATTGAGAGCCATGGGCCAAAGATAAACATACCAAACTATTTGACATTGAAGTTGCCATGGATCATTTCTTAATGTATTTAATAATATTTTAAAACAAATAGAAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21499
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090625 | Essential Splice Site | 621 | 874 | 13 | 18 |
| ENSDART00000146284 | Essential Splice Site | 677 | 914 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 9 (position 28974093)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 28129789 |
| GRCz11 | 9 | 27940535 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGGGCTCCATGGAAGTGCTCAAGGACAACACTGTGCTGGCTATACTGG[G/A]TAAGATCATACTCACCATGCCTAATATCCGATAGCCAGAAAGTGATTCAT
Long Flanking Sequence:
CTTACACTCACAATGTATTTAATGAGCTCAATTCAAAACACTCGTTGCGTAACTCGTAGCTCATAACTTACTCTCTCCTTCTGATTTGATATCCAATATCATCTCCAATTAAAGTTCAAGTAGAAGACTGATCTGCGGTTTCGTTGCCGCAGTCTCCTTGACGATCAGCCGTGAATCAAAAGTTTGTGATTCTTTTCAAGGTTGAGAAGTACGAGTACTTGAAATAAAATGCCTCTTTGTCCTTTTGCAGCTTCTGAAGGACTTTCCAGATGAACTGCGGGCCGACATCGCCATGCACCTGAATAAAGAGCTGCTGCAGCTGCCTCTGTTTGAATCGGCCAGTCGAGGGTGCCTGCGATCGCTCTCTCTCATTATCAAAACCTCTTTCTGCGCTCCAGGAGAGTTCCTCATCCGCCAGGGTGACGCTCTGCAGGCCATATACTTTGTCTGCTCGGGCTCCATGGAAGTGCTCAAGGACAACACTGTGCTGGCTATACTGG[G/A]TAAGATCATACTCACCATGCCTAATATCCGATAGCCAGAAAGTGATTCATTTTTTTATAAATTGTTAAAATTTTGGTATTTGTGATGCAGCAAGCCCAGAGATTGTTGATTGAATTGTAGATGAATTAAAAGTGATCATAAAAAAATAATTTATCAACTGAGTGGCGGCTTGGACCCGGAAACAAGTCATCACTTACAAGGCGGATTAATACGATAATACTATATTTTTTGAGCACTGCTGGGTAGTGTTTGTCATTAGAAAATATACATTTTAAAAGGGTCAACATCATCATCATCTTACACTTTTTTATTATTTATTATGTCTGGCACAGTGGCAGTAAGTTATTTATTATTTATGGATTCTATCTATCTCCATTTTTGGCAACACTTTAGAATAGGAGTTCATTAGTTTATGCATTCACTAATGAATAATCTTGTATAGTATTTATTAATTGTAGTTCAACATTTACTAATGCGTTATTAAAATCCGGAGTTGTGTT
Associated Phenotype:
Not determined