ZMP
kif6
Ensembl ID:
ZFIN IDs:
Description:
kinesin-like protein KIF6 [Source:RefSeq peptide;Acc:NP_001070899]
Human Orthologue:
KIF6
Human Description:
kinesin family member 6 [Source:HGNC Symbol;Acc:21202]
Mouse Orthologue:
Kif6
Mouse Description:
kinesin family member 6 Gene [Source:MGI Symbol;Acc:MGI:1098238]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36523 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36522 | Essential Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43002 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36523
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103662 | Nonsense | 136 | 693 | 5 | 20 |
| ENSDART00000103663 | Nonsense | 136 | 667 | 5 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 48954785)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 48716583 |
| GRCz11 | 17 | 48799212 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGACTGTTCATATTTATATATTTTTTTGCAGAACAACACAATGATTTA[T/G]ACAACCCACATATCTTACCTGGAAATCTACAATGAGTCTGGCTATGATCT
Long Flanking Sequence:
TACAGGAAAAAGCAGCAATCCGTGGCAAATCATACAACACAAATACTCAATTTCCTGAAAAACTGTCCAGCTGTCATTAATATCAGAAGCATTTTTTTCATACTTTATTACAGCATTGTTAATGTTGCATCTTTTAATAGTGTGCTGGCAGGTTATAATGGCACCATATTCGCCTATGGCCAGACAGGAAGTGGGAAGACCTTTACAATCACTGGAGGAGCAGAGCATTACAATGACAGAGGGATCATCCCCAGAACTCTTTCTTACCTATATCGCTATTTCAGTATGGTTAGTAGACAATTTCATAATATTTTTCTTGAAGGCATGCATTCTTTAAGCTTCTGATTTGAGTGCTAATTTTGACTGGAACCAATATTTGCTGCTGAAGTTTGGCAAAGGCTGCTGCTTTTATTTAGTAGTAATATTTCCGATTCAGCACTTCAATAGTAATCAGACTGTTCATATTTATATATTTTTTTGCAGAACAACACAATGATTTA[T/G]ACAACCCACATATCTTACCTGGAAATCTACAATGAGTCTGGCTATGATCTACTGAATCCCCAACATGAGGCATCTCGTCTAGAGGATTTACCGTCAGTCTCAATTTTGACCCTCCTTTATTTATGCTTTTCAGAACTGTTAATTATAATATCCTTTTTTTAAAAGATCTGATTAGGTGTGCAAGACTGAGACTAATTTGTTATAATTTAATATAATTTATTTCCAGTGTTCATTTTGACAGTAAATTTGAATTTAGTTTGAGTTTTTTTAGTCTCACTTTTTAAAAACTTTAGTCTTTAATCTTTAATCTATTTAATTTTAGTAATACAGCAATTTAGTCATTTTAGTTTAAAAGTGTATACCTCAGCCCACCGGAGATTTACTCGTCTGACAAACGATTCCTGCCTAAACTTTTTTGCCTTATCTTTTTTTGTTAAAAAAATCAGTAGATAGATACTATATTACTATTTGTCATAGTTTTATAAAGCTGAACTGAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36522
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:
Essential Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103662 | Nonsense | 392 | 693 | 11 | 20 |
| ENSDART00000103663 | Essential Splice Site | 328 | 667 | None | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 48933241)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 48695039 |
| GRCz11 | 17 | 48777668 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTTGTTTTGTAGAAGGACACAGGAGTATTATTCCTGTTTTTTAGGT[T/A]GGAAGGATTGGTGAATGTATATTTGGAGGACCCTGACTGTGAAGTAACAT
