ZMP
zgc:171453
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC565014 [Source:RefSeq peptide;Acc:NP_001104651]
Human Orthologue:
KCNAB2
Human Description:
potassium voltage-gated channel, shaker-related subfamily, beta member 2 [Source:HGNC Symbol;Acc:622
Mouse Orthologue:
Kcnab2
Mouse Description:
potassium voltage-gated channel, shaker-related subfamily, beta member 2 Gene [Source:MGI Symbol;Acc
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24307 | Nonsense | Available for shipment | Available now |
| sa37682 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24307
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 |
|---|---|---|---|---|---|
| ENSDART00000086117 | Nonsense | 178 | 289 | 8 | 15 |
| ENSDART00000125074 | Nonsense | 221 | 440 | 9 | 15 |
| ENSDART00000132066 | Nonsense | 178 | 412 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 23 (position 21394337)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 21173644 |
| GRCz11 | 23 | 21100195 |
KASP Assay ID:
2261-7611.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACTGCATTTTTTTGACCTACAGGTCTAAGGGCATCACTGGAGAGACTT[C/T]AGTTAGAATATGTGGATGTAGTGTTTGCTAACAGACCTGACCCCAACACG
Long Flanking Sequence:
TCCAAGTATGATCCATAGTAGTTCCATCATATGGCTACAGGACTTGACAGATTTGTTGCTCACGTATTGGGGCTAGATACCACAGGGAACCTGCAAGGGTCTAGTAGAGTTCATTACCCTATTCTGCATTACAAAGGCAAAGTAACTACACACTTAGGCAAAATTGAGTTAAAATAGAATTTTGTGACATCTGTTCTGTCTGCTGCTTGAATTTTGACCCATTAAAAAAAGAGTGTCAAAATTGCTGCAACTACAAAATCCAAGCTGGCGTTAAAGTATTTTTACAGTCATGCTGCGCTTTTCCTTTGTAGGGTAGAGTGGTTTGGCACTGGTCATAATGCTTTGGCTTATCGGTGTAAATAAACTGTACTAAAGACTCCTAATATAAAGTGATTAAACAAAGCCCAAATAAGAACCTTTAAATTCTTTTGTCTTTAACAGCCATAAACATTACTGCATTTTTTTGACCTACAGGTCTAAGGGCATCACTGGAGAGACTT[C/T]AGTTAGAATATGTGGATGTAGTGTTTGCTAACAGACCTGACCCCAACACGCCAATGGAAGGTAAGTGTGCTTGATGAGATGCTGGCCAGTTTGTGTCATCTTTGTGTACCAGCACTGGAATGGCTCTCCTGATTGCTTTGCACTGAAGCATGGGATTAAAACAGACCAGCCACGCAGCTCTTAACTTATCAGGAATCAGACACTTTGAGACCAACAGCAGAGATTTGTTTAACCCCAAAACACAGCATTCCTAAAAATAGACAATCATCCCATTAAATTTCAATGCGTTACAACAGGGGTTTTCAAAGTGTGAGGCGCGCCTCCCCTGGGGGGCGCCAGAGCATGTCAGGGGAGGCGCGGGAAAAAATATAATATAATAAAAATATAATAATAAAGTTTAATTGTATGTATTTTTTTTTATTATATTTAAACGTTTATTATATGCCTGCTAATACAATGGGTCGGTTTTTGAGACCCACCCCGATTCAAAGCTGTAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37682
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 |
|---|---|---|---|---|---|
| ENSDART00000086117 | Nonsense | 204 | 289 | 9 | 15 |
| ENSDART00000125074 | None | None | 440 | None | 15 |
| ENSDART00000132066 | Nonsense | 204 | 412 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 23 (position 21397627)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 21176934 |
| GRCz11 | 23 | 21103485 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACAGTCTTTTGTTTGTTTGTTTATCACCAGGAGATCCATTTAACACTT[C/A]AAAATCAAGAACATTCATCATAGAAGGTACATGGTACCCTCAGTGAGAGT
Long Flanking Sequence:
TTATATCAAAGGCAGTATCTAAAAAGCATATTTGGCGCACTTTAAACTACTCTCTAAAATGATGATTTAAACACCTTCACAACTCAAATACTGATGAGATGTAAGATAACTTCACATTTCTGCCTAAAAATCCTCCAAAAAATGTCCTCATTGCCTTCTTCGCTGTAATTTCAATTACAAACACTGTTAACTGAGCTTAACTTGTCAAACCTGTGACAATGCCGTGCTGTACAGCTGTGAGGGCTTTGTGTACAGAGTGATGAGTGGCAGAGACTGATGCTTCTGAGGTCATGGCCATGTAGACATGATTGCTTGTGCACACACCACGTGACTTCATGAGTGGTCCTATTACTCCGGGACTTGCAGAATCTGCTCTGGTCCAGTTCTGCTGCCTTTTTTTTCCTCTCCCTTCAGAGATTTCATTCCATTTGCTGGTTGGTAAACCTCTTTTCACAGTCTTTTGTTTGTTTGTTTATCACCAGGAGATCCATTTAACACTT[C/A]AAAATCAAGAACATTCATCATAGAAGGTACATGGTACCCTCAGTGAGAGTTTTGACCTCCTGTCTCCAAAAGCATTTTATGGCTTTGATTTGTGATAGTCTGCCCTCTTTTTCCTGGTGTGAGAAACCTGACCATGTCCATAAAATGCTGAAGATTTCTAGACATTTCTATTTTAGGCCTGGTATGCCGTAGGACTGTCGAATTATTTGACTCTCCTGTCAATCTTGCAAGTTAAATTTAAAGAAGGTCATTGCATCTTACTGACCCATTTTCTTTGGTTTTCTTTCTTTTTTGTTGGATATTTACCATGCATCTTCATTCCATTTTAAAATATTATTCATTATTTACAGTAGTTTCCTTAGAAAAGCACTTGTCATGTAGGTTCTGTGTGGATTGTTTTGGGCTTTGCTTACTTTTGTTAAATCAGTTTGGACATAAGTAAAGCTGCAGATGTTATACTGTACACAAGTAAAGAATTAAAACACAGCGTCTGATCATAC
Associated Phenotype:
Not determined