ZMP
si:dkey-210m15.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate kinesin family member 16B (KIF16B) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
KIF16B
Human Description:
kinesin family member 16B [Source:HGNC Symbol;Acc:15869]
Mouse Orthologue:
Kif16b
Mouse Description:
kinesin family member 16B Gene [Source:MGI Symbol;Acc:MGI:1098240]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19595 | Essential Splice Site | Available for shipment | Available now |
| sa25671 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19594 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19595
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109333 | Essential Splice Site | 90 | 1318 | 4 | 30 |
| ENSDART00000131674 | None | None | 152 | None | 4 |
| ENSDART00000140079 | None | None | 491 | None | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 51776244)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 50622511 |
| GRCz11 | 1 | 51266310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTTCGCGAGCTGAATATTGGCTCTGAGTCATGACTTGCTACTTTATA[G/T]GGAGACCTCGGACTGATCCCACGCATCTGTGAAGGATTATTCAGCCGGAT
Long Flanking Sequence:
AACAATAAAACTTTTAAATGGCCCCATTTATACCGAATACTAATCAGGTCTGATTCGTAATTAATCCTCTGAGCGTTTGTGTTCAGAAAGGTTTGTTTCTTGATATGTAACAACCATCTGGTACATTTAAAAACAAAAATAGTGAGATTCAGGGCTGGCTTCCCAGAGGCAGATTTTAAATCCTGATCCTAAAGGCATTGTTAGCAGTACATTTGAGTCCATATCTTGACTTTATGATTAGCTTTTGATTTTTTTTTTTGCACTGACACATTAACCCATGCAGTAACATCCCCCGCATGTATGTGTGATTTCAGGTGTTTAAGGATCTGGGCACAGATGTGTTGAAGTCAGCATTTGAAGGATATAATGCTTGCATCTTTGCTTATGGTCAGACTGGATCAGGGAAGTCACACACCATGATGGGAATCCCTGTAAGTTCTTTCTGTTTAAACTTTTCGCGAGCTGAATATTGGCTCTGAGTCATGACTTGCTACTTTATA[G/T]GGAGACCTCGGACTGATCCCACGCATCTGTGAAGGATTATTCAGCCGGATTTCAGGAATGACTCGGAGAGATGAAGCCTCTTTCCGTACGGAGGTCAGGTAAGTTGAGTTCTGGAGTCATTGATGAACAAAAACATGAGCAGAAACAGATAACTCATAGTGTGCACCATCGATCTGCATTATTAGCTTTAGCAATAAGAAAAAAATCTAGGGATCACCGATGTTGAATTTCTGACCAATAACTAGGCCCACACACAATCTGCGCACACAGAAATCCGCAGATTTCCAGCCCATCATTAAGTCTATTTCTTTTCTTGTGTAAATGTGTGTACATTTATTTTTATTCAATCAATTTTCAATCAATCAAATCAATCAATCAATCAAATTTACAATGCAGTTTGTAATAAAATATTTCTGTCTTTTAGTAGATATATTATATGAGAAACTTGCTTTGTTTACCAAAAAAGTGGATTTAATTGGATTTTCATTGTTATTATATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25671
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109333 | Nonsense | 143 | 1318 | 5 | 30 |
| ENSDART00000131674 | None | None | 152 | None | 4 |
| ENSDART00000140079 | None | None | 491 | None | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 51774892)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 50621159 |
| GRCz11 | 1 | 51264958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAACGAGCGCGTGCGGGATTTGTTACGGAGAAAGATGGCAAAAACTTA[T/A]AACCTCAGAGTCAGAGAGCACCCTAAAGAGGGACCCTATGTAGAAGGTAA
Long Flanking Sequence:
ATTAACGAAAATCAAAATACCAGTAAAATAATAAAAATGTGGCAGGTAGCAAGCCTGTGAAGAGGTTCAACCTGCAGAAAAATACATAATTTATTGGCTTTGAGATACCGGTTGAATTTTTTTTATTGGACCGATATTGATAAACATTATATCGGCCGATATGGCTGCCGATATAGCATACATCTCTACTGATTTCAGTCAGTTTTCTGCCATAAACTCAGACATTTAAGGGTTATTGACTATTTATTTATTTAGGTATTTAATATTTATTGCCAATGTTACTATATCTGCCTTATAGAAACCGATAGCACAGAAATGATGCTCTTGCAGTAGCTATAGTAATGTGCGTGTACAAAATAAAAGTCATTTGAAGTGTGCATGTGGAAATACAGCTCTTACTGTGATTTATTTATTTATTTTTTTGTTTATGCTGGCAGCTATTTGGAGATTTACAACGAGCGCGTGCGGGATTTGTTACGGAGAAAGATGGCAAAAACTTA[T/A]AACCTCAGAGTCAGAGAGCACCCTAAAGAGGGACCCTATGTAGAAGGTAAGACCGTGACTTTAAACCGCAACCAAAAATCTCCAAATTTATGTAATGGATAACAGACATTTAATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTATATATATATTTATATATATATATATATATATATATATTTTTTATATATTTATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTACCTTAATAAAGATGTTATGTCTTCTAGTATTAACTAAGCAAATATACCTCTTGACTTTCATAGTACATAACAGTTTTTAACGATATTGTTAAATGTATTTAGCTATTAGGCAGATTTTAAAATTGCAATATCAGAAAATATTGAGTAAATATCAGTAAAAATTAGCAATACTTTACATAACTATGGAACAACTTACGATATTTTAATAAATATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19594
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 |
|---|---|---|---|---|---|
| ENSDART00000109333 | Nonsense | 557 | 1318 | 16 | 30 |
| ENSDART00000131674 | None | None | 152 | None | 4 |
| ENSDART00000140079 | Nonsense | 192 | 491 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 51765846)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 50612343 |
| GRCz11 | 1 | 51256142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTCTCACCAGCCTGAGCTTATCCATGTCTGATCTGTCTAAATCCTGT[G/T]AAAACCTCTCCACCGTCATGCTCTATAACCCTGGGTAAGCCGCTGTGTGT
Long Flanking Sequence:
ACATTTCAGACCATCATGAACGTTCTGTTTGCAGAGGCTGGATTGAAATAATGTTCCATTTCTATCACAGAACAATTGATCATTTTCATAAGACCTCAATTTATACCATTACCATATATGGTTCTTTTCCTGATTAAGGGTTAAATAGTTCACCCAAAAGTAGAAATTCTGTCATCATTTACTCCCTTTAAATGATTAAAATCGATTTTCTGTATTGTTCTATTGAACACAAAAGAAGATATTTTGAAGAGAGCTGCAAACCTGTGAGCATCCACTTCCATAGTATTTGTTTTTTTCTACTATGGAAGTCAGTGGTAACAGATTTTGTTCAGCATTCTTCAAAACAGCTTCATTTGTGTTGAACAGAAAAAAAAAAAGAATTAGAGAGTAAATCTTCGTATTTGAGTGAACTGTCCCTTCAATGTCTGCTCTGTGTTTCTCCTCAGAGTGGCCTTCTCACCAGCCTGAGCTTATCCATGTCTGATCTGTCTAAATCCTGT[G/T]AAAACCTCTCCACCGTCATGCTCTATAACCCTGGGTAAGCCGCTGTGTGTGTGTATGACCGAGCGAGTGGCATCTACTTCCTCAGTTCCTCCCTCTCTTCCTCCCAGGAGCCTCCTCTTCCCTCCTCTCTCCATCCTCCTCGCTCTTCATGCTCTCCGGCAGCATCGCTGGTACTGCTAATGCAAAGTGCATTAAAACAGCTCGCAGGGAATGCTAATGGCTCGTTTTCACTGAGCAGTACAGTACAGGTCTATTTCCATTTCTACTCTCAGAAGTATTAAAATAGCAAACGGTACTGTACAAGCCTGTTATACTTCAAATGAAATAAAATAGAACTGACAAAACAATGTTCAATTTGGGAGTTCGAAATGGCTCACCAAACCAATTGAGTTAAATTAGGCTGTCCAGTCTCTGTGCTCTGTCCATTATTTCCACTGTATCCGTTCACCTGAGGGAACAGAGGGTATCCACAGGGTTTGAAAAAGTCTTAATGTCTTAAA
Associated Phenotype:
Not determined