ZMP
kcnh8
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate potassium voltage-gated channel, subfamily H (Eag-related), memb
Human Orthologue:
KCNH8
Human Description:
potassium voltage-gated channel, subfamily H (eag-related), member 8 [Source:HGNC Symbol;Acc:18864]
Mouse Orthologue:
Kcnh8
Mouse Description:
potassium voltage-gated channel, subfamily H (eag-related), member 8 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23505 | Nonsense | Available for shipment | Available now |
| sa31032 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32242 | Nonsense | Available for shipment | Available now |
| sa39241 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23505
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 |
|---|---|---|---|---|---|
| ENSDART00000090810 | Nonsense | 245 | 996 | 5 | 16 |
| ENSDART00000132914 | Nonsense | 245 | 694 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 19 (position 21052215)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 20985595 |
| GRCz11 | 19 | 20569918 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTTCTGGCTACCTTTTATGTGGCTGTTACGGTGCCGTACAATGTTTG[T/A]TTTATAGGTGATCAAGATTTGACACGCAGCACCACCGTCACTGACATTGC
Long Flanking Sequence:
TTAGTACATTATACTTTTAAAAGTATTTTGAATGTATACTTAAAATAAAAAAGTATACATTCATACTTTCTATACTTAAAAGTAAAAAAGTATATTTTAAAAGTATATTTTTAGTGTGTACAGAATGTTAAATGCACAAGCTTATTTTCCAAAACAAAAGTTCAAAACTCAAACACAGATTCACTTTACTAGAAAAAAGCCGAAAGTGGATTAAAGAGACACATGTAAACATCAGGTGTGAACAACAAGGTGTCTTTCTTGTCAAATCAACCAGATTGCATCCTAATTCCAGGGCCAAAAAACATGTTAACTTACACAAATTGTTCTCTCTTTTTCTAGAATGTGTTTGGGGATCCACCCGCTCTGCCTGAATATAAAGTCGCTGATGCCAAGAAATCCAAGTTCATTCTTCTCCACTTCAGCACCTTTAAAGCAGGCTGGGATTGGCTGATCCTTCTGGCTACCTTTTATGTGGCTGTTACGGTGCCGTACAATGTTTG[T/A]TTTATAGGTGATCAAGATTTGACACGCAGCACCACCGTCACTGACATTGCTGTTGAGATACTCTTTATCATTGGTAAGACATTATTTTTAGTTGGTCCATTACATAGTACATTTTTCATTGTGAGCATGATTATGATTTATGTGATTATATTACATCTGTATCTTTATATATGATTAGAATCAGGTCTTTAAATCAGTTTCATGGTCTTTGACTTCCTCCATTAACTCAGTCTTATACCACAGGGAAACACACTGCATCATTCTCCTTTAGTTGTGGTGCATTGGAGAAAAAAATATACTGTGTTATTGGAATTAAAAAGGGTAACTTGTACAAAAATAAATAATTATTATTTTTTTTTAAACAGAAGTTGTTTAACCTTCTTTTGCTGTACATAAGAGCATATTTTTATATACTCTTAACCACCAGCAGTGTCACAATGGCATAAAGTAATGGAAGATCACCATAAACCCTGGTTATTTATTTATTAATGATTATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31032
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 |
|---|---|---|---|---|---|
| ENSDART00000090810 | Nonsense | 707 | 996 | 13 | 16 |
| ENSDART00000132914 | None | None | 694 | None | 12 |
Genomic Location (Zv9):
Chromosome 19 (position 21108097)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 21041477 |
| GRCz11 | 19 | 20625800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCAATCACAGATGGAGGGGAGGGGAAACGGAGATGCGATCCAGTGCTA[T/A]CCACCAATAGCTGAGCATCACAATGAAGAAGATGACGATGACGACGACGA
Long Flanking Sequence:
AAATGACTTAAATCCAAAAAAAAAAAACCCCTTGGAACACAAGTGCAGTACAGTTCATACCATTAGCATATTAGACTACAGCAGCACAAGTGCAGTAAAGACTTGTTTTTACTCCGGTTTACAGACTGCTGTTGAACGTTTAATGTACTGTATTTGAAATGTATTTATACTTCATTGTATTGAAATTTTGCAATTGTACTTACTTTTACTGCAGTTATAGGTCTTTATACTGCTGTTGTACTTTAGTTGTACTGCAGTTTTACTTCAGTTCTTTTTTGTAAGGGGTGTAAGGGACTGCTTAAGAACAAACTCACTGCTGCATTAACAAAATGTTCGTACATCTCCTTGTTTAATCGTAATAACAAAAGCCGTTCTTTTCATGTTGAGTCATTCAAGGTTATTTATCCAACATTTATCTGACCTCACATGAACCTCAGAGAAATCTCCTCTGTCCAATCACAGATGGAGGGGAGGGGAAACGGAGATGCGATCCAGTGCTA[T/A]CCACCAATAGCTGAGCATCACAATGAAGAAGATGACGATGACGACGACGATGAAGATGATCAGATACAGTACCTCAGCGGTGGAGGCAAACAGAAAACACACATGCAGAAAAATGATCACCAAACCAACAAAAAGCTCCACATTCAGCACACCACTGTCACGAAACCTGACCTCGGAAATCTCAGCCCAAGGTGTGCGCTTGACCACACATGCATGCATTTCAAAAAAACATTTAAAGGAGATTCTGGATTTTAATAGTCATTTGCTCACTGGTGCTTGAAGGTCTTTGGAGAAATGGTTAAGTGGATTTCTGTTTGTGTGTGTTCAGGGTCGTGGACGGCACGGAGGACAGTGATGGCACAGAAAACTCCCACACGTTCATATTTTCCTCTGCTCATCAGCACAGCGTCAGTGGTGCGACCAACACCACTGCCACCACAGCAGGTGTGTGAGCGAGTGTGTGTATGTGGCGGAGTGTGAGTTGTTAAGGTGCCTTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32242
