ZMP
kif17
Ensembl ID:
ZFIN ID:
Description:
Homomeric kinesin Kif17 [Source:UniProtKB/TrEMBL;Acc:C0L098]
Human Orthologue:
KIF17
Human Description:
kinesin family member 17 [Source:HGNC Symbol;Acc:19167]
Mouse Orthologue:
Kif17
Mouse Description:
kinesin family member 17 Gene [Source:MGI Symbol;Acc:MGI:1098229]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18340 | Nonsense | Available for shipment | Available now |
sa27822 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9256 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12627 | Nonsense | Available for shipment | Available now |
sa256 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18340
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 |
---|---|---|---|---|---|
ENSDART00000129918 | Nonsense | 92 | 823 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 38819468)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37386487 |
GRCz11 | 11 | 37653692 |
KASP Assay ID:
2260-4599.1 (used for ordering genotyping assays)
KASP Sequence:
CGTTACAGGGTGTAACTGAGGGCTACAAKGGGACCATTTTTGCTTATGGA[C/T]AAACAGGCAGCGGCAARTCGTTTACAATGCAAGGTGTACCAGATCCTCCT
Long Flanking Sequence:
CCTAAACAATTCACGTTTGACGGGACTTATTATATAAACCACTCCACTGAAGAGGTCTACAACGAGATCGCGTATCCTCTGGTGGAGGTAATATTGATGTTTTTTTGTGTGTATGATTTAGCATGACTGTAAGAGTCTCTGTAGAGACACTTAACTTTCCAGTGTGTGTGTGTGTGAATGCCAATATGTGTGTTATCTGATACCTGTTGTCCTTTATCTGAAACTAAACACCATAGAGTTAAAATCAGTCACGGAAGTAACCTACAGCCCTTCTTATAATTGATTATTTACTAGATGTGCTTGTAAGCTGGGCCCTTAAGTCTCTATATATACAACACTGAGGACCTGAATATCTATCTATCCATCCATCCATCCGTCTGTCCGTCCGTCTATCTGTCTATCTCTGTCTGTCTGTCGTTCTTTCATCAGCCTTATATTCTCATTCTTTTGCGTTACAGGGTGTAACTGAGGGCTACAATGGGACCATTTTTGCTTATGGA[C/T]AAACAGGCAGCGGCAAGTCGTTTACAATGCAAGGTGTACCAGATCCTCCTTCCCAGAGAGGAATCATCCCTAGAGCTTTTGAGCACATCTTTGAGACAATCCAGGTAACCAGTTTACAAAACAAAACATTTTTTTTTCTAAGAGTTTATTTGCAAATTCAGATGACTAAATTACATATACAGTTGAAGTCAGAATTATTAGCCCCCTTTTAATTTTAATTTTCTTTTTAAAATATTTCCCAAATGATTTTTAACAGAGCAATGACATTTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGTAAGTCTTATTTGTTTTATTTGGGCTAGAACAAAAGCAGTTATTAATTTTTTTAAACACTATTTTAAGGTCAAAATTATTAGCCCTTTTAAGCTAATTTTTTTCGATAATCTACAAAACAAACCATCATTGTACAATAACTTGCCTAATTACCCTAACCTGTCTAGTTCACCTTATTAACCTAGTTAAGCCTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27822
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129918 | Splice Site, Nonsense | 126 | 823 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 38819570)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37386589 |
GRCz11 | 11 | 37653794 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGAGAGGAATCATCCCTAGAGCTTTTGAGCACATCTTTGAGACAATC[C/T]AGGTAACCAGTTTACAAAACAAAACATTTTTTTTTCTAAGAGTTTATTTG
Long Flanking Sequence:
