ZMP
KCNH7 (2 of 2)
Ensembl ID:
Description:
potassium voltage-gated channel, subfamily H (eag-related), member 7 [Source:HGNC Symbol;Acc:18863]
Human Orthologue:
KCNH7
Human Description:
potassium voltage-gated channel, subfamily H (eag-related), member 7 [Source:HGNC Symbol;Acc:18863]
Mouse Orthologue:
Kcnh7
Mouse Description:
potassium voltage-gated channel, subfamily H (eag-related), member 7 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15943 | Nonsense | Available for shipment | Available now |
sa7578 | Missense | Mutation detected in F1 DNA | Not yet available |
sa6067 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31499 | Nonsense | Available for shipment | Available now |
sa38540 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15943
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 |
---|---|---|---|---|---|
ENSDART00000090874 | Nonsense | 152 | 1208 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 10401346)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10254972 |
GRCz11 | 6 | 10490399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGCAGCATGGATTCATTAGACCGACTCAAYCACACCTCCCCAGCCAGA[C/T]AAGAACAAAGTGAGGATATTTCTTTTTATGATTCCCTCTCTTTAAAGAAA
Long Flanking Sequence:
TCCGTTGTGCTTTTCTCAAGGGTCGTCTTGCCCTTTGGTTGCCATGGCGACCCCCTTTCTCGCCTGTCAGGAATGAATTCTGAACCTGTCAAACTGAATGAGCGTCAACATCTACACACAAAAACTGCGTGTTTGTTTGTGTCACGAAGCACGAAGAGTGTAACCTGCTCTCCACTGTTACCCTCTGCCTCTATTTATTTATCAATTAACCAGATGATTATTATAAATCTCAATTAAGCAGAATTAATCAGACGTCAGTGGTCATTTAAAGATGCTCACTTAATGCTTAGATTTGTTTGGCTGTCTAAACTAATAGGTGAACTAAAAGTGTTTTTTTTCTCTTTTCACCTGCAGGATCAGACTTTCTGTGTGCGACACACATCATTCCAGTGAAGAACCAGGAGGGTGTTGTTATGATGTTCATCTTGAGCTTCGATTATGTGCTGAAGGAGGGCAGCATGGATTCATTAGACCGACTCAACCACACCTCCCCAGCCAGA[C/T]AAGAACAAAGTGAGGATATTTCTTTTTATGATTCCCTCTCTTTAAAGAAATGCTCCACTTTTTTCGAAAATGGGCTCATTTTACAACTGCCCTGGAATTAAACATTTTGAGTTTTACCATTTTTGAATTAATTCGGCCGATTTTCAGGTCTGGCGGGAGAAGTTAGCTTAGCTTAGCAATGTGCATGGGACGATAACCAGCTTCAAGGTTTACCACAGCTTGGAAAAGTCAAGGTTTTAAAACTGCATACTGTTCCTATGGTATTTTTAAGTAGTTTTTTAAATGTATTTTCATTTATTGGACTATATATTAAGTTTAGTTTTTATTTATTTTTTGATTATTTTGTTTTACAGTATCTCCAGCAGCACAGTAGCATCTACATCAAAAGCTACAGGTCAGCTCACGATTCAGGGAACATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCCGGGGTTGCCACAGAGGAATGAACGATTTTAGTGAAGTTTATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7578
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 > C
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090874 | Missense | 334 | 1208 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 10433304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10286930 |
GRCz11 | 6 | 10522357 |
KASP Assay ID:
554-4250.1 (used for ordering genotyping assays)
KASP Sequence:
ATTTAATCAGATCAAGTCCAGCCTCYTGGGCTCCACGTCTGACTCAAACC[T/C]GACCAAGTACAGCACCATCAACAAGATCCCACTCATCACTCTCAACTTCT
