ZMP
kcnh1
Ensembl ID:
ZFIN ID:
Description:
potassium voltage-gated channel subfamily H member 1 [Source:RefSeq peptide;Acc:NP_001038396]
Human Orthologue:
KCNH1
Human Description:
potassium voltage-gated channel, subfamily H (eag-related), member 1 [Source:HGNC Symbol;Acc:6250]
Mouse Orthologue:
Kcnh1
Mouse Description:
potassium voltage-gated channel, subfamily H (eag-related), member 1 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11625 | Nonsense | Available for shipment | Available now |
sa23088 | Nonsense | Available for shipment | Available now |
sa23089 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11625
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 |
---|---|---|---|---|---|
ENSDART00000029703 | Nonsense | 88 | 959 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 25526954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25666873 |
GRCz11 | 17 | 25685264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCACAGACAAGGACACAAGTGAAAAAGTTCGACTAACCTTCGAAAACTA[T/A]GAGATGAACTCGTTTGAGATCTTGATGTACAAGAAAAACAGTGAGGATCA
Long Flanking Sequence:
TGGCCATTTTCTCACCCCCAGGTTATTTTAAACCTCTATGACTTTCTTTCCTCTGTAGAACACAAAGGAGAAATTTAGTATTGTAACTCTTAGTCAAACTGAATAGTGACCTGGGGCTGTAAAGCTTCAAAAGGACTATAAAAACAGCCCATCTCACCATATGTTGTCAATGATGCTTTTGTATGGCTTCGGAAACTTGCAGAATAACACGTGATTGCTTTTAGCTATATTATAGAAGTTGATTTGAGTTTGATAGTGACTGGTGACCTTCAATCTTATAAAAAAGACAGCATGAACATTCTGCTAAAGTTCCCATTTTTGTGTGTTCCAAAATAATGCCATTTTGCCAATTTCTTTACAATATAATCCCAGTACATCTCAAAAACAGATCGAAAATGAACTGATTTGTGATTTGTTTGTCTTTTCTCTCTCAGCTTCATGTATGGAGAGCTCACAGACAAGGACACAAGTGAAAAAGTTCGACTAACCTTCGAAAACTA[T/A]GAGATGAACTCGTTTGAGATCTTGATGTACAAGAAAAACAGTGAGGATCACACACACACATGCACATGCACACACAGGATTGGAAACAGAGACACAGCAATCTTGTTGCATAAATCTGATATGCTAATATCTTTATGAATATGCATAAATGTGTAAAACAGAGCCAAGATGGTTTTTACTTCTTGGTTTTTACTGGCATGCCGACTTTCAGAGATTTAGGCAGTGTTAAATTGTGTGCTTCCAGGAACGCCGGTATGGTTTTTTGTGAAAATAGCCCCTATACGAAACGAACAGGAGAAGGTCGTACTCTTCCTGTGTACGTTTAGTGACATCACAGCATTCAAGCAACCAATAGAAGATGACTCCTCTAAAGGTAGGTGTATTTTAATGCAGGTAAATCAGCTCATTTGACTTTGAATGTTTAGTTATGTGTTTCTGTGTTCAGGCTGGGGGAAGTTTGCGCGTCTGACCAGGGCTTTGACCAGCAGTAGAGGGGTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23088
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029703 | Nonsense | 198 | 959 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 25531104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25671023 |
GRCz11 | 17 | 25689414 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACACGCAGGTTCTCCAGCTGGGCTCTGATATTCTGCCCCAGTACAAA[C/T]AAGAGACACCCAAAACCCCTCCTCACATCATCCTGCACTACTGTGCCTTC
