ZMP
kcnh2
Ensembl ID:
ZFIN ID:
Description:
microtubule-associated protein 4 [Source:RefSeq peptide;Acc:NP_001036187]
Human Orthologue:
KCNH2
Human Description:
potassium voltage-gated channel, subfamily H (eag-related), member 2 [Source:HGNC Symbol;Acc:6251]
Mouse Orthologue:
Kcnh2
Mouse Description:
potassium voltage-gated channel, subfamily H (eag-related), member 2 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31277 | Essential Splice Site | Available for shipment | Available now |
sa38329 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14572 | Nonsense | Available for shipment | Available now |
sa19755 | Nonsense | Available for shipment | Available now |
sa32915 | Nonsense | Available for shipment | Available now |
sa19754 | Nonsense | Available for shipment | Available now |
sa32914 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31277
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024058 | Essential Splice Site | 26 | 1253 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 23783019)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24425476 |
GRCz11 | 2 | 24081127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCAGAACACCTTTCTGGACACCATCATTCGCAAATTCGAGGGTCAAAG[T/A]AAGTGAATGACTTTTATTTTAGTGAACGTGCATTGATTATGTTTTTAAAA
Long Flanking Sequence:
CTCACTGCCTCTCCATATTCACTATCAATCTATGCAATTTTAGTCAATTTTATTTTTAAACGCTCCCAAACACAGAGAGGGGCTGTTTCGCAGCGCGTCGGAGAAAGTGATTGAGTGAACTGGGACAGAAAGTTGATTTGCATCCATTTGCAAACAAAAAGGGAAGCAGGTGACGTGAGGTAATTGGAGAGACGGCTGATTTACTGAGCTCGAGGATGCGCGCACTGACAGATTTAACACGTAATCACTGGAGACTTTGAAGAGACGCGCTCTCGTGCTGCTTTTACATCGATGTGGTGTGAAGGTAAAGCTTGTGTACATGTGTAACACTTCGCGGTAGAGTCGATATATCGCTCTTATTCAAGTAAATACAAGCTGTCGAGGAACTTGCAGAACTTTCTTGCCCTGCTGTGGTAGGACAACATGCCTGTACGACGGGGACACGTTGCGCCTCAGAACACCTTTCTGGACACCATCATTCGCAAATTCGAGGGTCAAAG[T/A]AAGTGAATGACTTTTATTTTAGTGAACGTGCATTGATTATGTTTTTAAAACAGTTTCTAATGCTGACTATTGTTATTATTAAATATTTTGTTATTAATATTATTTTATTATCAATTGCCATTGAAAATTACTAATTGTCACTAATAATAATGTCGTTAATAACTTAATTTGAGTTAAACGTGTCAGAACAGCTAAGTAATCATTTACTTTTGCTATCTGAATATGTAAAAATAGTTAATTAAACATAATTTTACTTTTATTATTATTTTTAAAGTAGCCTATGTAAAACTAATTGATTTCAGATTTTCAGTAAGCTGCTGTTTCAGTAGATCTTTTAATGTAGCTAAAGCAGACACATTTATTCTGAACTGCAGCTCAATTTTGATTCTGCATAGATGTGGTTAATAAAATTTTTGCATTTCTATTTTTCTTGTACCTCAACAGATCGCAAATTCATCATCGCCAATGCTCGAGTTGAAAACTGTGCCATCATCTTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38329
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024058 | Essential Splice Site | 103 | 1253 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 23762905)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24445590 |
GRCz11 | 2 | 24101241 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGAATGTGTGACCGTTATTTTGAGAGATTTTTTTTCTCTCTTCACGCA[G/T]GTGTGTGTTTGCCTTGCCTTGTGGACGTGGTTCCTGTTAAGAACGAGGAC
Long Flanking Sequence:
