ZMP
si:dkeyp-8f4.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RHQ6]
Human Orthologues:
KIF26A, KIF26B
Human Descriptions:
kinesin family member 26A [Source:HGNC Symbol;Acc:20226]
kinesin family member 26B [Source:HGNC Symbol;Acc:25484]
kinesin family member 26B [Source:HGNC Symbol;Acc:25484]
Mouse Orthologues:
Kif26a, Kif26b
Mouse Descriptions:
kinesin family member 26A Gene [Source:MGI Symbol;Acc:MGI:2447072]
kinesin family member 26B Gene [Source:MGI Symbol;Acc:MGI:2447076]
kinesin family member 26B Gene [Source:MGI Symbol;Acc:MGI:2447076]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9753 | Nonsense | Available for shipment | Available now |
sa37105 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37104 | Splice Site, Nonsense | Available for shipment | Available now |
sa6641 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23759 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9753
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037195 | Nonsense | 54 | 1464 | 2 | 13 |
ENSDART00000131919 | Nonsense | 15 | 1456 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 35064608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35137121 |
GRCz11 | 20 | 35040000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTTCACAGGGCTGCACAAAAGTTGAATGGGATGGTCAGGAGAGGAAGGT[C/A]GTTCTCAGAAAGCGGCGCTTCTCCACATCTGACAAACTTCAGTGGTGTCC
Long Flanking Sequence:
TAAGCGTACATATCGGCCTCTGGTGGACAAAAACTGCAAAAAACGTACCTGCTGGGATGTATTTGGCGCTCTCCAGAAATGTATATAGGAGTATGTTTTCAGAATGAGCCTGGGTTGTATTTTTTTGTGGATGACCTGAATATGTATGAAGTTTCAGCATATTTAATTTTTTTGTAATTACTAATCGACAGTCTCAGTGACGATAAATCTCTCTCAGTCTTCCCAGAGTCCTTCACATTCAGGAAAGGTGTGTGAGAAGGAGAACATGACCTCTACAGCTCTGTGCAACTACAGCCCGTCACGGCCGTCCCGTTCATCCAGCATGTCTTCTCTGCTCCCCGCTGGAACCTCCGCCGCCTTGTCCTTCTTTGTCAAGTAAGCGCTTCTAAAAAAAATCTAATTAAAAATCAACCAAAAGGATCATGGTTTAAGCTAAACTAAATTATTGAACGTTCACAGGGCTGCACAAAAGTTGAATGGGATGGTCAGGAGAGGAAGGT[C/A]GTTCTCAGAAAGCGGCGCTTCTCCACATCTGACAAACTTCAGTGGTGTCCTGCAGAAATCTCCTCCTCAAGCACCGGCCAGCATCTTTCAAACCGCTGGGAAAGGCAAGGAGACTTCTGGGATGGGAAAGGTATGTCTGAACGCTCAGAATTTTGGTTGTTATTTAATGTAAAGTAGTAATAAAACATCAAACAATGTATGGGTGATTAAACAACTATTAAGCACCGTGTTATGTGTGACAATAGCATTTTTTTTACTCATTTCAAAAATATGTTTGTTTCATTATTATTCATGATTCATGATTATATTTCACTTACTTTTTGTAGTTAAATTGGCCAGTATAATTTTGTTTAATGCTGTAAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAACATAACATAATATAATATAATATAATATAATATATACAGAAATAAGACAGATATATATCTGTCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37105
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 |
---|---|---|---|---|---|
ENSDART00000037195 | None | None | 1464 | None | 13 |
ENSDART00000131919 | Nonsense | 517 | 1456 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 35044332)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35116845 |
GRCz11 | 20 | 35019724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCCACCAATTGGCAATCGCATGAAGCAGATATCAAAAGAAAAGGCC[A/T]AAGAAGAGCCAACACCAACAATATTGCAAAATAAATCAGATTTTGAGTGT
