ZMP
kif26aa
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate kinesin family member 26 [Source:UniProtKB/TrEMBL;Acc:Q5RIG4]
Human Orthologue:
KIF26A
Human Description:
kinesin family member 26A [Source:HGNC Symbol;Acc:20226]
Mouse Orthologue:
Kif26a
Mouse Description:
kinesin family member 26A Gene [Source:MGI Symbol;Acc:MGI:2447072]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32294 | Nonsense | Available for shipment | Available now |
sa16496 | Nonsense | Available for shipment | Available now |
sa11439 | Nonsense | Available for shipment | Available now |
sa9495 | Essential Splice Site | Available for shipment | Available now |
sa16695 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32294
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 |
---|---|---|---|---|---|
ENSDART00000002641 | Nonsense | 204 | 1906 | 3 | 15 |
ENSDART00000136251 | None | None | 1599 | None | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 27507178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 27578481 |
GRCz11 | 20 | 27477571 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGCCCACGCTATGTCCTCCAGCCGTTGGCAGTCAAAGCCTCAGCAGG[C/T]GACCATGTGGCCCGGAGAATCAAGATGGAGCGGTCAAAGTAGGTGGCAAA
Long Flanking Sequence:
AATCAAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAATCTCTCCATCAAACAAGAATGTGAATAAACAGGGTGGGGGCTAATAATTCTTCAACTGTATATATATTTTCTTGTTTCATTGAACTTTCTGCCTTTTATTTCAGGACCCGAGTTTTGCAGCGTTTCTCCTCGACGAGCTCCAGTCTCAGGAATGGCCTCGGCGGGTCTGCAGTGCCCAGAGCAGCTGTGAAGTGTGTGGGACGTCGCTTTACCACCTGAGGTGCCTGGCACTGCACTCGGCCCTCGGGCTGCCATTCGACAACATGCCTGACCTGCAGCCTGGACCCCTCACTGGCCTTCTGCCTCCACGCGTGGCCTCTCACAGCTCCATATCACCCTATCCATCCTGGGACTGGCCCACGCTATGTCCTCCAGCCGTTGGCAGTCAAAGCCTCAGCAGG[C/T]GACCATGTGGCCCGGAGAATCAAGATGGAGCGGTCAAAGTAGGTGGCAAACGCTCCTGTCTGGCCACTGTCACACCTCTACCTCTACACGCACAGCATTATTTGGAGGGAGTGTGGCGTGTCACAACCGTCCCAGAACACTCAGTGGTAAGAATGAATTTTATATTTATTCATTCATTTTTTTTTTGTTCTGTTGTGTAAATAAGTGTTCAGCTGGGTGTAAATGTTATTGGTATTTATTTTTTTATTTTGATTGCTTCTGCCTTGACCGCTGTTGACTGAGTCTTAAATTTAATCTTTTTCAAAATTAGTCTATAAACCTTTATTTTTTTATTTTATCCGGTTACTAAAATGCTCTATTCTATATTCCCGTCCATCCATTTCACATGCCAATTCATTTATCCATCCATCCATCCATCCTTCACCCTATCCATCCACCCCAATCCAATCCATCCATCCGTACCAATCCATCAATCCATCCATCCATCCATCCATCTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16496
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 |
---|---|---|---|---|---|
ENSDART00000002641 | Nonsense | 318 | 1906 | 5 | 15 |
ENSDART00000136251 | Nonsense | 11 | 1599 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 27549065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 27620368 |
GRCz11 | 20 | 27519458 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTGCCACTGTTATGCAGGGCTGCCCAGAAGCTGAACCTCTCCAAACGG[A/T]AGAAGCCTCAGCCACTTCCGCCATCTCCTCCGGACCCAGAAGAGCCGTTC
Long Flanking Sequence:
GTTTGTACCTTCTTTGGTACAACATTGTACCATTTTTTTTTTTTTTGAGTGTTGAAAAGATGTTTTAGATTAAGTCATCACACAAGACAGTTGCGATCTGTTTTGCTTTGGCTGGTAAAAAAAAAAAAAAATAATTGAACTACCATTAGTCTGTGGCAATGGCATACAGTAATAGTTTGATTTGACCTTCTTTTAGTAGTATGTGTATTTTTCACATTTAGTTATTCATCTAAATGCTGCTCTCAGTAGTGTGGGCAATGATGGAATATTTGCTAACTTTATAGTGCGTGTAGTTGTAAGTTATTTTCACTCTTAAATAAAAAAAGGCTTTTATTTTAAGTATATTAAATCCCACACATAACTTTTATGTGCTCATAATCTTTTAAAATATATACTTAATATCATGTTCAATACAGGATGAACATGTGACTTCTTTTCGCCTAACTTTCTGCTTGCCACTGTTATGCAGGGCTGCCCAGAAGCTGAACCTCTCCAAACGG[A/T]AGAAGCCTCAGCCACTTCCGCCATCTCCTCCGGACCCAGAAGAGCCGTTCTTCTACACTGATGGCTTCAGTGCCGCCCTGCAGCTCTCTCCCCCAGCTGTACCCCCGTGTCTCCTCAGGGCAGGGGCAAAGGTTAAGGACAGCCCTGGGATGGGAAAGGTATGCTAAAGTAATTTTTACCAATATTTGAAAAGTAATCTTTTTTTTTGTTCGTTATGAATTGTTCCGATTTAGAGGCTTTTAGATGGAGCAGGATCAAGGTAATCTTGAAGCCATGCCAACAAGATATTTTATACCATTTAATCAGTGCTGGTACAACAGACAAGTTGTAGTCTGTTAATAATATCTAACTACAATGACATTTGAAGTAAGAAGCATCATTAAGATTACACAGATCAGGTAGTGCACTTTTAGATTAGTCTTGTATTACTTTTGACAAATTTTTCACATTGTCATGTTTACTAACGATCTAACCTTCATAGATCGCTGGAGAACATTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11439
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 |
---|---|---|---|---|---|
ENSDART00000002641 | Nonsense | 638 | 1906 | 10 | 15 |
ENSDART00000136251 | Nonsense | 331 | 1599 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 27567344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 27638647 |
GRCz11 | 20 | 27537737 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCTGCATCTTCTGGACTTAGGAAGTTGTGAGTCTGATCTGAGTCAAACC[C/T]GAGATGGAGGAARAGGCCAGTGTTTGTCAYTAGGTGCCCTTGGAAATGTC
Long Flanking Sequence:
GTTTGTTGTATAGAGCCAAAATGTTTGAATTGTGTCGATGTCCAAATATTTATGGACCTAACGGTTTATCTTGGTTATGTAAAGAGTGTTAAAATTAAGATATGTGCCGTCTGCTCTAACTATTTTGCATAAAAAAGATGTGTAGTAGATATCTAAACATAGATATATACATTCCTGTATATTTAATTACTAGTCTAGATTTGGACTAGTCTTAGATGTCTTTTAGATTTTTGGCTACAGCCCAAATTCAGCCTTGTTTAAGCCAATCTGTCTATGTTTAGACATCTATTGAATTAGCCATTACACACACACACACACACATAAACACACACACAAATGCTTGCTGGGCTGTAAACAATAAAAACTGCAACTAAGAATCATTTACATGGACATTGGGAGTCCTATTTTAACTTGCTGTTTTTGACTTTGCAGTGTCTGGGAATCGTAGTCGCCTGCATCTTCTGGACTTAGGAAGTTGTGAGTCTGATCTGAGTCAAACC[C/T]GAGATGGAGGAAGAGGCCAGTGTTTGTCATTAGGTGCCCTTGGAAATGTCATTTTAGCCTTGGCCAATGGAGCCAAGCATGTGCCATACAGGTATGTACTTTGTTGTTCAATTAATCAATACAAGCCAATAGTGAGAGATGATAGATCTCTGTTAATGGTGGTAATATGTCTAGTGAGTCTTCCTGATCTGCATCTGCAAGGGTTTCATTCTCACCCTCCTGAGATCAATGTAGCCAATTAACCAGCTTCACAGACAGAGAAGGCAGCCAAGTTGAATTGAACTGTGGTGGGATGTATTGATAGGAATGTGGGTCTGGGAGGAATAGATTTATGCTGAAAGGGAATTAAAAAATACTCACCGGAAGGTGGGGTCGTAAATTCAGTGATGCAAGCAGAGAGAATTAATCTTTTTCTTTTAAATGTGGCTTCAGAAAATATCATCCTCCACAACAGAATAAAATAACACTCCAAAAAAGCAGGTCACTAGAAAGTGAGCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9495
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002641 | Essential Splice Site | 668 | 1906 | 11 | 15 |
ENSDART00000136251 | Essential Splice Site | 361 | 1599 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 27567991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 27639294 |
