ZMP
si:dkey-29l6.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate potassium voltage-gated channel, KQT-like subfamily, member 5 (K
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 |
|---|---|---|---|
| sa9563 | Nonsense | Available for shipment | Available now |
| sa11293 | Nonsense | Available for shipment | Available now |
| sa22313 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9563
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 |
|---|---|---|---|---|---|
| ENSDART00000102232 | Nonsense | 100 | 975 | 1 | 15 |
| ENSDART00000139904 | Nonsense | 100 | 929 | 1 | 13 |
| ENSDART00000146230 | None | None | 173 | None | 3 |
| ENSDART00000102232 | Nonsense | 100 | 975 | 1 | 15 |
| ENSDART00000139904 | Nonsense | 100 | 929 | 1 | 13 |
| ENSDART00000146230 | None | None | 173 | None | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 27844408)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 27490068 |
| GRCz11 | 13 | 27620518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAACGCRCGCTACAGGARGCTCCAGAACTACCTCTACARTGTCCTGGAG[C/T]GACCGCGAGCCTGGGCATTCGTTTACCATGYCTTTGTGTAAGTAAAAATG
Long Flanking Sequence:
TTCATAGCTGATCTGCAAATGAGCTTGATGCCTGCACTTGTCAGTAGGTGATCCTGTTATTTACATGTAATGCTAAAGAAAAAAGAAGAACAATAAAACACTCAATGTTTTTACACAGGGAACTGTGAATCTCGTGTACAGCTTCTTTGTATGTGCGCACCGCTGGTGCCAGACGCGCGTTTCCAGCCTGCGCTGGTGATGCGATGCCCCGCAACCACAGCGGCGATGAGGGCGGTGCTGGTCTCTGGATGAAGACCTCGCAGCACTATGGCATGAAAGATGTTGAAGCCGGTCGCGGGACGATGAACAACGCGACCAGGAATGCCGACAGTCTACTGTCGGCGCCGGGTACAACAGGTGCAGGAGGCTCCGAGAACCAGAGGAGAAATCAGGGCGCCCGTCTAAGCCTGCTGGGGAAGCCGCTCGCATACAGCGCGCAGAGCGGCCGGAGAAACGCGCGCTACAGGAAGCTCCAGAACTACCTCTACAATGTCCTGGAG[C/T]GACCGCGAGCCTGGGCATTCGTTTACCATGCCTTTGTGTAAGTAAAAATGTCTTTACTCTTTTATTCATGACGCCATGGATAATCACAGCTGGAGTTCACCTGTTACTTAAAGTTATTCTATACACTGTCAATGGCATCCATACACTTTGCTTGTCTTAATTGTGTTTAAAATGCTTAGATTAATATTATTTTTTAAGATCTTTTGATTTATGGAGGAGGTAAAGGGAGTTTGAGCACTGTAATCTAAATGTTGTTAGTCACATGTCAGTCTTGTTGTTATGAAATTTTATAGTTCAATAGAATTTACGAGTTGGGTTGTATAAATGCTGATGCATTTTGATTCTTTTCAGTAACTCATGTTTGATGCCATATTATTTAAAACCTTAAATGTTGTCAAACAATGCATTTTTTAGACAGTAAAATATATCTGATCGCTGATTTACCATCAAGCAGTGGCCTTTAGTAAACTTGGCCGTTTGTCATTTTAACACACCAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11293
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 |
|---|---|---|---|---|---|
| ENSDART00000102232 | Nonsense | 100 | 975 | 1 | 15 |
| ENSDART00000139904 | Nonsense | 100 | 929 | 1 | 13 |
| ENSDART00000146230 | None | None | 173 | None | 3 |
| ENSDART00000102232 | Nonsense | 100 | 975 | 1 | 15 |
| ENSDART00000139904 | Nonsense | 100 | 929 | 1 | 13 |
| ENSDART00000146230 | None | None | 173 | None | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 27844408)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 27490068 |
| GRCz11 | 13 | 27620518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAACGCRCGCTACAGGARGCTCCAGAACTACCTCTACARTGTCCTGGAG[C/T]GACCGCGAGCCTGGGCATTCGTTTACCATGYCTTTGTGTAAGTAAAAATG
Long Flanking Sequence:
TTCATAGCTGATCTGCAAATGAGCTTGATGCCTGCACTTGTCAGTAGGTGATCCTGTTATTTACATGTAATGCTAAAGAAAAAAGAAGAACAATAAAACACTCAATGTTTTTACACAGGGAACTGTGAATCTCGTGTACAGCTTCTTTGTATGTGCGCACCGCTGGTGCCAGACGCGCGTTTCCAGCCTGCGCTGGTGATGCGATGCCCCGCAACCACAGCGGCGATGAGGGCGGTGCTGGTCTCTGGATGAAGACCTCGCAGCACTATGGCATGAAAGATGTTGAAGCCGGTCGCGGGACGATGAACAACGCGACCAGGAATGCCGACAGTCTACTGTCGGCGCCGGGTACAACAGGTGCAGGAGGCTCCGAGAACCAGAGGAGAAATCAGGGCGCCCGTCTAAGCCTGCTGGGGAAGCCGCTCGCATACAGCGCGCAGAGCGGCCGGAGAAACGCGCGCTACAGGAAGCTCCAGAACTACCTCTACAATGTCCTGGAG[C/T]GACCGCGAGCCTGGGCATTCGTTTACCATGCCTTTGTGTAAGTAAAAATGTCTTTACTCTTTTATTCATGACGCCATGGATAATCACAGCTGGAGTTCACCTGTTACTTAAAGTTATTCTATACACTGTCAATGGCATCCATACACTTTGCTTGTCTTAATTGTGTTTAAAATGCTTAGATTAATATTATTTTTTAAGATCTTTTGATTTATGGAGGAGGTAAAGGGAGTTTGAGCACTGTAATCTAAATGTTGTTAGTCACATGTCAGTCTTGTTGTTATGAAATTTTATAGTTCAATAGAATTTACGAGTTGGGTTGTATAAATGCTGATGCATTTTGATTCTTTTCAGTAACTCATGTTTGATGCCATATTATTTAAAACCTTAAATGTTGTCAAACAATGCATTTTTTAGACAGTAAAATATATCTGATCGCTGATTTACCATCAAGCAGTGGCCTTTAGTAAACTTGGCCGTTTGTCATTTTAACACACCAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22313
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 |
|---|---|---|---|---|---|
| ENSDART00000102232 | Nonsense | 173 | 975 | 3 | 15 |
| ENSDART00000139904 | Nonsense | 173 | 929 | 3 | 13 |
| ENSDART00000146230 | None | None | 173 | None | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 27661356)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 27307016 |
| GRCz11 | 13 | 27437466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGCATCTGGTCTGCTGGATGCTGCTGCCGGTACAGGGGATGGCAAGGA[C/T]GACTGCGCTTCGCTAGAAAACCATTCTGTGTGATAGGTAAGATAAAAATA
Long Flanking Sequence:
TTATGATACAAACAGGTATAATGATATGAGCTCGATTTTTATTGGAAATGTCTTGCTTTGCTTTTGTGGAGCAGAAAACAAAGTCTTCTCAAATTACCAACAGCTCAAATCAAACTCTTCCAGGCCTAAGCTGGAACAATATCACAGTAAAATCAAGCTCACTTTATGGGCAGGCATTAAAAACCGTTGACTGATAATATGCAAATGTATTATGCAAATAATTTCTGAATGGTCATTCAGGTGATTTAGAATCAATTCTTTCTTTTGTGAAACTGTAAATCCAATTGAGCTTTTAAACGTTGGACTCATCTGACATTGACAAACAGCTACATGACACATCACAAGAAAGGCAATTGTCAGAAACGCTTTAATGAAGTGAGGCGTCTGATGTTTGGATTTCTGATTTGCAGGAGTTTGTGATGATTGTTGTGTTTGGTCTGGAGTACATCATCCGCATCTGGTCTGCTGGATGCTGCTGCCGGTACAGGGGATGGCAAGGA[C/T]GACTGCGCTTCGCTAGAAAACCATTCTGTGTGATAGGTAAGATAAAAATATGTGTTTGTAGAGAGAGATGGATGTGCTGTGCTGGTTTTTGTGTTAACTGAACTGAATGGGAATCAATGACTGACTCAAACATTCTTAACCAACGAAAGATTTCTCTCTTAATTCCCTCTTCAGCAAAAACATGCAATAATGTACTAGTGAAAGATTACAGGCAATAAGTAACCAGTGCTATTTATATTTATTACACATATGGGGTATGTGGTATTGTGTTGTATGAGGGTAATTTAGGCTGAATGTATCAGTATATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAAGCACTGAACCTCATCTTTATTCATTAAGAGTGCAAGTCCCATCAGAACCCCATCAGCGCTGTAACTAACTCTGAATTATGAAACACAGAAG
Associated Phenotype:
Not determined