TTTTGTGTGTATGATTTAGCATGACTGTAAGAGTCTCTGTAGAGACACTTAACTTTCCAGTGTGTGTGTGTGTGAATGCCAATATGTGTGTTATCTGATACCTGTTGTCCTTTATCTGAAACTAAACACCATAGAGTTAAAATCAGTCACGGAAGTAACCTACAGCCCTTCTTATAATTGATTATTTACTAGATGTGCTTGTAAGCTGGGCCCTTAAGTCTCTATATATACAACACTGAGGACCTGAATATCTATCTATCCATCCATCCATCCGTCTGTCCGTCCGTCTATCTGTCTATCTCTGTCTGTCTGTCGTTCTTTCATCAGCCTTATATTCTCATTCTTTTGCGTTACAGGGTGTAACTGAGGGCTACAATGGGACCATTTTTGCTTATGGACAAACAGGCAGCGGCAAGTCGTTTACAATGCAAGGTGTACCAGATCCTCCTTCCCAGAGAGGAATCATCCCTAGAGCTTTTGAGCACATCTTTGAGACAATC[C/T]AGGTAACCAGTTTACAAAACAAAACATTTTTTTTTCTAAGAGTTTATTTGCAAATTCAGATGACTAAATTACATATACAGTTGAAGTCAGAATTATTAGCCCCCTTTTAATTTTAATTTTCTTTTTAAAATATTTCCCAAATGATTTTTAACAGAGCAATGACATTTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGTAAGTCTTATTTGTTTTATTTGGGCTAGAACAAAAGCAGTTATTAATTTTTTTAAACACTATTTTAAGGTCAAAATTATTAGCCCTTTTAAGCTAATTTTTTTCGATAATCTACAAAACAAACCATCATTGTACAATAACTTGCCTAATTACCCTAACCTGTCTAGTTCACCTTATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGAATAGAAGTGTCTTGAAAAATATCTAGTAAAATATTATTTACTGTCATCATGGAAAAGATAAAATAAATCAGTTATTAGAAATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9256
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129918 | Nonsense | 439 | 823 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 38834527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37401546 |
GRCz11 | 11 | 37668751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCYGARCAAGAGTCTAAAGKCAAACTCCAGGAGGACATCGCTGCCTTG[A/T]GAACATCATATGAGACYAGGCTCTCTTCTTTAGAAAGGTCCAGAGGTAGT
Long Flanking Sequence:
CATATATTCTCTGACAAATGGATAAAATATTCATTTTCAAAATGGGGTGTACTCTGTTATGCTGAGCACTGTAATTCCCCTGGAAACTGATCAAATGTGTACCATCAATGCATTATAAAGTTCATACTAAGAATGTTATGATATGAGATGCTGATCAAAAGCAATAGACGTCAGTCAGCATCTTGTATTGGTTGCAGCTGTTTTTTGTGATTTGAGCAGGATGATTGGGCATTCAATTGTTTTTATGAATCTTCAGATGGAAAAAAACAGAATTTTGAAAATCTCTGCAGCACTATAATTCCTTTGTGCTGTTATCATTAAAAACACAAATAGATTATAGGTATCAAACTTGTAAATGTGCCTTAATTAAGCCAAATGCAGTGATGTGTAATGTGTGAATGTACATTTAGGAATATGAGAAGAAACTGGCGAGGCTGCAGGCAGAGTATGATGCCGAACAAGAGTCTAAAGTCAAACTCCAGGAGGACATCGCTGCCTTG[A/T]GAACATCATATGAGACCAGGCTCTCTTCTTTAGAAAGGTCCAGAGGTAGTCGAACACACACCACTGGTAATGTTGAAATTTGATGTCCTTAGGTCAGTCTTTTGGTTCTGTATGTTATTGATCTGTAGAATCTTGTCGTTCTCTTAAATCAGGTGGTGTTCATCTGCAACAACATAAAGAAGAGCCCATCACTGCATCTGCGGCTTCACAAGAACAGGCTAAGATTGACCACAGTGAATCTGAGGTGTTTTTATTTCGCATTAGTAAATGTATTTAACATTTTTAAAATGTTTTTCATCTGCATATTTAATGTTGTTTAATGACTTCACAAATATAAATGACCCTTTTGTTTAGGAGAGACCGTCTTCTGTTGATGCCACTGTCAAAGGAGCTGCCAGTGGAGAAAGTCAAATTTTAGATTCGGTTGTAGTTGACATACCAGGTCAGCTGGACCAGAAGCTTGCTTTGGAGAGGTGAGATGCTTAACTGGCCTTAAAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12627
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129918 | Nonsense | 442 | 823 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 38834538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37401557 |