Long Flanking Sequence:
CATGTATTCTACATTATTTTTTAAATAAATAAATCCTCTTGCCTGCTTATGATATCTTTGTTGTTTGTTGTTTTTTTTCTGGCAGCTGATTGTCCATTTAAAAAAGGAGAATCAGTCTTTGAAGGAGCAGCTGGCTCTGATGACTGGAGAGCAAAGAAGTGACAAGTTAACCCAAGAAGAGATCCAGCAGTATGAACCTGTATTTCTTAACTTTGCCTGATTATTTTTTTGCTTATTTTGTTTTTACTTGGTGGCGGCATGGTGTGTCAGAGGTTATAACTGTTGCCTCACAGCAAGAAGGTTGCTAGTTCGAGTCCCGGCTGGGCCAGTTAGCATTTCTGTGTGTAGTTTGCATGTTCTCACCGTGTTTGCGTGAGTTTACCATACTCCCACATGTCAGTAATGGAACCTAAGCTGTCTAATTCTGCAGTTTATTTTGCTCTATGTGTTAATGTTTGTTTTGTAGAAGGACACAGGAGTATTATTCCTGTTTTTTAGGT[T/A]GGAAGGATTGGTGAATGTATATTTGGAGGACCCTGACTGTGAAGTAACATTAGACCTGGGGCCTGATATGAGGAAAATCCAGTTTTGTTTCTCTTTGCTAAAGGTGAGTGAATTAATTCATCGATTTATTGATTCCATTCAATTCCATCGATCTTTATTTCTATTGCATGTTTTACATTGTAGATTGTGTCAAAGCAGCTTAACATAGAGGAAGTTCTAGTAAATTAAAACTTCGTCAGTTCTGTTATTGCAGTTTAGTGTAATGTAAGCGTCACTGTTAAATGCCAACTATTGAAGAGCAACTCCAACAATGCACAGCTCCACTAGTCCCAAACCATTGGGACATTGATAGGATCTGTTGCTGTCAAGATTAGGCTGTTTTCTTAATAATTTCTTTTAAAAATATTGAATATATTTATTCAAAACACTCACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43002
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 > T
Consequence:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000103662 | Missense | 392 | 693 | 11 | 20 |
| ENSDART00000103663 | Essential Splice Site | 328 | 667 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 48933240)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 48695038 |
| GRCz11 | 17 | 48777667 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTTGTTTTGTAGAAGGACACAGGAGTATTATTCCTGTTTTTTAGGTT[G/T]GAAGGATTGGTGAATGTATATTTGGAGGACCCTGACTGTGAAGTAACATT
Long Flanking Sequence:
ATGTATTCTACATTATTTTTTAAATAAATAAATCCTCTTGCCTGCTTATGATATCTTTGTTGTTTGTTGTTTTTTTTCTGGCAGCTGATTGTCCATTTAAAAAAGGAGAATCAGTCTTTGAAGGAGCAGCTGGCTCTGATGACTGGAGAGCAAAGAAGTGACAAGTTAACCCAAGAAGAGATCCAGCAGTATGAACCTGTATTTCTTAACTTTGCCTGATTATTTTTTTGCTTATTTTGTTTTTACTTGGTGGCGGCATGGTGTGTCAGAGGTTATAACTGTTGCCTCACAGCAAGAAGGTTGCTAGTTCGAGTCCCGGCTGGGCCAGTTAGCATTTCTGTGTGTAGTTTGCATGTTCTCACCGTGTTTGCGTGAGTTTACCATACTCCCACATGTCAGTAATGGAACCTAAGCTGTCTAATTCTGCAGTTTATTTTGCTCTATGTGTTAATGTTTGTTTTGTAGAAGGACACAGGAGTATTATTCCTGTTTTTTAGGTT[G/T]GAAGGATTGGTGAATGTATATTTGGAGGACCCTGACTGTGAAGTAACATTAGACCTGGGGCCTGATATGAGGAAAATCCAGTTTTGTTTCTCTTTGCTAAAGGTGAGTGAATTAATTCATCGATTTATTGATTCCATTCAATTCCATCGATCTTTATTTCTATTGCATGTTTTACATTGTAGATTGTGTCAAAGCAGCTTAACATAGAGGAAGTTCTAGTAAATTAAAACTTCGTCAGTTCTGTTATTGCAGTTTAGTGTAATGTAAGCGTCACTGTTAAATGCCAACTATTGAAGAGCAACTCCAACAATGCACAGCTCCACTAGTCCCAAACCATTGGGACATTGATAGGATCTGTTGCTGTCAAGATTAGGCTGTTTTCTTAATAATTTCTTTTAAAAATATTGAATATATTTATTCAAAACACTCACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined