Busch Lab

ZMP

kcnh1

Ensembl ID:
ENSDARG00000024167
ZFIN ID:
ZDB-GENE-061226-1
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
sa42939 Nonsense Mutation detected in F1 DNA Not yet available
sa42940 Nonsense Mutation detected in F1 DNA Not yet available
sa23089 Essential Splice Site Available for shipment Available now
sa9197 Nonsense Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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:
sa42939
Status:
Mutation detected in F1 DNA
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
ENSDART00000029703 Nonsense 391 959 7 11
Genomic Location (Zv9):
Chromosome 17 (position 25546846)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 25686765
GRCz11 17 25705156
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGTCATTGATGAGGATCGTAACACAGTGCGTACGGACAGCTGGCTTTA[T/A]ATGCTTGCTGAGAGCATCGGGACACCCTACCGCTTCAATGCAAGCGGGAC
Long Flanking Sequence:
CTCTTTGTTCTGGCTGCTCAGGTGCTGTTTCAGCTCTCTGTATTGTTGATTTCAGAGGGCTGGCTTGGCAGACGCCTGTGCATATTTATACACACAAAGTATCTGTGTTAAAGGACAAAAGAAATGCACTTTTTTAGACTCAAGAAAAGACAAAAGTGCCTATAGAATTGCTTCAGCCTTTAATGTTTATAATTGGATGGATGGATGAAAACACTTTTGAACTATTACTCTGTTTAATTAATTAATTAATTAATCTCTTTTTCTCTCCCTCAGGGTATTAGTAGTTTGTTTAGTTCGCTGAAAGTGGTTCGGCTCTTGCGTCTTGGCCGAGTGGCTCGCAAACTGGATCACTACATCGAGTATGGAGCGGCGGTTTTGGTTCTGCTGGTTTGTGTGTTTGGGTTGGCGGCCCATTGGCTGGCCTGCATCTGGTACAGCATTGGAGACTATGAGGTCATTGATGAGGATCGTAACACAGTGCGTACGGACAGCTGGCTTTA[T/A]ATGCTTGCTGAGAGCATCGGGACACCCTACCGCTTCAATGCAAGCGGGACGGGAAGATGGGAAGGTGGACCCACTAAAGATACAGTCTACATCACGTCTCTGTACTTCACCATGACCAGCCTGACCAGTATTGGCTTTGGGAACATCGCTCCAACCACAGATGGGGAGAAGATCTTCGCCGTGGCCATGATGATGATCGGATGTGAGTTGAAAAGCTTTATGTACTTATAAACATCTGAGTGAAAATTACAGTGTTTTTCATATAGAAACAAGTTGTTGTTGCACATATAAGCATTTTGGGTTCAGTTGTACAGAATATCAAGCAATGCAGTGCTAAATTGAACTTGAAGTTCAGGGTTCAAGGAATAGAGTTGTCTCTACTCTAGTCCGGGAGACTTGGGATGTCTGAATATCACGTTTAACAACTGTAGTGAGATGCGATCCCGCTGTACATCCTGGATAAACTGTCCGACGTGCACTGCTCTCTGGAGCTCAGAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42940
Status:
Mutation detected in F1 DNA
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
ENSDART00000029703 Nonsense 554 959 9 11
Genomic Location (Zv9):
Chromosome 17 (position 25580142)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 25720061
GRCz11 17 25738452
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATCTGCGTGCACCTGAACAGGAAGGTCTTCAAGGAACATCCTGCTTTT[C/T]GATTGGCCAGTGACGGGTGTTTGCGGGCTCTGGCCATGGAGTTTCAGACC
Long Flanking Sequence:
ACCGCTTACCTCTGTATGGATTGCTTTTTAAAACACTGCGGTTGGGTTTAGAGAAGGGGGTGGGCAGATCAAATGGTGCTTTTTAAAATACTATTGGTTGGGTTTATGGAAGGGGGAGTGTGGGGGGATTGGTCGGTTGGTCAGTCAGTTAGTCAACAGTGGCCTATGGTGGATTTACGTGAGAACAGCAGGTGCGAATGGCACTCACGAGAGAAATTAGTGATCTGAAAATGTATACGTAGCAGCCTCTGGCAGATTCAAGAAAACAAAAACTGCAAAAAAACGTAGCTCCTGGGATGTATTTTGCTCTATCCAGAAATGTATATGGTGGTACGTCTTCAAAATGAGCCTAGGTGTTTTAAATAGAAAGGGTGTATCAAAATAACCACAAATCTGTAACATCTCTCTTTTAACAGGTTCTGCAGATCTGTCCCAAAGACATGCGAGCTGATATCTGCGTGCACCTGAACAGGAAGGTCTTCAAGGAACATCCTGCTTTT[C/T]GATTGGCCAGTGACGGGTGTTTGCGGGCTCTGGCCATGGAGTTTCAGACCATCCACTGCGCACCGGGGGATCTTATCTACCATGCGGGCGAAAGTGTGGACAGCCTCTGTTTTGTGGTGTCAGGGTCACTAGAGGTCATTCAAGATGATGAGGTGGTCGCCATTCTGGGTAAGAGCAAATCAGACTAGATTAGCAAGGCCACAGTTTTCTTCTCTGTATTTTCAAGATTTTAGTCTTAGTTTACGCATCATGACCTTTGACTACTCCGTTTTGATAATTTCTATTTTTTTAACGCCATAAGCCTGCTTGATCTTCTCCTCTACTTAATGACACCGACATCCCTCTGTCTTGGGTTTAGTCCCCTACGGGAGGATTATTTCCCTCCACAGAGCTTCTATGTGATCATATATCCTGAGTGTCAAACCCACTCCTCTATAGTGTCCTGTACATCTCTTTTGTTTCTTCTAATATTCTGAACCCTCTTTGATCAAGATGTCCAA
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.
Availability:
Order Allele From ZIRC
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