Long Flanking Sequence:
AATTTTCTGTATTAATTATAAAATATAGGTGTTTTACCTGCATTTTGAATGTTATAATACACTGCATTGTGATTAGGTTTAACAGAAATCTCTGTAAACTTAATAAAATATTGTGCTATCAAAAAATTACCATAGGTTTTTTGTTTGTTTGTTTGTTTTTTCACCAGAATACCAATAGTCTCTATTCCGTTACACTCCATTAATTTTTCAATCATACATACAGTAATATAATGGCAACATACATTAATTCTATCAAGCTTTATTCAAAATGTCCATTAAAAACATATTTTAGTCAACGACAGGGCTTCATCTGTATCTATTAAACAGATGAGATGTTTTATAGCATGTGATTTTTCCCTGAGGTAAGACCCCTATAAGGAGCATTAGAGTCGAGACAGATCATTCCCCGTTGTCTCTGCTCAGATAAACGACCATCCGCTTTCTCTCTGTCTCACACGCAGGTTCTCCAGCTGGGCTCTGATATTCTGCCCCAGTACAAA[C/T]AAGAGACACCCAAAACCCCTCCTCACATCATCCTGCACTACTGTGCCTTCAAGACCACCTGGGACTGGGTGATCCTCATCCTCACCTTCTACACAGCCATCATGGTGCCCTACAACGTCTCCTTCAAGACCAAACAGAACAACGTCACCTGGCTAGTGGTGGACAGTATAGTGGATGTGATCTTTCTGGTGGACATTGTGCTGAATTTCCACACGACGTTTGTGGGCCCGGCCGGGGAAGTCATTTCAGACCCCAAACTGATTCGCATGAATTACTTGAAAACATGGTTTGTGATTGACCTGTTGTCCTGTCTGCCTTATGACGTCATCAACGCCTTTGAGAATGTGGATGAGGTCAGTACAACGCACTAAATCATTTATATATATATAAACATACACAAATGGGAAAAGGATTTATGATCAGTGATTAGATTGAAATGTGTGTGCATTGGTTTTGCCCAAGCTTTCTAGTGTGCTGAAGTTTGCAGTGTATTAAGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23089
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029703 | Essential Splice Site | 675 | 959 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 25587529)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25727448 |
GRCz11 | 17 | 25745839 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAACCACTTCTCCAGAAACCTCCTGCTTACGTACAACCTGCGCAAACGG[G/T]TGAGTGAAAAGCTGTCTACTATTCTCATTCACTTTCTGCTGATTTGCCTC
Long Flanking Sequence:
GCATATTTATATTTGTTTTAATAAAAACAAGTTTAGGTTTGTCCACCTGTCAGGTTTTGGAGATGTATGCGTCACTATATGGGGCATAAGAATAGGACGTGTGTTTGGATATAACTTCATAACTTATTTACAAAAGTAAAGGAGTAAAGAAAAAGAGAAAGAAAAGAGGCTGAAAGGAGGAGACTAAATCTTTATCTTTGGGCAGATTGTTTGTTTAAATGTTTTTTGCCTGTCAAGATCCTCCATTAATGTACCTATCATGCCTGTCAGTGTGTGTAATCATGCTTCTGTGTATCTCCACAGGTAAAGGTGATGTGTTTGGCGATGTGTTCTGGAAAGAAGTAACACTAGCTCAGGCGTGTGCTAACGTGAGAGCGCTAACATACTGTGACCTGCACGTCATCAAGCGGGACGCGCTTCAGAAAGTCCTGGAGTTCTACACGGCCTTCTCCAACCACTTCTCCAGAAACCTCCTGCTTACGTACAACCTGCGCAAACGG[G/T]TGAGTGAAAAGCTGTCTACTATTCTCATTCACTTTCTGCTGATTTGCCTCAGACCGCATGTGTAAGCAAAACTGTTCAGGCCCCACATGAATAGGATACAGCATTCAAACCTGCTCCACACAGTATGAGCACAGCTGGAAGAAGATTGAACTCATGGGATAATATGAATACAGCTCTCTAAAGCAGGTTATAAATACACTCACAAACTACATATAGTGACAAACCCTTTCTGTTTTTATATCGGAGCATATCAGTATTTCTTTTTTAGTCATTGTTATTTCATTACTTTAATTAACAATTCCAAATGAGTACTACTGTACTACAGAATGTGAGTGATTATCTGCTTGACCTTCGGACATAGGAGAAGATGGCATTACTTGATTGGCATTATTTTCTAAGGAGACACAAAAGAAGAAATTCTCGAATATTGTTTTGGTTCACACTGATATTGAATTTTCTGATCATCCAGTGGAAATCAATGGCAACTGATTCACAGAGGA
Associated Phenotype:
Not determined