Long Flanking Sequence:
AATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATCGTATTGTCCTGTTTTTGAATGCAGTGAATTAAGGTCTAGTTTTACTTTTACTTTTTTTTTTTTACCCAGAAATCTTCCTCAAGCTCACCTGGAGGAAGAAGCTTAGGCAATGAGAGGAAAGTTAATAATTCCACCAAAATGAGATTCCAATCGACAGGAACCCTGGATCAAGATCTCTCCTCTCCTGGTTTCTCTAGTGATCCAGCATTTTATCCTGGGAGCGACAACTCTTGTGATACTATTATCTCAATGGATCGGTCTGGCCTCCTGGATAAAGAGGTTACAAACAGAAGCAGAGAGGTTTTACCTATTATTCCATCTTTACTCAAGAACAAATTAGAGACCAAGAAGCTCTCGCTGATGAGGTTTTGTGAAATCTCTCCACCAATTGGCAATCGCATGAAGCAGATATCAAAAGAAAAGGCC[A/T]AAGAAGAGCCAACACCAACAATATTGCAAAATAAATCAGATTTTGAGTGTCTAAAGTGTAACACATTTGCAGAACTCCAAAATCGACTGGGAAATATAGATGGAACAGAGCTGGACCCTTGCAAAGATCAGGAAGTGCATGCCATAAACCAAAACCAAAACCCTCACTTAAATCACGCTGAGAAAAAATCTAATTCATTGGATAATCAAGAGTCAAGCAAATGTGAAGTTACCAGACAAGGAAGCTCATCAAAAACAATTGCCATAATTCACAACAGTGAACAAATTCCATGTACCACCAATTCACAGATTATTAACACATGTCCACAACAGTCACATATTGTCAAACCAATCAATTCCATGTTGTCTAGCCAATCTCCAAGCAAATCTATGCTTTACAATAAAAAAATGGATACGACGCCCACTTCACTACCTTTGAAATTTGAAGACCAAGATAAAACAAGAGTATCAGACGATTCCACAATGCAAACTCAAACACGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37104
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037195 | Splice Site | None | 1464 | None | 13 |
ENSDART00000131919 | Nonsense | 526 | 1456 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 35044305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35116818 |
GRCz11 | 20 | 35019697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGATATCAAAAGAAAAGGCCAAAGAAGAGCCAACACCAACAATATTG[C/T]AAAATAAATCAGATTTTGAGTGTCTAAAGTGTAACACATTTGCAGAACTC
Long Flanking Sequence:
TTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATCGTATTGTCCTGTTTTTGAATGCAGTGAATTAAGGTCTAGTTTTACTTTTACTTTTTTTTTTTTACCCAGAAATCTTCCTCAAGCTCACCTGGAGGAAGAAGCTTAGGCAATGAGAGGAAAGTTAATAATTCCACCAAAATGAGATTCCAATCGACAGGAACCCTGGATCAAGATCTCTCCTCTCCTGGTTTCTCTAGTGATCCAGCATTTTATCCTGGGAGCGACAACTCTTGTGATACTATTATCTCAATGGATCGGTCTGGCCTCCTGGATAAAGAGGTTACAAACAGAAGCAGAGAGGTTTTACCTATTATTCCATCTTTACTCAAGAACAAATTAGAGACCAAGAAGCTCTCGCTGATGAGGTTTTGTGAAATCTCTCCACCAATTGGCAATCGCATGAAGCAGATATCAAAAGAAAAGGCCAAAGAAGAGCCAACACCAACAATATTG[C/T]AAAATAAATCAGATTTTGAGTGTCTAAAGTGTAACACATTTGCAGAACTCCAAAATCGACTGGGAAATATAGATGGAACAGAGCTGGACCCTTGCAAAGATCAGGAAGTGCATGCCATAAACCAAAACCAAAACCCTCACTTAAATCACGCTGAGAAAAAATCTAATTCATTGGATAATCAAGAGTCAAGCAAATGTGAAGTTACCAGACAAGGAAGCTCATCAAAAACAATTGCCATAATTCACAACAGTGAACAAATTCCATGTACCACCAATTCACAGATTATTAACACATGTCCACAACAGTCACATATTGTCAAACCAATCAATTCCATGTTGTCTAGCCAATCTCCAAGCAAATCTATGCTTTACAATAAAAAAATGGATACGACGCCCACTTCACTACCTTTGAAATTTGAAGACCAAGATAAAACAAGAGTATCAGACGATTCCACAATGCAAACTCAAACACGAATATCTCCCATTGGCAAGAGTTCTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6641
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 |
---|---|---|---|---|---|
ENSDART00000037195 | Nonsense | 672 | 1464 | 10 | 13 |
ENSDART00000131919 | Nonsense | 662 | 1456 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 35043896)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35116409 |