Mutation Details

Allele Name:
sa9197
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029703 Nonsense 905 959 11 11
Genomic Location (Zv9):
Chromosome 17 (position 25607362)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 25747281
GRCz11 17 25765672
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCCGAACACACGCTGCAAGCCTCGCTCTTGGAGCTCCGCACTGAACTC[A/T]AAGAAGAACTRTCGGCGCTCGGGAACCGAATGGTTGCGCTGGAGGCGCAG
Long Flanking Sequence:
GTCAAATCCACAATGAAGTCATCAGCCAAGATGTGATTGCCACCACAAGCATCGTTACTGTGACAGAGAGTCCAGCTACACCCATCCCATCCCACCTCATCAAAAACCGCACCCTAGGTCCATTCGACCAGGCGAAGCTTAGTGCCCCTGCCCCAAATGCCTCCCGCATGTCTGAACCACGTGCACGAGGATGGGCAAGGTTCAGGGAGAGCGTGGCAAAGCCTGAGAGCTGGGGAAACGTTCCTAAAGCTGAATCCATGGAGACTCTCCCTGAGCGGAGTAGCTCCGCAAAGACTTCAGAGCCTAGCGGACTCAAGAAGACAGACTCCTGTGATAGCGGCATTACCAAAAGTGACCTACGGCTGGATGAGGGTGGTATCCGCACCCCTGTGGACCGCAGTCCAGTCCAGCCCGATGGAAAATCTCCCCCAATCCCACCCATTCCAACCATTCCCGAACACACGCTGCAAGCCTCGCTCTTGGAGCTCCGCACTGAACTC[A/T]AAGAAGAACTGTCGGCGCTCGGGAACCGAATGGTTGCGCTGGAGGCGCAGGTCGCTGAGGTGCTGAGGTTGTTGCGAAACAGAAAGTCTCCAACCTCACCCATGTCGCTCTTCCAGATCTCACGGCCAACATCGCCAGACACAGACAAGGAGGACATGTTCCCTTGAAGAAAATGAGGTAAGAATATTTCTTCTTGAAAAGGGAAACTATTGAGACTTCCTCTGAGAAGAGAAGAAGAAATGGAACCACTTCTGACATCTGTGCCAGCAAAAAGCATGACAGACTTTGTCTGTGTGAGAAAGAGAGAATGAGTGAGGGAAAGGATGGAATAAGACACTGGAAAGGAGGAGAGGATGTCTTATCCCAAGGCAGAGCATCTGCGATACCAAAGTGATGGCGTGTTGGTTGTCACACGGAGACTCTGTGTGGAACTGCTCCCTGTTTTAGTCCTGCGAGGCTGACAGACAGTGAGAGCTCTTGCCGCAGGGCCCACTCTGACT
Associated Phenotype:
Not determined