GTTGTGAACCACCGCTGGCCATCAATACTGGCCCATCAGACTGGCACAGAAAGGGGCTGATTGGTTTGGCAGTGTAAGAGAGCAAAAACCACAGTGCCAATGTGAGACGGCTATCAAATGCCACCGTGAACAGTCAGGGCTCAGGACGTCTGCCAAACTGGTGATCGCAGACCTTAACACAGACCTCATTGATTCAAATAGCTACTGAAGTGGACAGCTTGTGAATAATTAAAAAACTATATATATATATATATATATATATATATATATATATATATATATAATTTTTTTTTTTTTTTCAGCTTGTGAATAATAATAATAAATACACTTGAATCATGACGTCAGACTATGTATATGGAACTGTTGTTGTATGCTGCTCTCTAGTGGTGACAAAGATGAAAGCTTTAATGGTTTTGTTTCTACCTGTATTGATGTTGTGTCTTTTTAGATTTTGAATGTGTGACCGTTATTTTGAGAGATTTTTTTTCTCTCTTCACGCA[G/T]GTGTGTGTTTGCCTTGCCTTGTGGACGTGGTTCCTGTTAAGAACGAGGACGGTTTAGTTATCATGTTTATCCTGAACTTTGAGCTGGCAGATCAGCAGGACAGACCCCTCGACAGCTCACCAGGCAGAGACATCAACAACAAAAACCCCATTCCGTGGCTCTCTAAAGGTATTTTAGGTTTATATTCAAGACTATCAGTTTTGTTTTTGTTTAATCAGTGGTATATGTAAAAAAATATTTATTAACAGTGTGCAAATTATACGTTGACGATCAGGGAGGGGGTCAATTCTTTTAGTAATAATAGTTTGTGTAATACATGCTTCAGTCATTTATGTATTTATTTAAATTATCAAATTTATTAATAAAACATATTTAAGTTTTTAGTGTTTGGAGGGTTGTTTACTGTATTTTGACTTACAGTAGCTTTCTTCTGATTATTTCAGATGTTAGTGTTGGCCAAACTATACAAACTATGCAGCTGATTTGACTTTACTTTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14572
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 |
---|---|---|---|---|---|
ENSDART00000024058 | Nonsense | 161 | 1253 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 23758856)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24449639 |
GRCz11 | 2 | 24105290 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTARYACAATACATTTATTTCTTACCCTTGGGTATTTCCTCAGCAAGA[C/T]GACGTCGTCTCCGGCTGCCACTGCCCTTGCTGCACTCTCTGAGTGGCAGK
Long Flanking Sequence:
TGTTGCACATCAGGGAATTTATTTGATAAATGTTTTTTTCCATCATAGCTTTTAATATGTTTTCTTATGTAAACTGTATCAGTCCCAATCTAGAACATACGTTATTAATCACATTTTAGTATTTTATGATCATCTTGGTTTTTATGTATTATCTCAAAATATTTTTTATAATATGTTAATGCAAATGTAGTGCACAGTCAACAATTTTTGTAAATTATATAGTATTTAACATTAATATGAACTGTATTTTAATGTAGGACAGTTATGCGGTCTGTATTGTGAAAATTACCATATTACAATTTTGTAGATATACAGCAATAGCAATGGTGCTGTCAATGTAAATACAGTATTTTTGCTCTAATTGATTTACTGTAAGTTACTGGTGAACTGCTGCAAGTAAGTTACTGTAGATTCTACAGGAAATTGTTAACAGTGTAGTGTGTAATTATGATCTAACACAATACATTTATTTCTTACCCTTGGGTATTTCCTCAGCAAGA[C/T]GACGTCGTCTCCGGCTGCCACTGCCCTTGCTGCACTCTCTGAGTGGCAGTAAACAGTCTCTGCATGAAGACACTGAAAAAGGCTTCATGCAGCCGATGCCTCATATGGGCCATGAGTCAGTAGCCCTGGACAAACTGCTCTCCCTACCTGAACGCTCAGCACTCGGAGGATCTCAGCTGTTGTTCTGGGAAGATAAGGCTCAGACTGAGTCTGAAAGTGAGCTGCGGCCATCAGAAGTGTCTCCTCCTCTGCCTCAGGGCTTCTCGCAGTCCTCCCCACGTCTGCACAACCTCACCTCAGAGGCGTCTCCGTCCAGTTGCAGCATGGCCCACAGCCGCTCCTGTGAGAGCCTGTGTGGCATGAGGCCCTCACCCTCCACCAATGACTTTAACTGGGACAGAAAACTGCCAGTCAGACCCAGTAGCACAGGTAAAATAGAAGGTTGAATGCGCTGACCAGATTTCTGAAATGTATTATCGAATTTAGTGGTAAAAATAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19755
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024058 | Nonsense | 267 | 1253 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 23758536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24449959 |
