ZMP
zgc:56231
Ensembl ID:
ZFIN ID:
Description:
kinesin-like protein KIF20A [Source:RefSeq peptide;Acc:NP_998353]
Human Orthologue:
KIF20A
Human Description:
kinesin family member 20A [Source:HGNC Symbol;Acc:9787]
Mouse Orthologue:
Kif20a
Mouse Description:
kinesin family member 20A Gene [Source:MGI Symbol;Acc:MGI:1201682]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41054 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13283 | Nonsense | Available for shipment | Available now |
sa38646 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21104 | Essential Splice Site | Available for shipment | Available now |
sa38647 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15763 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41054
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024185 | Nonsense | 155 | 810 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 59997768)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58450206 |
GRCz11 | 7 | 58752646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAATGCATTAGTGTTCAGTTATGGAGTGACCAATGCTGGAAAAACATA[C/A]ACAATACAAGGTAAACATGGACATCCACAAAATTTGCTATTTTGGGGAAA
Long Flanking Sequence:
ACAGGTAAAGTTTTATAAAGGTATTAATCTTTGAATTGGTCCTTCAATTGCTTTATTGTAATTGAGGTAAAGTTAGTTTTATATTCGCACGTTCCTTCATTTAATGTTTTCTATATTTTCTGCTACGCTAATTTAAATGTAGGGTCTGAAATAACATGCAAGTATGACTTGAAAACAACATTAGCACTATTTAATTGGCCGTGAACAATGTTGTACTTTGGTATTCATTGGCTGCTAATATGATTTTACTGTTTAGAATTGGCAAATAATACTTTTCTGAAATTATATTATTAATGAAAAGTCTAAATGTGCAAATATAAAACCAACTTTACCTCAGTCTTATTGTATACCAATTTTTGTAATGAAATGCAGATCTTTGGGCCAAACTGTAATCAGACCGAGTTCTTTGAAGGCACAATTAGTTCACAGGTTCAGGCCTTTCTTCATGGCAAAAATGCATTAGTGTTCAGTTATGGAGTGACCAATGCTGGAAAAACATA[C/A]ACAATACAAGGTAAACATGGACATCCACAAAATTTGCTATTTTGGGGAAATGTTCCATTGCATAATTATACATGAGATGGTTTGTTTTAAGGTTCTCCGAAAGACCCAGGCATTTTGCCACGTGCTTTAGAGGTTCTGTTCAAGCACATTGGTGGCCGTCAGTATGAGCACATGGACCTTAAGCCATACTTGAGCTCTGATGTGCAAAAACTGGACTCTGAGCTGGTCAAGCTAGAGAGGAATGCCAAGGCTGCACTCTTCAGTTTGCTTAAAGAGGTTTGCAATCACTCTTAAAATTTCTTAAATGGGGGAGTTTACTAATGTCTGCACTGTCACTAATTAATTTAAGAGTGGACTACTGTGTGTTTACATGACAATGTACTAAAAACAGTACGATTTTGTCTTTTTGAATGTGTCAGTACACACAATTCTGTGAAAACTTCTACAGATGCCAGTGTTGGAATAGCTAGCTACAAGTATAATTTTTAATAGCTTGACCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13283
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 |
---|---|---|---|---|---|
ENSDART00000024185 | Nonsense | 289 | 810 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 59998923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58451361 |
