ZMP
kcnip1b
Ensembl ID:
ZFIN ID:
Description:
Kv channel interacting protein 1 b [Source:RefSeq peptide;Acc:NP_001008632]
Human Orthologue:
KCNIP1
Human Description:
Kv channel interacting protein 1 [Source:HGNC Symbol;Acc:15521]
Mouse Orthologue:
Kcnip1
Mouse Description:
Kv channel-interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1917607]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21722 | Essential Splice Site | Available for shipment | Available now |
| sa12212 | Essential Splice Site | Available for shipment | Available now |
| sa27600 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa15042 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21722
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000035188 | Essential Splice Site | 62 | 215 | 3 | 8 |
| ENSDART00000109420 | Essential Splice Site | 62 | 215 | 3 | 8 |
| ENSDART00000035188 | Essential Splice Site | 62 | 215 | 3 | 8 |
| ENSDART00000109420 | Essential Splice Site | 62 | 215 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 22226069)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22056407 |
| GRCz11 | 10 | 22025859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAAAAATGAGTCTCGTAGCAATATTATGACCTGTTTGTTTTCCCCCAC[A/T]GGAGTGTCCAAGTGGAGTGGTGAATGAGGACACTTTTAAACACATTTATG
Long Flanking Sequence:
TTAGATGTTACAGTACATAACAATATGTTTACTGCTTTTTTTCATTTTTTTATTTATTTTATACTAGTATTTTATTTACATTATCACATTTCTATTTATAAATGTAATTTTTTTTAGCATGAAAATACTAAAAAGTGGCATGTTTTCAGGCATGTTTATGTTATTTTTTAACACAATACAAATGTTTTAAATTTAGAAGGGTTAAGAAACTCTTGGTTGAATAAAACATTTTGTATTCTGTCATTTTCTTAAAAGAATTATCAAATAATAATAAATCAAATAATAAAATGAAAACAAATAATTATAACAATAATTGTGGTTGAAATTTTGACACCAGTAAAATAAATATAACAAATTCAGTCAAACACCTAAAAAAATCAATCCAAAACTATATTTATCAAGTGGTCTCCTAAATTGTTTCACATATTTCTATACTACTGGTTTGAAATATCCAAAAATGAGTCTCGTAGCAATATTATGACCTGTTTGTTTTCCCCCAC[A/T]GGAGTGTCCAAGTGGAGTGGTGAATGAGGACACTTTTAAACACATTTATGCACAATTTTTTCCACATGGAGGTACTTTCCAAACAATTCTTTAGTTAACACCAAAAAGAACACCTGTCATCACTTTGAGACCCTCATGTTTCTCCATTCCTATAAGAAATTTCTTCATCTTCAGTAGACAAATAAAAATATTTCAATCAAATCTGAAAGATTTCTGTCTCTCCCTTCAATGTGTTTTCAAAATATTTATAAAGATATTTTAAAAAATCCATATGAACTTCATGAGTTCACTCATGGACTCTCCTTCAGCATAGTCATTGATGTTACAGGGTTTGCCACAGCGGAATGAACCACCAATTACTCTGGAATTTGTTTTATGCAATGGATTAAAACATACAAAATATTCATTTGTGTTTAAGTTTATAAATTAACATGCACTGTAAAAAATTCTAGGTTCCACACAATGATTTGTGTTGGGACAACATGAAGGAATCAAGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12212
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000035188 | Essential Splice Site | 62 | 215 | 3 | 8 |
| ENSDART00000109420 | Essential Splice Site | 62 | 215 | 3 | 8 |
| ENSDART00000035188 | Essential Splice Site | 62 | 215 | 3 | 8 |
| ENSDART00000109420 | Essential Splice Site | 62 | 215 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 22226069)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22056407 |
| GRCz11 | 10 | 22025859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAAAAATGAGTCTCGTAGCAATATTATGACCTGTTTGTTTTCCCCCAC[A/C]GGAGTGTCCAAGTGGAGTGGTGAATGAGGACACTTTTAAACACWTTTATG
Long Flanking Sequence:
TTAGATGTTACAGTACATAACAATATGTTTACTGCTTTTTTTCATTTTTTTATTTATTTTATACTAGTATTTTATTTACATTATCACATTTCTATTTATAAATGTAATTTTTTTTAGCATGAAAATACTAAAAAGTGGCATGTTTTCAGGCATGTTTATGTTATTTTTTAACACAATACAAATGTTTTAAATTTAGAAGGGTTAAGAAACTCTTGGTTGAATAAAACATTTTGTATTCTGTCATTTTCTTAAAAGAATTATCAAATAATAATAAATCAAATAATAAAATGAAAACAAATAATTATAACAATAATTGTGGTTGAAATTTTGACACCAGTAAAATAAATATAACAAATTCAGTCAAACACCTAAAAAAATCAATCCAAAACTATATTTATCAAGTGGTCTCCTAAATTGTTTCACATATTTCTATACTACTGGTTTGAAATATCCAAAAATGAGTCTCGTAGCAATATTATGACCTGTTTGTTTTCCCCCAC[A/C]GGAGTGTCCAAGTGGAGTGGTGAATGAGGACACTTTTAAACACATTTATGCACAATTTTTTCCACATGGAGGTACTTTCCAAACAATTCTTTAGTTAACACCAAAAAGAACACCTGTCATCACTTTGAGACCCTCATGTTTCTCCATTCCTATAAGAAATTTCTTCATCTTCAGTAGACAAATAAAAATATTTCAATCAAATCTGAAAGATTTCTGTCTCTCCCTTCAATGTGTTTTCAAAATATTTATAAAGATATTTTAAAAAATCCATATGAACTTCATGAGTTCACTCATGGACTCTCCTTCAGCATAGTCATTGATGTTACAGGGTTTGCCACAGCGGAATGAACCACCAATTACTCTGGAATTTGTTTTATGCAATGGATTAAAACATACAAAATATTCATTTGTGTTTAAGTTTATAAATTAACATGCACTGTAAAAAATTCTAGGTTCCACACAATGATTTGTGTTGGGACAACATGAAGGAATCAAGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27600
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000035188 | Essential Splice Site | 179 | 215 | 6 | 8 |
| ENSDART00000109420 | Essential Splice Site | 179 | 215 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 22228685)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22059023 |
| GRCz11 | 10 | 22028475 |
KASP Assay ID:
2260-3186.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTTTAAAAGGAGACGTACCAAAGGCGCATGTGGATGCTTTCTTTGAG[G/A]TCAGTCATTAGTCTGTTAATTATTCAGTCATTCTTGGAGGTTACATTAAA
Long Flanking Sequence:
AATATTACATACGATTTCAGAGAATTAACATATTTAATGTTTTCATCTGTCGCCACTCCTTTAACAGATGCCAGCACATATGCACATTATCTCTTCCATGCGTTCGACACCAGAAATAATGGATCAATAAAATTTGAGGTATGAAGCCTAGATGAGAGCAGAATTAAAATAATGACATCGCACAGAGAAATGATTTTCTCACTCTCTCAGGACTTTGTGATGGGACTATCCACTCTATTGCGGGGGACAGTCAGAGATAAGCTGGAATGGACATTTCATCTCTATGACATCAACAAAGATGGATTCATCAATAAGGAGGTATGTCATATTTAAAGGGCAGGTGTAAATGTCATTACTTGATTCAGTAACGAATTCATTCTTCATGTACCTTTCAGGAAATGACAGAGATAGTGAGAGCGATCTACGACATGATGGGGAAATACACATATCCAGCTTTAAAAGGAGACGTACCAAAGGCGCATGTGGATGCTTTCTTTGAG[G/A]TCAGTCATTAGTCTGTTAATTATTCAGTCATTCTTGGAGGTTACATTAAAATTTAAAAACATTGGATTTTTTGTATGCTTTTTTGTGCTTTTGAAAACTGCTTTCACTCAATTTAGTTGATTATAACAATGTAATCGAAATTCTGAGAAATTTTTCATGTTCCTTCTGTTTAATCCCTTCATTATCAGCAGTCACCACGGCAGAATAAACTGCCATTAACATATTAAATTATTAACATTTTTTTTAATCTCTGGTCTTGAGTGCCACATATTTCAGAAATCATTCTATAGTAGTGGTGAAGTACTGCTTAGTTATATTAAACTATTGCTGATGGTTAATTATTAAAATAGTTTTTGCTATTTTTTAAGTATTAGTGTGAACTGTTTTTGTTGCTTTTTTTTGGCTAAATTTTGTGAATGATTTTTATAGCACGAGCTGTCACAGCAAGCTAAATACACTTTCACTCTTTCACAGAAAATGGACAAAAACAAAGATGGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15042
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000035188 | Nonsense | 187 | 215 | 7 | 8 |
| ENSDART00000109420 | Nonsense | 187 | 215 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 22229181)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22059519 |
| GRCz11 | 10 | 22028971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTAAATACAYTTTCACTCTTTCACAGAAAATGGACAAAAACAAAGAT[G/T]GAGTTGTAACATTGGAGGAGTTTGWCCTTGCCTGCCAAGAGGTACWTTCA
Long Flanking Sequence:
TGAGGTCAGTCATTAGTCTGTTAATTATTCAGTCATTCTTGGAGGTTACATTAAAATTTAAAAACATTGGATTTTTTGTATGCTTTTTTGTGCTTTTGAAAACTGCTTTCACTCAATTTAGTTGATTATAACAATGTAATCGAAATTCTGAGAAATTTTTCATGTTCCTTCTGTTTAATCCCTTCATTATCAGCAGTCACCACGGCAGAATAAACTGCCATTAACATATTAAATTATTAACATTTTTTTTAATCTCTGGTCTTGAGTGCCACATATTTCAGAAATCATTCTATAGTAGTGGTGAAGTACTGCTTAGTTATATTAAACTATTGCTGATGGTTAATTATTAAAATAGTTTTTGCTATTTTTTAAGTATTAGTGTGAACTGTTTTTGTTGCTTTTTTTTGGCTAAATTTTGTGAATGATTTTTATAGCACGAGCTGTCACAGCAAGCTAAATACACTTTCACTCTTTCACAGAAAATGGACAAAAACAAAGAT[G/T]GAGTTGTAACATTGGAGGAGTTTGTCCTTGCCTGCCAAGAGGTACATTCACATTATGTGCAATTTCATTAGTCTTTTGCTGGGGTGCCCAAACTCTGTCCTGAAGGGCTGTTGTCCGGCATAGTTTAGATCCAACCCCAATCAGACACACCTGGGATAGCTAATCAAGCTGCGGTCACACTGGACTTTTATTCCCATAGACTTCCATTCATATGCACGCAAATACGTCAGACTGGAAAGGCAAGCTCGTGCAAAAGGTTTCGCAGTTCGCTGCATTGCAAAGTTCAAGCTTGGTGAACTCTGACCTGCCAAATCACATCACTTGACTGCGTGACACCAACCATGGGGGTTAAAACATGACCTCTCTGGACAGAAATTTAAAATATGAACCAATCGCTTGCTTTTTAAATGTCTAATCATCTTGTTTAATCCCACCCCTTTTTACATCACCCTACAGAATTTCACACACACAAATTCTAGTGTGACCGCTGCTTTAATAGG
Associated Phenotype:
Not determined