ZMP
si:dkey-7m11.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens KCNQ5, potassium voltage-gated channel, KQT-like subfamily, membe
Human Orthologue:
KCNQ5
Human Description:
potassium voltage-gated channel, KQT-like subfamily, member 5 [Source:HGNC Symbol;Acc:6299]
Mouse Orthologue:
Kcnq5
Mouse Description:
potassium voltage-gated channel, subfamily Q, member 5 Gene [Source:MGI Symbol;Acc:MGI:1924937]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19519 | Nonsense | Available for shipment | Available now |
| sa39631 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19518 | Nonsense | Available for shipment | Available now |
| sa39630 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19519
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 |
|---|---|---|---|---|---|
| ENSDART00000085370 | Nonsense | 226 | 974 | 4 | 14 |
| ENSDART00000148069 | Nonsense | 109 | 538 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 1 (position 30227346)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 30367158 |
| GRCz11 | 1 | 31171089 |
KASP Assay ID:
2259-0715.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTTTTGCAACGTCTGCTCTGCGAAGCTTAAGATTTCTACAAATCCTG[C/T]GAATGGTACGCATGGACCGCCGCGGAGGAACTTGGAAGCTTCTGGGATCT
Long Flanking Sequence:
GGCCTTCAAGTCACAAAGGTTGAGGTCCATTAATTAATGGATGCTTTGTTCAATGGGATTTACAGCGTAATTATTATAAGAACAGGTCACCTAGGAACTCAGTTGCAACTTTCAGACTGAACAGGAAAAAAATGTAGATATTGTAGAGGTTGAATATATTATTCTGTAACAGTCTCAGTTTTTTTTTTTAAATGTTAGCATTATCTTGATAATCTGAAGGGTGAGATTTATTTTGCAACAACATTCCTTGTGAAAAAAGCAAACATGTGACCTGTCAGCATCAAATTGTCTATGTAGCAAAAATATATAATTTTGAATTTTACATCTGTAATCATGTTAGGACACTTATGACTCATGTAAAATGTATTTTTTTCTGTTTGTTTTTCCAATCATTAGACATAATAGTGCTGATTGCCTCAGTTGCTGTGGTTTCGGCGGGGAGTCAAAGCAACATTTTTGCAACGTCTGCTCTGCGAAGCTTAAGATTTCTACAAATCCTG[C/T]GAATGGTACGCATGGACCGCCGCGGAGGAACTTGGAAGCTTCTGGGATCTGTAGTTTATGCACACAGCAAGGTAACTTGATTTTTGACAAATTGTCATCTAAAATTATTTAAAAGGTTGTCTGTAAAATGAGTAGACCAATTCTAAAAGCTCAATTTGTTTTTGCAGTGATAGTCTGTGTCAAACAGCCATGTCTGAAAGTACTTTCTGTTCTTTTGTAAATATCTTCCTCGTCTGCCGATCTTCTCTAAACGTCCTCAATATCTGCTTCTCTGTCTGATAGGAACTGGTCACTGCCTGGTATATTGGGTTCCTTGTGCTCATCTTTTCCTCTTTCCTGGTTTATCTGGTGGAAAAGGAATTCAATAAAGACTTTGCCACCTATGCTGATGCATTATGGTGGGGCACGGTGAGTCTTCACATTGCACATTTCTACATAATGGTACATTCTATCAGAGTCCAGGTAATAGTCTGGTCTATACTGAGCTTTACAAAACAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39631
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085370 | Essential Splice Site | 249 | 974 | 4 | 14 |
| ENSDART00000148069 | Essential Splice Site | 132 | 538 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 1 (position 30227273)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 30367085 |
| GRCz11 | 1 | 31171016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGAGGAACTTGGAAGCTTCTGGGATCTGTAGTTTATGCACACAGCAAGG[T/C]AACTTGATTTTTGACAAATTGTCATCTAAAATTATTTAAAAGGTTGTCTG
Long Flanking Sequence:
TTATAAGAACAGGTCACCTAGGAACTCAGTTGCAACTTTCAGACTGAACAGGAAAAAAATGTAGATATTGTAGAGGTTGAATATATTATTCTGTAACAGTCTCAGTTTTTTTTTTTAAATGTTAGCATTATCTTGATAATCTGAAGGGTGAGATTTATTTTGCAACAACATTCCTTGTGAAAAAAGCAAACATGTGACCTGTCAGCATCAAATTGTCTATGTAGCAAAAATATATAATTTTGAATTTTACATCTGTAATCATGTTAGGACACTTATGACTCATGTAAAATGTATTTTTTTCTGTTTGTTTTTCCAATCATTAGACATAATAGTGCTGATTGCCTCAGTTGCTGTGGTTTCGGCGGGGAGTCAAAGCAACATTTTTGCAACGTCTGCTCTGCGAAGCTTAAGATTTCTACAAATCCTGCGAATGGTACGCATGGACCGCCGCGGAGGAACTTGGAAGCTTCTGGGATCTGTAGTTTATGCACACAGCAAGG[T/C]AACTTGATTTTTGACAAATTGTCATCTAAAATTATTTAAAAGGTTGTCTGTAAAATGAGTAGACCAATTCTAAAAGCTCAATTTGTTTTTGCAGTGATAGTCTGTGTCAAACAGCCATGTCTGAAAGTACTTTCTGTTCTTTTGTAAATATCTTCCTCGTCTGCCGATCTTCTCTAAACGTCCTCAATATCTGCTTCTCTGTCTGATAGGAACTGGTCACTGCCTGGTATATTGGGTTCCTTGTGCTCATCTTTTCCTCTTTCCTGGTTTATCTGGTGGAAAAGGAATTCAATAAAGACTTTGCCACCTATGCTGATGCATTATGGTGGGGCACGGTGAGTCTTCACATTGCACATTTCTACATAATGGTACATTCTATCAGAGTCCAGGTAATAGTCTGGTCTATACTGAGCTTTACAAAACAACTCATTCATATTTAATGTGGTGCCAGATTCATGTTCTAGCACCTCTGTGCCTCTTGTACAGTTATTATTCTGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19518
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 |
|---|---|---|---|---|---|
| ENSDART00000085370 | Nonsense | 331 | 974 | 7 | 14 |
| ENSDART00000148069 | Nonsense | 214 | 538 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 1 (position 30222545)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 30362357 |
| GRCz11 | 1 | 31166288 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGTTGTCCATTTTTCATGATATGGTTCTTTTTCACTTGCAGGGTATTT[T/A]GGGTTCAGGTTTTGCCTTGAAGGTTCAAGAGCAGCACAGACAGAAGCACT
Long Flanking Sequence:
GGTAAACCTTACACACACACACACACCAAAAAGCATTCTGACATTGTGCCTAGTGTCTCTACACTAATTACAGTATTAATTCAGTGCTTGTGTTTATTGTCACTCCTCCAGATACAACACTGATAATAAAAATGAAAAAATAAATAAATCAATTACAAATCATTTGCATAATTGAAATTGTTTCCAATGTTTTTCTTGGTTTCCAGGCTGCTCTGCACAATCAAATCTTATTATTAGCATATTATTTTTTTTCATAAAGCCGAAAAATGATCTATTTGTGAGGCACGTTGCTCGCAGTGCCACCAACAGAGAGTGTGTTTAGAGAATACAAATGTAGTGTTCATACAACACTACAAAACGAATGAGTAAACAGAGAGTACCAATACCAAGTGAAACAAGTATATATATTTTTAAAATTCAGACAGTAAATATACATTCAAAACCAAGTGCAGTGTTGTCCATTTTTCATGATATGGTTCTTTTTCACTTGCAGGGTATTT[T/A]GGGTTCAGGTTTTGCCTTGAAGGTTCAAGAGCAGCACAGACAGAAGCACTTCGAGAAGAGAAGGAACCCTGCTGCCTGCCTCATACAGGTCAGACACAAGAGCTATTAATCTGCCTTCATATTGAGTGATATTACACAATCTGGTACAATAAAACTTGGTTTATAGTGTCATAAAGACTCATGTCCCTTTTTAGAGTACTGTTTGGTCCTGTGTCTTTTTATGTAACTGTTATTCATGTCTGAATGCACCACAATGTTTGTCTGTGTTGCCTGATGAATCTTTTATGACTATCTGAGACAGCAGATAGTCCTAGCTAAAAACTTGCTCCAAATATGATTCACTTTACTGCAAAAAGACTTTGTTTGCTTAGACATCCAGTGTTTCACTGGTTTTAAAGGGTCATGATAATATTCTTTAGGACTAGTTAGTTCTTGTAAGAAAGAAGAGAGACAAATAACAAAGAACAGCAACAACTGGTTTTATGATTATGTATTGTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39630
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 |
|---|---|---|---|---|---|
| ENSDART00000085370 | Nonsense | 681 | 974 | 14 | 14 |
| ENSDART00000148069 | None | None | 538 | None | 13 |
Genomic Location (Zv9):
Chromosome 1 (position 30192820)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 30332632 |
| GRCz11 | 1 | 31136563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAGGGCCCTCCAGCTAATATTAGCCCCCAATGAACTCATGAACCTCAAC[C/T]AGAACAACTCCACAACATCTTCCCCAGGACTCAACCCAGCGTCCGCCTCC
Long Flanking Sequence:
TGGCAGCGTGTGGGTTAGTCTGTCGGTGGCTTTATTTATTTTTGGAAACTTAAAAAAGGACACTACCCTCATATTATACAGCATGAAAGAGTTAGGATAAAATTTAAAACTACTCCGTCTGTGTTCATCTGATGGAAGAAAGTTATATACACCAAGGTTGGCATAAGGTTGAGTAAACTATTGGGCAAAGTTATTACTTTAAAGACTCATGCAACACTAAGTCAAAAATATTTCTGTGTTCTTCTCTATAGGTTCAATCTATTGAGTCTAAGCTGGACTCGTTGCTGGACATCTACCGGCAGGTTCTGCAGAAGGGTTCTTCCACAGCCCTCACGTTTTCCTCTCTTCCTCCTTTTGGTTTGGAGGAGAATTCAGATTATCAGAGCACCGTCCTTAGTAAGGATCTCTCTTGTGCGTCGCAGGTCAGCCAGTCCATCTGTGGCAATCACCCTAGGGCCCTCCAGCTAATATTAGCCCCCAATGAACTCATGAACCTCAAC[C/T]AGAACAACTCCACAACATCTTCCCCAGGACTCAACCCAGCGTCCGCCTCCCCTTTTAACCTGTCGACCTTCCAGGTTCCTTCAACTCCATCACTGGAGTGTCCGTCAGCACAAGGCAGTCCATCTCAGATCCTAAACGCCAACAGTTTTCACTGCTCTATAGGCCACTTTCCAAGCGTGGGTCAACCACCTCCACCTCTCTCATCCACAACCACTTCAAAATATCAACTTTCCACAGTTCCTTCACAAGCAGGCCATGCTCGCAGTATGGGACCCACTAGGTCGGATCCCGCAGACTACGCCAAGTCTTGCTTCAGAGGAGTTGGGATAGACCTTGGACTCAACTCTAGTATGATCTGCAAGCTTCAGCAGAAAAACAGACCCAGTGCTAAAGAGGACAGTTCTTGGAGAAGACATATAAGTCTGGATTCAGAGGTGGAGATGGACCCCCTTGCTCCAGTCTCACCTCTTGCCCCAGTTCAAGGCCAGTGCAGTGGGGAC
Associated Phenotype:
Not determined