GRCz11 | 7 | 58753801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATCTRCAATGAGCATGTGTATGACCTGCTTCAGCCAGCCCAGTCCAGC[A/T]AAACCAAACGACGTGCTGCACTGAGGGTTTGTGAGGACAGTACAGGGAGC
Long Flanking Sequence:
TTTTACACATTACTTTTAATTTGTAAATATTTTAATTAAAAACAGTTAAAATTCAATCCATAGTGTACTATAACAGTTGGCAATTATCCTGTCTTGAAGAAAGTGTTGTGCCAGGGCTTCAATAAATTAACAAAACGGAGTAAGCCTTTTGTGCGCATTTGTAGTTTTCAGTATAATTGCTTATTGTATACAAAATTTAACTAATTGTTTGTCCTTTTTCTTTTAGGATCCCGAACCCACAAAACTTAGAAAGAGAAGCTCGACATCCTCAATCAATAGTTTGTCATTTTCCAACGTTTCATATGACCATACAGGTATTAAAACATTCTGATCAATAGATGGTTTGCATAACTGTTGTATAAGCTTTTAACCAATGTCTTCCAGTTGACAGTGCTGATGGCATGGCTGATGAAGCACATTGTTTTTACTCTGTTTGGGTGGCGTTTTATGAAATCTACAATGAGCATGTGTATGACCTGCTTCAGCCAGCCCAGTCCAGC[A/T]AAACCAAACGACGTGCTGCACTGAGGGTTTGTGAGGACAGTACAGGGAGCTCATACATTAGAGGTGAAGCCCTTTCACTCTTGAAGAAGCAAAGCAAATGTTTGAATGCACTTTTAAATTATGTTTGTTACTTTTGGAAGATTTAAGGTGGGTTAATGTGCAGAATACAGAGGAGTTCAGTAAGGTTCTGCGTGTGGGCAATAAGAATCGGAGTGCAGCAGCGACCAAGATGAACCAGTCATCCAGCAGAAGGTAGACTTCCCTATCTGCTAGTTTGATTCTTGATCTGGTTTGCAAATCTAAAGAAGGTTTTTACATGACAAACATTTAGTACATGATTAACCTTTTAGTTTTTTTTTTTTTTTTTTTTTGCAGTCACAGTATCTTCACCATCAAACTGATACGCATTGAAGGAGCAGACGTTCAAGCATTGTCAGAGTAAGTGGAAAGAGCGCATTATTTGTAACGCATGTAGTTTTGTAAGTGTAACATGTTTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38646
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024185 | Essential Splice Site | 368 | 810 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 59999363)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58451801 |
GRCz11 | 7 | 58754241 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCAAACTGATACGCATTGAAGGAGCAGACGTTCAAGCATTGTCAGAG[T/A]AAGTGGAAAGAGCGCATTATTTGTAACGCATGTAGTTTTGTAAGTGTAAC
Long Flanking Sequence:
GCGTTTTATGAAATCTACAATGAGCATGTGTATGACCTGCTTCAGCCAGCCCAGTCCAGCAAAACCAAACGACGTGCTGCACTGAGGGTTTGTGAGGACAGTACAGGGAGCTCATACATTAGAGGTGAAGCCCTTTCACTCTTGAAGAAGCAAAGCAAATGTTTGAATGCACTTTTAAATTATGTTTGTTACTTTTGGAAGATTTAAGGTGGGTTAATGTGCAGAATACAGAGGAGTTCAGTAAGGTTCTGCGTGTGGGCAATAAGAATCGGAGTGCAGCAGCGACCAAGATGAACCAGTCATCCAGCAGAAGGTAGACTTCCCTATCTGCTAGTTTGATTCTTGATCTGGTTTGCAAATCTAAAGAAGGTTTTTACATGACAAACATTTAGTACATGATTAACCTTTTAGTTTTTTTTTTTTTTTTTTTTTGCAGTCACAGTATCTTCACCATCAAACTGATACGCATTGAAGGAGCAGACGTTCAAGCATTGTCAGAG[T/A]AAGTGGAAAGAGCGCATTATTTGTAACGCATGTAGTTTTGTAAGTGTAACATGTTTCTCTTCTCGTGTAGACTTTCTCTTTGTGATTTGGCTGGCTCTGAAAGATGCAACAAAACTAAAACCTTTGGAGATCGACTAAAAGAAGCTGGTAACATAAACAATTCTTTGTTGATTCTGGGCAAGTGTATTGCAGCACTCCGGAATAACCAAGGTTTCAGGTATGGGCAAATACCAAATGGAACCGAAAAAAAAAAAGCAGGTTTATATGTGCTGACTTCGTGTTCGTTTCTCAGGACAAAGAGTTATGTTCCATTTCGAGAGAGCAAACTGACACGGCTCTTTCAAGGAATGTTTTGTGGCCGTGGCAGGGCTTCCATGATTGTGAACATTAATCAGTGTGCCTCAACATATGATGAGACCCTCCATGTGATGAAGTTTTCTGCAGTTGCCAAGCAGGTTTGCTTTTTTTTTTTTTTTTTCATTTTTATACCCCCTCTTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21104
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024185 | Essential Splice Site | 530 | 810 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 60001453)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58453884 |
GRCz11 | 7 | 58756314 |
KASP Assay ID:
2259-9633.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCTGCTGGATGGAGATGAGGCAGATATGTCCATATTACCCCAAGAGG[T/A]AATTTATTGCTTTGGTTGAACACTTGCATTAGTCATGACATTGAGAATAT
Long Flanking Sequence:
ACTGGCCACTTAAAAGTATTAATACTTAGTAACTATAAATACTTTTTTGTAGAAGGCTTTAATTAGGAGCAAAAACTATGTGCTGTCTGTCAGTACATTAATATTGCATTAAATATGCATGCTGCTAACGGACAGCCAATTGGTACAATTTGGGTTTGTGGGATTTTTAACCTGAAATAAAGTCTGCTCTGGAGCAGTTTATTCATGTAGCGCAAATGGCCTTGGTGACTACCTGGTTACTCACCTTTTTGTGCCTAAAAACTTAATACTTAATATTAACTGTACCTGGATTAAAACCATCTGGGGCCTGTATACATTTTAGGTATTACAGGTGATTCCTCCAAGATCTCTGGAGTCTCTGGCACCACGTATTGTTGGTCTGGATGGGAAGCCATTGCTAAAGAATGGCGTTATTGATGATCAGGCTGTAGATGATTACCTATCGGAGGAAGAGCTGCTGGATGGAGATGAGGCAGATATGTCCATATTACCCCAAGAGG[T/A]AATTTATTGCTTTGGTTGAACACTTGCATTAGTCATGACATTGAGAATATAGTGTTTGTGTACCCAAAAAGCAGAGCTCAACAATTTCAATGTAACTGAAGTACTTGTGGAGAAACCCTTGCAACTTTATCATTTAGATTGTTTGTATGGCATTCTCTTTCAGGAGTTGGTGAACTTGGTGGAGAGCTTGCGTGTAAAGCTCTTGGCAGAGCGTAGAAAAAATCTGTTGCAAGAAATTCAGATTCGTAAGGAGATGGGTGATGCGATGTTGCAACAAATCATGGAGGCAGAGGAGCTGCACAGGTATGTTTTTGTAAATTAGTGATTAAGTCACCTTAACACATTTGTGGAAGGTTATTCACTTTTATTCGCGTATGTGTAAAGTCGTCAGATGGAAGATCTAAAGGAGAGTTATGAAGAGAAAATGGACAGCACTTTTGAAATGTATAAAGAGGCATTGAAGGAGCATGCATACCAGTGTGCTCTGGAGAGACTGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38647
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 |
---|---|---|---|---|---|
ENSDART00000024185 | Nonsense | 717 | 810 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 60002532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58454963 |
GRCz11 | 7 | 58757393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCGGATAGGAGAGTTGAATGATACTCTGCAAGAAGCGGGGGAGAGTTA[T/A]ATGGAAAAACTTGCAGAAGTTCAAAATCTGCAAAACAGGCTATCAACTCG
Long Flanking Sequence:
TGATAATGAAATCCTAGAATTGTAGCTGTGTACCACAAAAAATAACTCAAGCCTAATTTATTAAACCACTCTGGTGGTGTTTTTTTTTTTAGGTGCTAGAGAAGCGTGTATGTGAGTTGGAACAGAAATGCCGGTGTTCTGGTCCTCTACCCAACGTACAAGACAACTCCATGCAGACAAACGCACTGCCAACCACAGAAGCGTCAGGTATAAGAGAGTGTGTGTGTGCTTTTTAAACATTAAATTTTTTATTTGGTCAACTCATGCATGAATTGCCCATGCAGGTGCTGAAAGGTTTAAACTGCTGTACAAGGAAAAGTGTGCAGTTGAGAACCTCTGTGTTGAGAAGCAAGAGGTAAATGGACTTGTGACGACTTCTGTTCTACAACTTTCATTTTTACAACTCGTTTTATTATTATTATTTTTTTTTAGTTCATTATGTCTCTTGAGCAGCGGATAGGAGAGTTGAATGATACTCTGCAAGAAGCGGGGGAGAGTTA[T/A]ATGGAAAAACTTGCAGAAGTTCAAAATCTGCAAAACAGGCTATCAACTCGGGTAAGAATGCATGCAAGTAACTTTGTTTGGCTATGTGCTTGTTATGAACGCTTTTATTTATTGCTGATAGGAGCAAGAGATTGAATGCTTGCAAAGTAACATCATGGCTAAAGAGAAGGAGATAACTGGTTTGCGGGAGGAGATCACAAAGTTGGCCAGTGATTCTATAGGACCACCTCGTTCAAGGTGTGGTCTGTTGGTCAACATTAAAGAATCAATGACTCCTCCATCTACAGGAAGTTTATGCCGCACTATTAGAAAGTCTGTGAGAGCAACATCTCTAAGGAAAAAGGCGAGCTGATTGCATCCTGGAGCTCTTTTGTAGCACTTTGTTTTTACCAGGTTTTTAATTCAATAATAAATGATCTTTTTAATTTGACTTTTTTGTGTGCCTTTTGCTGACTGCGTAATGTTTACTTCCCATATGAGATTTGTATGAAATATGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15763
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024185 | Essential Splice Site | 734 | 810 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 60002584)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58455015 |
GRCz11 | 7 | 58757445 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAAAACTTGCAGAAGTTCAAAATCTGCAAAACAGGCTATCAACTCGG[G/T]TAAGAATGCATGCAAGTAACTTTGTTTGGCTATGTGCTTGTTATGAACGC
Long Flanking Sequence:
CTAATTTATTAAACCACTCTGGTGGTGTTTTTTTTTTTAGGTGCTAGAGAAGCGTGTATGTGAGTTGGAACAGAAATGCCGGTGTTCTGGTCCTCTACCCAACGTACAAGACAACTCCATGCAGACAAACGCACTGCCAACCACAGAAGCGTCAGGTATAAGAGAGTGTGTGTGTGCTTTTTAAACATTAAATTTTTTATTTGGTCAACTCATGCATGAATTGCCCATGCAGGTGCTGAAAGGTTTAAACTGCTGTACAAGGAAAAGTGTGCAGTTGAGAACCTCTGTGTTGAGAAGCAAGAGGTAAATGGACTTGTGACGACTTCTGTTCTACAACTTTCATTTTTACAACTCGTTTTATTATTATTATTTTTTTTTAGTTCATTATGTCTCTTGAGCAGCGGATAGGAGAGTTGAATGATACTCTGCAAGAAGCGGGGGAGAGTTATATGGAAAAACTTGCAGAAGTTCAAAATCTGCAAAACAGGCTATCAACTCGG[G/T]TAAGAATGCATGCAAGTAACTTTGTTTGGCTATGTGCTTGTTATGAACGCTTTTATTTATTGCTGATAGGAGCAAGAGATTGAATGCTTGCAAAGTAACATCATGGCTAAAGAGAAGGAGATAACTGGTTTGCGGGAGGAGATCACAAAGTTGGCCAGTGATTCTATAGGACCACCTCGTTCAAGGTGTGGTCTGTTGGTCAACATTAAAGAATCAATGACTCCTCCATCTACAGGAAGTTTATGCCGCACTATTAGAAAGTCTGTGAGAGCAACATCTCTAAGGAAAAAGGCGAGCTGATTGCATCCTGGAGCTCTTTTGTAGCACTTTGTTTTTACCAGGTTTTTAATTCAATAATAAATGATCTTTTTAATTTGACTTTTTTGTGTGCCTTTTGCTGACTGCGTAATGTTTACTTCCCATATGAGATTTGTATGAAATATGTTTGATATTTATTATTTTTCCAAGTTGTTTAAAGGAACAGTGAGTTTTGTAGCTAA
Associated Phenotype:
Not determined