Long Flanking Sequence:
AAGAGAATGCATTGTTTAGATTCTTGTAGCATTTTTTTTTTCAATATATAAGATTGTTTGGACCATTTCAGTTAAGTGACCTGTTTGCATCAATGAGATGGTTCAAGATTCTATCTGACCTCACTGTCTTTTTTTTCCTTAAGTTAAATCATTCTCTGCTCCCCCTCCCTCTCTTTCGCTCTCTTCTCATTGGCTAGTGTCGCGCTCTTGGATGGCTGGGGGTATGGCTAGAGCTTCACTTCTTTCATTTAAACATTGGCATGTTTCTGTCGTCTGTGCGTCTGCTGTTTTTGTATCTTGTGTTTGCAGTTGACTTACATGTTGTTGTTGTTGTTGTTGACCACTGTTAATCTGGAAAATCTCAGTGTTGATGTCAGTTTTAAAGTGATTCCTGCTACATTAAACAGAGTTGCACCTTGCTTATGATTTGTGTGTTTATTCTTTAGGTCCATTTAATCAGATCAAGTCCAGCCTCCTGGGCTCCACGTCTGACTCAAACC[T/C]GACCAAGTACAGCACCATCAACAAGATCCCACTCATCACTCTCAACTTCTCAGAAACCAACCATGACAAGCGGCCATCATCTCCACATTCCTCCGAGAAAACCATCATCGCACCAAAGGTCAAGGATCGAACACATAACGTCACAGACAAAGTCACACAGGTGAGAGATGAACATTAAATCAGGTAAACACTCATCTGTTACTATAAATGCACCTAAAAATGGAGTAAGCAATGTGATTTCACAAAAAGTCATTTGTTACGACAGAATGGTTAATGGTAAATAAACTAGTTTAAAGTTATAAGAATCAGAGCTGTCATCCTCAACAACACTGATCCATTTATTTGTCATAAATCATCACTGATTATTGTAGTAACCCTAAAGGGAACCATGTCATTGTGGCAGGAATTTTTCATTTAATTCTTTTGTTTTGTTTTATTGATGTATTGAAATGCTTTGGGTGAATGACAATACTCAATAAATGTGCTATATAAATGTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6067
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090874 | Nonsense | 581 | 1208 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 10451178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10304804 |
GRCz11 | 6 | 10540231 |
KASP Assay ID:
554-3957.1 (used for ordering genotyping assays)
KASP Sequence:
CTCCTCATGTGTATCTTTGCACTGATTGCCCATTGGTTGGCTTGCATATG[G/A]TATGCGATCGGCAATGTGGAGAGGCTCTATCTGGACCACACCATTGGCTG
Long Flanking Sequence:
CAGACGCAGCCCATTTTTTTAAACAAACCAACTGGACAGATGAAGAACAAACTGGTGGATAAAGAATGAGTAAGTGAGTGAGTGGTAATGTCAGAGGACTGAGAGTGTTGATGAAACAGGTAGGTGTTCAGTCGTTTAATAAAAATTTGATTTGAATTCTTAAAAAGCTTCTTAAAAATTGGAAAAAAAAATGAAACTCAGCAATGTCTGAATAAAGATTCTTACTGTAAATCAATGCATAGCGGACTCTAGATTTATTGTAATTAATTAGTTGTGATTTTATCTGAATGCATTGCTTTATTTATGCTTGCATGATTATGTGTGTTCTTCTCACCCTCTCTTTAGACCACTACTCTGATTGGCCTGTTGAAGACTGCTCGACTGCTCCGATTGGTCCGTGTGGCTCGCAAGCTGGATCGATACTCCGAGTATGGGGCGGCTGTTCTAATGCTCCTCATGTGTATCTTTGCACTGATTGCCCATTGGTTGGCTTGCATATG[G/A]TATGCGATCGGCAATGTGGAGAGGCTCTATCTGGACCACACCATTGGCTGGTTGGATAATTTGGGCATATCCATCGGCAAGCAGTACAACATAAGTGATGATGCCTCAGGCCCCTCTATCAGGGACAAGTACGTGACAGCGCTGTATTTCACATTCAGCAGTCTGACCAGTGTGGGCTTCGGAAATGTATCACCAAATACAAACTCAGAGAAGATCTTCTCCATCTGTGTCATGCTCATTGGCTGTGAGTATTATTGAGATCACTGTTCATGGACGATCCCCCGCTCTGCATATTTTCCATCCTCCTTAACCAAACACACCTGATTCAAATCATTGGCTAATTAGCAGAGACTAAAAGACTGTAATGGGTGTGACAGATTATTGAGACATCCAAAACATGCAGTGCTGGTGGTCCTCCAGGAACATGGTTGAGAAACACTGCACTATACTATCTTCACACACGTGTATAGCTATGTTAGTGAGGGCTTTCCGTACACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31499
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 |
---|---|---|---|---|---|
ENSDART00000090874 | Nonsense | 798 | 1208 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 10458495)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10312121 |