GRCz11 | 11 | 37668762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTCTAAAGKCAAACTCCAGGAGGACATCGCTGCCTTGWGAACATCATA[T/A]GAGACYAGGCTCTCTTCTTTAGAAAGGTCCAGAGGTAGTCRAACACACAC
Long Flanking Sequence:
TGACAAATGGATAAAATATTCATTTTCAAAATGGGGTGTACTCTGTTATGCTGAGCACTGTAATTCCCCTGGAAACTGATCAAATGTGTACCATCAATGCATTATAAAGTTCATACTAAGAATGTTATGATATGAGATGCTGATCAAAAGCAATAGACGTCAGTCAGCATCTTGTATTGGTTGCAGCTGTTTTTTGTGATTTGAGCAGGATGATTGGGCATTCAATTGTTTTTATGAATCTTCAGATGGAAAAAAACAGAATTTTGAAAATCTCTGCAGCACTATAATTCCTTTGTGCTGTTATCATTAAAAACACAAATAGATTATAGGTATCAAACTTGTAAATGTGCCTTAATTAAGCCAAATGCAGTGATGTGTAATGTGTGAATGTACATTTAGGAATATGAGAAGAAACTGGCGAGGCTGCAGGCAGAGTATGATGCCGAACAAGAGTCTAAAGTCAAACTCCAGGAGGACATCGCTGCCTTGAGAACATCATA[T/A]GAGACCAGGCTCTCTTCTTTAGAAAGGTCCAGAGGTAGTCGAACACACACCACTGGTAATGTTGAAATTTGATGTCCTTAGGTCAGTCTTTTGGTTCTGTATGTTATTGATCTGTAGAATCTTGTCGTTCTCTTAAATCAGGTGGTGTTCATCTGCAACAACATAAAGAAGAGCCCATCACTGCATCTGCGGCTTCACAAGAACAGGCTAAGATTGACCACAGTGAATCTGAGGTGTTTTTATTTCGCATTAGTAAATGTATTTAACATTTTTAAAATGTTTTTCATCTGCATATTTAATGTTGTTTAATGACTTCACAAATATAAATGACCCTTTTGTTTAGGAGAGACCGTCTTCTGTTGATGCCACTGTCAAAGGAGCTGCCAGTGGAGAAAGTCAAATTTTAGATTCGGTTGTAGTTGACATACCAGGTCAGCTGGACCAGAAGCTTGCTTTGGAGAGGTGAGATGCTTAACTGGCCTTAAAGTTGTGACTGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa256
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129918 | Nonsense | 553 | 823 | 10 | 14 |
ENSDART00000129918 | Nonsense | 553 | 823 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 38836620)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37403639 |
GRCz11 | 11 | 37670844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGGAGTTTGTGGGTGGCGAGCAGGTGAGGAACGAGGAGCTCAAGCAG[A/T]GACACAAACAGAGGAAGACTCTGGCCGACCAGAGGAAGAAGCAGCTGATC
Long Flanking Sequence:
ATCGTTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTCAATGTCACTAAGCTGTATAGAAGTGTCTTGAAAAAGATCTAGTAAAATATTAATCACTGTCATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTTGGAAAGGTGTTGAAATAATCTGCTCTCCATTAAACAGAAATTGAGGGGGAAAAAAACAGGGGGGCTAATAATTCTGACTTCAACTGTATGTGTATATATTATCCAGTTATGAGCTTGAATGTCATGTAAGTCATTTGCATTTAGCGCCATATATCAGATTCTATGTGGGGAAGAAGAATGATTTATCTGGATATTAAATATGGAGGGCTGAAATGCTGTCTCTGATCATTTATGTTGTCTGAAGGCTGCAGCAGCTGGAGCAGGAGTTTGTGGGTGGCGAGCAGGTGAGGAACGAGGAGCTCAAGCAG[A/T]GACACAAACAGAGGAAGACTCTGGCCGACCAGAGGAAGAAGCAGCTGATCGAAGCTCTGAACCAGAGCAGTGAAGATGGTGACAGTGTGCTGCTGAACGTATACGACTCCATTCAGGAGGAAGTCCATGCCAAGAGCAGACATCTGGAGAACACGCAGAAGAAGGTTTGAGCTTTCGGTACTTCAATATTACTTTTGACTGTTCCCTAAAGGGGAAATTAAGCACTCAGTCAAGTTTACATTATTTTGTACATTGGATTCCACTTGAATGAAAATATATTAAACTCGTTTAATGTTACTGTTTAGAAGAAAACGGCATGTTTTACTATAGATTTTAGACCTAGGGCGCCGCCATCTTTGAATGTCGCTGTGTCTGACGTCACAGGGTTGGTTCCGTTCCCTCAGCTGAACAGATACAGTGGAAGGAGACTGTAAAGACTAATTTAACCCAATGTGTGAAGTTGTGGACGTGGAGCTGGTGCAAATACAAGCGTCAGATGT
Associated Phenotype:
Not determined