GRCz11 | 20 | 27538384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCCTGGCTTCCTTTTTGGCTAACGAGGAGATTTTTTGATGTATAATTC[A/T]GAGACAGCAAGCTTACCATGCTGCTGAGGGAATCGCTGGGCAACATCAAC
Long Flanking Sequence:
TCTCTGTTAATGGTGGTAATATGTCTAGTGAGTCTTCCTGATCTGCATCTGCAAGGGTTTCATTCTCACCCTCCTGAGATCAATGTAGCCAATTAACCAGCTTCACAGACAGAGAAGGCAGCCAAGTTGAATTGAACTGTGGTGGGATGTATTGATAGGAATGTGGGTCTGGGAGGAATAGATTTATGCTGAAAGGGAATTAAAAAATACTCACCGGAAGGTGGGGTCGTAAATTCAGTGATGCAAGCAGAGAGAATTAATCTTTTTCTTTTAAATGTGGCTTCAGAAAATATCATCCTCCACAACAGAATAAAATAACACTCCAAAAAAGCAGGTCACTAGAAAGTGAGCATCAAAAGGAGGGATATCTTTTATGCAAGTATGATTCATAATCCTCTATTTTAAGACAACCTATCAATGATCTTAGAGGGAATGGGGCTGAATGTTGTAAGGCCTGGCTTCCTTTTTGGCTAACGAGGAGATTTTTTGATGTATAATTC[A/T]GAGACAGCAAGCTTACCATGCTGCTGAGGGAATCGCTGGGCAACATCAACTGTAGAACCACCATGATCGCCCACATCTCTGACTCGCCAGCCAATTATGTTGAATCTCTCACCACTGTGCAGCTTGCCTCCCGTATTCACCGCATGAGAAAGAAGAAATCCAAGGTACTTGATTCATACTGATATATTGCTCATTCAGATTGTATATGCTTATGTAAAAATGTCTTTATAAATGTCAAAAATAACTTTAAGACAACACATTGGGTACAGTGCACTAAGCATTATTCTAAAAGTTAAAATTAAGAAAAATATTTTTATATAATTCAAATAATTTAGACCAATAATTATTTTGAAAATGGTTTACAATTAATTGTTGTTGTCAGCATTTTGTCCACACACACACACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16695
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002641 | Splice Site, Nonsense | 723 | 1906 | 12 | 15 |
ENSDART00000136251 | Splice Site, Nonsense | 416 | 1599 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 27568996)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 27640299 |
GRCz11 | 20 | 27539389 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTGCACAGATATATTTATGTSAGTGTTGTGTGTTATTCTSTTCAGTA[T/A]GCATCAAGTTCCTCTGGAGGGGAGAGCTCCTGTGAAGAGRGACACATCAA
Long Flanking Sequence:
ATATATATATTTCTTTTTTTTCTTTTTTTCACATTCTGCAATACATCAAAAATGGTAGATGAGCCTTTTATTTGTCAGGATCATTCACAATTTAAAAAATAATTTGTGTTTTGTCAGAGGCACAAATGTCAACGTGATAATTACACTGCAAAATTTCTCAGTGACCTATGTCATCTAATCAACAAATGTAATCAATGCAATTTTTCCAGAGGGAGAACAGCATGTAACCTTTTCTATCACAGAGGCAATTTTCACCATAATTACCTGTTTTGACTGAATATATTAATATTTTATAGAACTAAAAATAACCTTTTTTCCTGCATAGCTTATGCATTGCATTGACAATATATTTTATTATTGGTGTGTACTTAATTAATACTGTTAATATTGGCATGCTGTTTCAGTTTGCAAGTGGAATGTCTCTGAATTTATTGCGTGCTGTGAAAGAGGTGTCTGCACAGATATATTTATGTGAGTGTTGTGTGTTATTCTCTTCAGTA[T/A]GCATCAAGTTCCTCTGGAGGGGAGAGCTCCTGTGAAGAGGGACACATCAAACGAAGACCCTTCCACCCTCGGACTGTGGCTCTTGACCCAGACCACCCTGCAGTTTTATCCAGTGATCCAGATTACTCATCCAGTAGTGAGCACTCATGTGATACAGTGATCTATGTTGGGCCTGGTGGGGCCCCTATCTCTGACCGCGAACTCAGCGACAATGAAGGTCCCCCAGCATTTGTTCCTATCATTCCCTCCCTGAACAAGAAGCGTGTAAAAGAGGGATCTAAATCTGATGGGGATCACCTCAAATGTAACACCTTTGCGGAGTTACAAGAACGACTAGAGTGTATTGATGGCAGTGAAAGCACATCTGTTTTCACCAGTGAAGCAAAAGTCCTGCAAACAGCCTTAAAATCTGGAGCGGACAAAGCATCAGAAGGCATTACCTTATTGACAAGGACTGCTAAGTCTTCTCTTCAAAAGCCTACAAACTTGGGAGCTACGTC
Associated Phenotype:
Not determined