GRCz11 | 6 | 10547548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTCTGGTGCATGGTGGGGATGTTCTCACTGCCCTCTACTTTCTCGCC[A/T]GAGGGTCTATCGAGATCCTCAGAGATGACATTGTGGTGGCCATCTTGGGT
Long Flanking Sequence:
AGAAAGCATAATTGGCAGCTGCATTTTCCTCTGCTTAATGTGCCGTATATCATTTAATATGAAGCCAAAACAAATCAAAGCCAAAAACAATGCAAAGCAGTCGAAACAAAGGGTCCCGGATGCATTTGTGTTTTGCTTCATCTTTTATGTATTTGCAGTTGAGGGAGACGGGGCTATATTAGCATTGTATAATCTGGGCTGGTAAAAATCTGCAACCGTTCTGCCCTTCATCTCCTCTTGTCTATTGGGAACACTCTTTCTGTTCTGTCCTTTTCTGTCTCTTCCTCTCTCTGCAGGTATTGAAGGGTTTTCCAGAGTGCCTGCAGGCTGATATCTGTCTCCACCTGAATAAAACGTTGCTCCAGAGCTGCAAGGCCTTTCGTGGAGCGACCAAAGGTTGCCTTCGGGCACTGGCGATGCGCTTTAAGACCACCCATGCCCCACCGGGTGACACTCTGGTGCATGGTGGGGATGTTCTCACTGCCCTCTACTTTCTCGCC[A/T]GAGGGTCTATCGAGATCCTCAGAGATGACATTGTGGTGGCCATCTTGGGTGAGCATTAAACAATTAATAAAAACTTTTTTTTTTTTAAAGGCCCATGCATACCAAGACGATTTCTGCTCACGCTTTTTGCTGATGTTTAATGCCTTGTGACTAAGCAAAGCCAACCAATCTGAGCACACACACCCAACGCACAAAATGGCTGTCATTAAAGCTTTATTAAAAAAAAAAAACTTTTAGCAATAATAAATGCTTAGCCAATGCAAATAGAACTTTTGTTCATCCGTCTGGAACTTGAAGCTTCTGAAATTACATTAAACATGACTTGGTTGCACTCAAGACAAGGTGAAGAAAGTTTATTTATACAGTACATTTCAAACACAAAGGTAATTCAAAGATTAAAGCTGCAAGCAGCGATAAAAGGGACCTCGCAACTGGGCTCACCGCCTCATGGTGGCCTTAGGATGTGGATTAGGAAGCAGATCAGACAGCGCATGCCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38540
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090874 | Nonsense | 805 | 1208 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 10458516)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 10312142 |
GRCz11 | 6 | 10547569 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTCTCACTGCCCTCTACTTTCTCGCCAGAGGGTCTATCGAGATCCTC[A/T]GAGATGACATTGTGGTGGCCATCTTGGGTGAGCATTAAACAATTAATAAA
Long Flanking Sequence:
CATTTTCCTCTGCTTAATGTGCCGTATATCATTTAATATGAAGCCAAAACAAATCAAAGCCAAAAACAATGCAAAGCAGTCGAAACAAAGGGTCCCGGATGCATTTGTGTTTTGCTTCATCTTTTATGTATTTGCAGTTGAGGGAGACGGGGCTATATTAGCATTGTATAATCTGGGCTGGTAAAAATCTGCAACCGTTCTGCCCTTCATCTCCTCTTGTCTATTGGGAACACTCTTTCTGTTCTGTCCTTTTCTGTCTCTTCCTCTCTCTGCAGGTATTGAAGGGTTTTCCAGAGTGCCTGCAGGCTGATATCTGTCTCCACCTGAATAAAACGTTGCTCCAGAGCTGCAAGGCCTTTCGTGGAGCGACCAAAGGTTGCCTTCGGGCACTGGCGATGCGCTTTAAGACCACCCATGCCCCACCGGGTGACACTCTGGTGCATGGTGGGGATGTTCTCACTGCCCTCTACTTTCTCGCCAGAGGGTCTATCGAGATCCTC[A/T]GAGATGACATTGTGGTGGCCATCTTGGGTGAGCATTAAACAATTAATAAAAACTTTTTTTTTTTTAAAGGCCCATGCATACCAAGACGATTTCTGCTCACGCTTTTTGCTGATGTTTAATGCCTTGTGACTAAGCAAAGCCAACCAATCTGAGCACACACACCCAACGCACAAAATGGCTGTCATTAAAGCTTTATTAAAAAAAAAAAACTTTTAGCAATAATAAATGCTTAGCCAATGCAAATAGAACTTTTGTTCATCCGTCTGGAACTTGAAGCTTCTGAAATTACATTAAACATGACTTGGTTGCACTCAAGACAAGGTGAAGAAAGTTTATTTATACAGTACATTTCAAACACAAAGGTAATTCAAAGATTAAAGCTGCAAGCAGCGATAAAAGGGACCTCGCAACTGGGCTCACCGCCTCATGGTGGCCTTAGGATGTGGATTAGGAAGCAGATCAGACAGCGCATGCCTGAGTTATAACAACTTCCTGTTTCT
Associated Phenotype:
Not determined