GRCz11 | 2 | 24105610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCCCCACGTCTGCACAACCTCACCTCAGAGGCGTCTCCGTCCAGTTG[C/A]AGCATGGCCCACAGCCGCTCCTGTGAGAGCCTGTGTGGCATGAGGCCCTC
Long Flanking Sequence:
GCAATGGTGCTGTCAATGTAAATACAGTATTTTTGCTCTAATTGATTTACTGTAAGTTACTGGTGAACTGCTGCAAGTAAGTTACTGTAGATTCTACAGGAAATTGTTAACAGTGTAGTGTGTAATTATGATCTAACACAATACATTTATTTCTTACCCTTGGGTATTTCCTCAGCAAGACGACGTCGTCTCCGGCTGCCACTGCCCTTGCTGCACTCTCTGAGTGGCAGTAAACAGTCTCTGCATGAAGACACTGAAAAAGGCTTCATGCAGCCGATGCCTCATATGGGCCATGAGTCAGTAGCCCTGGACAAACTGCTCTCCCTACCTGAACGCTCAGCACTCGGAGGATCTCAGCTGTTGTTCTGGGAAGATAAGGCTCAGACTGAGTCTGAAAGTGAGCTGCGGCCATCAGAAGTGTCTCCTCCTCTGCCTCAGGGCTTCTCGCAGTCCTCCCCACGTCTGCACAACCTCACCTCAGAGGCGTCTCCGTCCAGTTG[C/A]AGCATGGCCCACAGCCGCTCCTGTGAGAGCCTGTGTGGCATGAGGCCCTCACCCTCCACCAATGACTTTAACTGGGACAGAAAACTGCCAGTCAGACCCAGTAGCACAGGTAAAATAGAAGGTTGAATGCGCTGACCAGATTTCTGAAATGTATTATCGAATTTAGTGGTAAAAATAAAATTGAAATCTCTCTTATGATTATATATTTAAAATTTGGGGACAGCACATTTAGTATAGTTCTTATTTTTAATGAAAATATCTCTGGTTGAGGATGAGAAAAGAATAACAGGGAAATCTGATTACTCAGTGGTAGAAGAAAAAAACAGGTACACCTGGTCATACAGTGGTCATACAGTCAAAAATGAGCCAAAAGATCATGTCACAAGTGACATGCAAAGCAAATGTCTTTTATTGTCTTTTAACACGGCCATTTATTAAGGTCTGTGTAGATTTGATCATCAATTTTTGTAATCAATATATTGGAATGCCTGAGAAACAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32915
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024058 | Nonsense | 598 | 1253 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 23706458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24502037 |
GRCz11 | 2 | 24157688 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCGAATCGGTTGGCTTAATTCTTTGGGTGATCAGCTGGGAAAGCCATA[T/G]AATTCATCAGTACGTGGATCAGGACCCTCTATTAAAGATAAATATGTCAC
Long Flanking Sequence:
CAATACTTAAATCACTGTTAGTTCATAATAAAGTAAGATTTAGATTACATATTAATACATCATTATTCAAGTACCTTTATTGTTAAGTGTTATTGATAAATGGTTCACATTTTAGACCACATAGACTGCTATTGTGCCCACTCTGGAAACAGTTTTGAAAAAGTGATAAAAGAAATGCACCCTAGCAACTGTAATAACTGCTGCCGGTCAACTTACAACCTTTTAATTTTAAATTTTTTGATGTGTTAATAGACCACGACATCCACAACTCTGATTGGCCTGCTGAAAACAGCTCGGTTGCTGCGATTGGTGCGTGTGGCACGCAAACTTGACCGCTACTCTGAGTATGGAGCTGCTGTTCTCTTTCTGCTCATGTGTACCTTTGCTCTGATCGCCCATTGGCTGGCCTGCATCTGGTATGCGATTGGGAACGTGGAGAGAAGCGGCCCATCTCGAATCGGTTGGCTTAATTCTTTGGGTGATCAGCTGGGAAAGCCATA[T/G]AATTCATCAGTACGTGGATCAGGACCCTCTATTAAAGATAAATATGTCACTGCCCTGTACTTCACCTTCAGCAGCCTCACCAGCGTGGGCTTTGGAAACGTCTCCCCAAACACAAACTCAGAGAAGATCTTCTCCATCTGTGTGATGCTCATCGGAGGTTAGTGCTGCTAAGTGCTTATTCATATTCTAGAATGATGTCAGTGAGATTGTACAGTTATCAGTTGAACAATAATATTATAAAATACTTTCAGAACAAAGAATAGCTGTTTCTATATTAATACATTGAAGTTATTCATATACATTATAGTCTGACATTCAGTTTCACAGACACGATCCTTCAAAAATATTCTAATAGGCTGATTTAGAGCTCAACATTTAAATGTTGTGCTGTGTTAACTATTTTTAAGTAAATTGAATGACTAGAATGCTCAGAAGAACAGCATTAATTTTAAATTACATTATTATTATATATAATTTAGTGTATCCTTGTTGAAAAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19754
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 |
---|---|---|---|---|---|
ENSDART00000024058 | Nonsense | 1229 | 1253 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 23695967)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24512528 |
GRCz11 | 2 | 24168179 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAAGCTGTACAGAGTTTACATTTGGAGACCTCTGAGTGTTCAAGACGC[C/T]AATCGCTGCCAGTAAAACATCAGGTCGAAGATGATTGCTCAATGCAGAAA
Long Flanking Sequence:
ACACAGGACAATGTCCATGTCACTATTTTATTAAATAGCCTATTTTTTCAGATTTGAACATTCTTCAAAATAATAGAAATACATAAGTCGGGAAATTTTAATGAACATATTATACATTGTGCATTGAAGTTAACTCTACTTAATTTTGTGAACACACCATCTTTGATTTTTTTTTCTAGATACTTGATCCTCATGACTTTGCTGACAGTCCTATTAAGGCCAGTGAAAGTCTGTCAGGTGCAATGGAGCTCCAGCTCCTGGACTGTTCCTCACAGCCTCCCTCTGAGAATCCTTCTGGGGCTTATATGGGGAGATGGTCACGTAGCGTAAGCCACCACACAAACACCACTGGTGATCCTACAGCACACATCCATCTCCAACAAACAGCCATAGCTGATCAAGCTCATTACAGCTTTTTGGATGCAGAGCCTATTGGAACTCTTCGCCAACCACAAGCTGTACAGAGTTTACATTTGGAGACCTCTGAGTGTTCAAGACGC[C/T]AATCGCTGCCAGTAAAACATCAGGTCGAAGATGATTGCTCAATGCAGAAAAGACATCCCTCTGATCCTGGCTCTTAAGACAAACTTGTTCGGTATCTCAGTGGAAAACAATGCAAAGACCACCAACATGTTGGCATGGTGTTTAAAAGACTATTCAGGATCATATATAATTACCTCAGAAAAACGGTCAAGGATGCATCATTATTGTCCCTGTAGGTTTGTACATTTGTGTTAGCTGGTTTAACAATATTCATTGTTTTTACCTGCCTCATTATGAAAGTGTTCTCATTGTTTTGAGGTGTAAATGTAATGATTTGTATTAGCATATCAGCTTTTTTTTTACAATGTGGTTTTGTGTTGAATTGATTAGCCTATACTGTAGATTTTTTTTTAATAACTGAAACACTGGAAAGGCCAATCAGAGCAGGATTTATTAGAGTTCAAATGATCATTTGGAAACTTTAGCCCCTTTCATACATACAGACTTTTTCAGAAAATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32914
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 |
---|---|---|---|---|---|
ENSDART00000024058 | Nonsense | 1238 | 1253 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 23695940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24512555 |
GRCz11 | 2 | 24168206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCTCTGAGTGTTCAAGACGCCAATCGCTGCCAGTAAAACATCAGGTC[G/T]AAGATGATTGCTCAATGCAGAAAAGACATCCCTCTGATCCTGGCTCTTAA
Long Flanking Sequence:
TTATTAAATAGCCTATTTTTTCAGATTTGAACATTCTTCAAAATAATAGAAATACATAAGTCGGGAAATTTTAATGAACATATTATACATTGTGCATTGAAGTTAACTCTACTTAATTTTGTGAACACACCATCTTTGATTTTTTTTTCTAGATACTTGATCCTCATGACTTTGCTGACAGTCCTATTAAGGCCAGTGAAAGTCTGTCAGGTGCAATGGAGCTCCAGCTCCTGGACTGTTCCTCACAGCCTCCCTCTGAGAATCCTTCTGGGGCTTATATGGGGAGATGGTCACGTAGCGTAAGCCACCACACAAACACCACTGGTGATCCTACAGCACACATCCATCTCCAACAAACAGCCATAGCTGATCAAGCTCATTACAGCTTTTTGGATGCAGAGCCTATTGGAACTCTTCGCCAACCACAAGCTGTACAGAGTTTACATTTGGAGACCTCTGAGTGTTCAAGACGCCAATCGCTGCCAGTAAAACATCAGGTC[G/T]AAGATGATTGCTCAATGCAGAAAAGACATCCCTCTGATCCTGGCTCTTAAGACAAACTTGTTCGGTATCTCAGTGGAAAACAATGCAAAGACCACCAACATGTTGGCATGGTGTTTAAAAGACTATTCAGGATCATATATAATTACCTCAGAAAAACGGTCAAGGATGCATCATTATTGTCCCTGTAGGTTTGTACATTTGTGTTAGCTGGTTTAACAATATTCATTGTTTTTACCTGCCTCATTATGAAAGTGTTCTCATTGTTTTGAGGTGTAAATGTAATGATTTGTATTAGCATATCAGCTTTTTTTTTACAATGTGGTTTTGTGTTGAATTGATTAGCCTATACTGTAGATTTTTTTTTAATAACTGAAACACTGGAAAGGCCAATCAGAGCAGGATTTATTAGAGTTCAAATGATCATTTGGAAACTTTAGCCCCTTTCATACATACAGACTTTTTCAGAAAATTGTCAGTAATCATGTGTAAATCAAAGTAGT
Associated Phenotype:
Not determined