GRCz11 | 20 | 35019288 |
KASP Assay ID:
554-4599.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTATGCTTTACAATAAAAAAATGGATACRACGCCCACTTCACTACCKT[T/A]GAAATTTGAAGACCAAGATAAAACAAGAGTATCAGACGATTCCACAATGC
Long Flanking Sequence:
GAGGTTTTGTGAAATCTCTCCACCAATTGGCAATCGCATGAAGCAGATATCAAAAGAAAAGGCCAAAGAAGAGCCAACACCAACAATATTGCAAAATAAATCAGATTTTGAGTGTCTAAAGTGTAACACATTTGCAGAACTCCAAAATCGACTGGGAAATATAGATGGAACAGAGCTGGACCCTTGCAAAGATCAGGAAGTGCATGCCATAAACCAAAACCAAAACCCTCACTTAAATCACGCTGAGAAAAAATCTAATTCATTGGATAATCAAGAGTCAAGCAAATGTGAAGTTACCAGACAAGGAAGCTCATCAAAAACAATTGCCATAATTCACAACAGTGAACAAATTCCATGTACCACCAATTCACAGATTATTAACACATGTCCACAACAGTCACATATTGTCAAACCAATCAATTCCATGTTGTCTAGCCAATCTCCAAGCAAATCTATGCTTTACAATAAAAAAATGGATACGACGCCCACTTCACTACCTT[T/A]GAAATTTGAAGACCAAGATAAAACAAGAGTATCAGACGATTCCACAATGCAAACTCAAACACGAATATCTCCCATTGGCAAGAGTTCTCCAAGATCTACCTCTTCTTCTTCTTTTTCGTCATCCCTCTCTTCCAGTTTGAGCTCCCCAGCTGTTTCTGCCTCTTTGAATGGAGACGTTCCACCTTGTACCTTAAAGAACCAACGAGAAATGAGGGCCACCATTACTGTGACTGTTCAGCAGCCACTGGATCTTAATGGACAAGATGAACTTGTGTATACTGTGGTTGAGGAGGTAACAATAAATGGGGCCACTGATCAAGGAAAGGCAAAAATATTAAGTATTCATGAGTCACACTCTCTCCAGGCTTTAACGCCAGGAAATCAGTCTGTCAGGATTATCGGTAGTGTAGGTGAAGAACAAACAGAGGGTTTTTATAGTTGCACCTCTAATGCACAGACATCAGAGACTGAAATCTCCATGGCCTCGTCTGATACAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23759
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 |
---|---|---|---|---|---|
ENSDART00000037195 | Nonsense | 1430 | 1464 | 13 | 13 |
ENSDART00000131919 | Nonsense | 1405 | 1456 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 35038911)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 35111424 |
GRCz11 | 20 | 35014303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGCAGTTGACTTATGGCAAACCTTTGAGGTAGACTCCCTGGAGCATT[T/A]GGAGGCCTTGGAGGTGGTCACGGAGCGACTAGAGCGTCATGTTAACCTCT
Long Flanking Sequence:
TGTGTAATTCGGTGTATCTGTGTATTTGATGGCTTTGTGCCTCATTTAAAGGCAATATTTGAATTGTTTGTACTATGATATGTAGAATTAAAACAACTGTAACGGTAAACCTGTGGTGTGATGCTAATCTCAGATCACTCACATTTCATATGGAGGGAAACTGACATTTTGTCATCCCCGTTTTCAGGGTGTAGTCCTCTTTAGTGCAAAGCTGAAATTTCTGGAGCATCGACAGCAGAGAATAGCAGAGGTGAGGCTCAAGTATAGTGCTCTCAAGCGGGAGCTGGAACATGCCAAGCATCATCTGATGTTGGACCCTGCAAAATGGACCCGTGAATGTAAGGGTTAAAATATTGCTCATGCATAATAATAAATGTTAAGAACACTGTAGGGAATCACAAACTCCAGATTGTGATTATTCATTAATTATGATGCTGTTTGTTTCATGTATTTTGCAGTTGACTTATGGCAAACCTTTGAGGTAGACTCCCTGGAGCATT[T/A]GGAGGCCTTGGAGGTGGTCACGGAGCGACTAGAGCGTCATGTTAACCTCTGTAAAGCACATGTGTTGATGGTCACCAGCTTCGATGTTACACCCAAGTGCAGACTAAAGTGGAGGCATCGGCCCACCATAGATCATACTACATTTGTAGGAATTTAGCATGCAGTGTTTACATGTTATGCATTGTTTGAAATTGTATGCAAATCAATGCCTTTAAATGATCTCAAAAGCTTCCATTGGCATTTACTTGAAATTTAATTTGCTGTAAATGGTTTGTGCTGTTAGCATTAGCCTTAAAGCTAACAACAATAGGTTGCAGATACTGTCTGAACTTAAATTGGCTGATAGGCTTTCCACGCCTGAAACTGTTAAGCTATAGGGTGGTGTTTTTGGACAATCGTGTTTTGTTTTTTTGCATTTGTATAACCTTTTTTTGTCTGTAATATAACTGCTTGTATAGGTATTTAATCCGTTTCTCTCTGAAGCATAACTTTATGATTAT
Associated Phenotype:
Not determined