ZMP
kif3b
Ensembl ID:
ZFIN IDs:
Description:
kinesin-like protein KIF3B [Source:RefSeq peptide;Acc:NP_001093615]
Human Orthologue:
KIF3B
Human Description:
kinesin family member 3B [Source:HGNC Symbol;Acc:6320]
Mouse Orthologue:
Kif3b
Mouse Description:
kinesin family member 3B Gene [Source:MGI Symbol;Acc:MGI:107688]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6722 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa39397 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa5805 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa6722
Status:
Confirmed mutation in F2 line
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 |
|---|---|---|---|---|---|
| ENSDART00000102519 | Nonsense | 238 | 775 | 2 | 9 |
| ENSDART00000122633 | Nonsense | 238 | 775 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 7789232)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 7781695 |
| GRCz11 | 23 | 7715667 |
KASP Assay ID:
554-4517.1 (used for ordering genotyping assays)
KASP Sequence:
TCATCAMCATTGAGTGCAGTGAGTTGGGTCCTGAYGGAGAGAACCATATT[C/T]GAGTTGGRAAGCTTAACCTTGTTGACCTGGCAGGAAGTGAAAGACAGACC
Long Flanking Sequence:
TGGAGCTCTACGACGAGACTTTCCGCCCGTTAGTGGACTCTGTACTGTTTGGCTTCAATGGGACCATCTTTGCATATGGCCAGACTGGCACTGGAAAGACTTACACAATGGAAGGGGTACGAAACGACCCGGAAAGAAGGGGTGTGATCCCAAACTCATTTGAACACATTTTCACACACATCTCCCGCTCTCAGAACCAGCAGTACTTGGTCAGGGCTTCATATTTGGAGATTTATCAGGAGGAGATCAGAGACCTTTTGTCAAAGGACCAAGCACGTCGTTTGGAACTCAAAGAGCGACCAGACACAGGTGTCTATGTTAAAGACCTGTCTTCGTTTGTCACTAAAAGTGTTCGTGAGATTGAGCATGTGATGAATGTGGGGAACCAGAACCGCTCAGTTGGTGCAACAAACATGAATGAACACAGTTCTCGCTCTCATGCCATCTTCGTCATCACCATTGAGTGCAGTGAGTTGGGTCCTGACGGAGAGAACCATATT[C/T]GAGTTGGGAAGCTTAACCTTGTTGACCTGGCAGGAAGTGAAAGACAGACCAAAACCGGTGCTCAAGGTGAACGCTTAAAAGAAGCCACTAAAATCAATCTCTCCTTGTCAGCTTTGGGAAACGTCATCTCAGCGTTGGTGGATGGAAGAAGCACCCATATCCCGTACCGTGACTCTAAGCTTACAAGACTTCTTCAAGACTCCTTGGGTGGAAACGCCCGAACGGTTATGGTGGCCAACATTGGACCAGCTTCCTACAATGTAGAGGAGACTCTAACGACGCTACGCTATGCAAACCGCGCCAAAAACATCAAGAACAAACCCCGTGTCAATGAAGACCCCAAGGATGCCCTTCTTCGGGAGTTTCAGGAGGAGATTGCCCGCTTGAAAGAACAGTTGGAGAAAAGGTCTGGAAGGAAGAGGAGGAGAAGGAGGAGAAGAAGGGTTGGAGAAGGAGGAGAGGAGTTTGAGGATGGGGAGGATGAAGAGGATGATGATGAT
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
trunk ZFA:0001115 |
bent PATO:0000617 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa39397
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 |
|---|---|---|---|---|---|
| ENSDART00000102519 | Nonsense | 427 | 775 | 2 | 9 |
| ENSDART00000122633 | Nonsense | 427 | 775 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 7789799)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 7782262 |
| GRCz11 | 23 | 7716234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGGAGTGGATGCAGATAAGAACATTGCAGATTATTGGCATGAGCAA[C/T]AGGAGAAGCTGGAGAAGGAGAGGAGAGCCATCATGGAGGACCACAGTCTG
Long Flanking Sequence:
GTGAACGCTTAAAAGAAGCCACTAAAATCAATCTCTCCTTGTCAGCTTTGGGAAACGTCATCTCAGCGTTGGTGGATGGAAGAAGCACCCATATCCCGTACCGTGACTCTAAGCTTACAAGACTTCTTCAAGACTCCTTGGGTGGAAACGCCCGAACGGTTATGGTGGCCAACATTGGACCAGCTTCCTACAATGTAGAGGAGACTCTAACGACGCTACGCTATGCAAACCGCGCCAAAAACATCAAGAACAAACCCCGTGTCAATGAAGACCCCAAGGATGCCCTTCTTCGGGAGTTTCAGGAGGAGATTGCCCGCTTGAAAGAACAGTTGGAGAAAAGGTCTGGAAGGAAGAGGAGGAGAAGGAGGAGAAGAAGGGTTGGAGAAGGAGGAGAGGAGTTTGAGGATGGGGAGGATGAAGAGGATGATGATGATGATGATGAAGACGAAGAGGAAGGAGTGGATGCAGATAAGAACATTGCAGATTATTGGCATGAGCAA[C/T]AGGAGAAGCTGGAGAAGGAGAGGAGAGCCATCATGGAGGACCACAGTCTGGTGGCAGAGGAGAAACAGCGGCTGCTGAAGGAGAAGGAGAGGAAGATGACTGACCTGCACAAAGAGAAAGAGGCATCAGAGATGCTGACAGCCAAAGTTAAGGTTAGAAACTTCAAGCTTTGAATGAAATACAAATACATAATGGAGTCTGTAAGGTGTTAAGAAAAATTTCTGGATTTACAATAGGGATGTCCCAATTAGATTTTTTTTTAATTTTGAGAATCTATCGATACCGAAACCCAATCTGATACTTCTATAATACATAAAAAGAATAAAGAAGAGCAAAGAAACAGATTCAGGATGTACATTCAACAACTCTGTTTACAAACAGAGCACTTCTGTGAGGTAGCTTAAACAATCAAGTGATAAATGATATAAATTCTTCACTTTTGGAATTTAGTGCAACAGTAAATATAAAACCAAACAGCACCTCAACTTAAGATACCCGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5805
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000102519 | Essential Splice Site | 631 | 775 | 7 | 9 |
| ENSDART00000122633 | Essential Splice Site | 631 | 775 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 7798783)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 7791246 |
| GRCz11 | 23 | 7725218 |
KASP Assay ID:
554-3518.1 (used for ordering genotyping assays)
KASP Sequence:
AGCATCCTTCCTGTTTTCATTTTAATGCTTCTTTCTCTGTATTATTTTCA[G/A]CAGTGATCATCAGATGATGAAAAGGCCTGTTTCYGCAGTGGGCTACAGAC
Long Flanking Sequence:
GACGGTGTGAACACGTGACAAGGGGGAGACAAGTGAACTTGGGTTTGGACCAGGAAATCAACCCAAGTGTGACAGCACTTCTAGGCTTTTTTGTTTTGTTTTCTAAGAATTTACCTCATTTCCTAACTAAAGTCTTAGTTTTAATACTCCAATTCGAACAATATATACTTAAATAGATTTTAATCATGGAATAGTGATCTAACTTTAAAGTAAATTGACATAAAAATGAAAAACAAACATTGCCACTACTGACATGAAAACATTTGCATTGTATCTACCAGACACTTAATCATAGAGAACTTCATCCCAATGGAGGAGAAGAACAAGATTGTAACAAGAGCCACATTTGATGAAGAAGACGATCTCTGGAAAATGACCCCCATCACCCGTATACAAAAGTATGTCGGCTTATTTTAGAAATGTAAAACTTATTTACAAACTGAGGCCATCAGCATCCTTCCTGTTTTCATTTTAATGCTTCTTTCTCTGTATTATTTTCA[G/A]CAGTGATCATCAGATGATGAAAAGGCCTGTTTCTGCAGTGGGCTACAGACGGCCTCTGAGTCAGCATGCCCGTATGGCCATGTTGATGCGGCCTGATGTCAGATACAAGGTATGCTGACACTGTTGCCATAATCCTCCACATGGCACAACACAAAGGCTTCAGTAACAATACACCCCCACTCTTCACAGCGACACAGATGAGCTTAGGAGAATCAAATGCATGACATGTCCTTGCTTATTCACTTTTGTTTATTTTAGTGAGGTTTTATTGATTTTCTGAAAGGTAATATGATATTGTTATATACAATAATGGAATAAGCCGAATGAAGTCAGGGTTTACAGAAAATTTATAACAGCTAATTGGTGTTTGTGCCTTAACACACTTGTTTTCACTGTATTGCATTAATACACTGTTTTGCATTTATTAAACACTTTTATAACTATAAATAGTTTATTTGGCCCAGTACCAGTATGGGAATGGTTGCTGATTAACTGTCACA
Associated Phenotype:
Not determined