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090810 | Nonsense | 752 | 996 | 13 | 16 |
| ENSDART00000132914 | None | None | 694 | None | 12 |
Genomic Location (Zv9):
Chromosome 19 (position 21108230)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 21041610 |
| GRCz11 | 19 | 20625933 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCAAACAGAAAACACACATGCAGAAAAATGATCACCAAACCAACAAA[A/T]AGCTCCACATTCAGCACACCACTGTCACGAAACCTGACCTCGGAAATCTC
Long Flanking Sequence:
GAACGTTTAATGTACTGTATTTGAAATGTATTTATACTTCATTGTATTGAAATTTTGCAATTGTACTTACTTTTACTGCAGTTATAGGTCTTTATACTGCTGTTGTACTTTAGTTGTACTGCAGTTTTACTTCAGTTCTTTTTTGTAAGGGGTGTAAGGGACTGCTTAAGAACAAACTCACTGCTGCATTAACAAAATGTTCGTACATCTCCTTGTTTAATCGTAATAACAAAAGCCGTTCTTTTCATGTTGAGTCATTCAAGGTTATTTATCCAACATTTATCTGACCTCACATGAACCTCAGAGAAATCTCCTCTGTCCAATCACAGATGGAGGGGAGGGGAAACGGAGATGCGATCCAGTGCTATCCACCAATAGCTGAGCATCACAATGAAGAAGATGACGATGACGACGACGATGAAGATGATCAGATACAGTACCTCAGCGGTGGAGGCAAACAGAAAACACACATGCAGAAAAATGATCACCAAACCAACAAA[A/T]AGCTCCACATTCAGCACACCACTGTCACGAAACCTGACCTCGGAAATCTCAGCCCAAGGTGTGCGCTTGACCACACATGCATGCATTTCAAAAAAACATTTAAAGGAGATTCTGGATTTTAATAGTCATTTGCTCACTGGTGCTTGAAGGTCTTTGGAGAAATGGTTAAGTGGATTTCTGTTTGTGTGTGTTCAGGGTCGTGGACGGCACGGAGGACAGTGATGGCACAGAAAACTCCCACACGTTCATATTTTCCTCTGCTCATCAGCACAGCGTCAGTGGTGCGACCAACACCACTGCCACCACAGCAGGTGTGTGAGCGAGTGTGTGTATGTGGCGGAGTGTGAGTTGTTAAGGTGCCTTTAGTTTGTGGCCAAAATTTTAAGGCTGACACACAATAAAATTTTCAGTATTTATTATTAGAAGTGTAATGGTACACAAAATCTATAACGCATCTTGTATTTTAAGTCACAGTTCAGTTTCATTACACTGTCTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39241
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090810 | Nonsense | 821 | 996 | 15 | 16 |
| ENSDART00000132914 | None | None | 694 | None | 12 |
Genomic Location (Zv9):
Chromosome 19 (position 21112386)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 21045766 |
| GRCz11 | 19 | 20630089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTTCTCTGTGCAGAATTAGCTGCTAAATCGGAGGACACCCGAGGA[C/T]AGCTACGCCATCTTAACCAAGAGGTAAATTATTTTCTGCTCATTCTCTGC
Long Flanking Sequence:
TAAAATTAATTAATTACAATCAAAGACAAGAGACAGAAGGTGATCTTTTAGATGAGACTTAAAAGCACCAAGTGAAGAACAAGACCTGATATATAAAGGCAGACCATTCCACAGTCGGAGGGCTGCAGCAGAAAAAGCCCTGTTTTCTCTTGATTTCAACCGTGTTTTTGTGCATCTCACACATTCTCATCTGTTTGAGTTACAGGATTATTGTTAAATCCTTTTTGGACTTTGCCATATTGAATGACGGCCTGTTTTAATAAGAAGATTGCAGCTTAGACATTCTGCAAAATCATTACATTTCTGTTTCTTAGAAGAAAGAAAATCACACCAGTTTTTGATAGACATGAATGATGAGTTTTCATTTTTGTGGTGAACTCTTCCCTGAAGTCTTTGTAATGGGTTTTCCCTGGATGTTCTATCAGTGTGAGGCAGTTGGACATAATTGTTTTTTTTTTCTCTGTGCAGAATTAGCTGCTAAATCGGAGGACACCCGAGGA[C/T]AGCTACGCCATCTTAACCAAGAGGTAAATTATTTTCTGCTCATTCTCTGCCAGTCATGTTATTTTGTTGTTTTTGCTGTGTAATTAAATGGTAGATCTTCACTTACAGTACAGTTTGTATGGGATATCTTTCCATGGACTGTGGATTGTATAGGGGATAACTCTGAGCTTAATACGAGTACCGACAGATCAATACCAGTGCAGCTCAGGTGAACTCATGGTGCCAGGTATGCACTAGCCATATGGCAGGCTTCTGGGAGAGAGGAAAAGGGGGATGTTATTCAAAGACTAGAGGACATAAAACTCATTAGAAGAGGAAAGTGGGGCTGGCCCCATGATGATGGAAGAGGACTTTCCAACATCCCAGATTTCCACAGTGCCCTTGAACCCTCACCACATGTAGTTTCCCAGGCATTGCACACATGCATGTTTCAACATAATTCATTAGCTCGTTGTAAATTATACTAATTGGCGCAAGAGACATTGCTTGAATTGGAAGGC
Associated Phenotype:
Not determined