ZMP
kif5a
Ensembl ID:
ZFIN ID:
Description:
LOC553428 protein [Source:UniProtKB/TrEMBL;Acc:Q504B9]
Human Orthologue:
KIF5A
Human Description:
kinesin family member 5A [Source:HGNC Symbol;Acc:6323]
Mouse Orthologue:
Kif5a
Mouse Description:
kinesin family member 5A Gene [Source:MGI Symbol;Acc:MGI:109564]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10562 | Nonsense | Available for shipment | Available now |
sa27306 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7168 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10562
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 |
---|---|---|---|---|---|
ENSDART00000044227 | None | None | 349 | None | 11 |
ENSDART00000110704 | Nonsense | 361 | 1033 | 11 | 29 |
Genomic Location (Zv9):
Chromosome 9 (position 200668)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 283842 |
GRCz11 | 9 | 283475 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAATACGAGAAGGAGAAGGAGAAGAACAAGAGTCTGCGGGACTCCATG[C/T]AGAGGCTGGAGCTGGAGCTGCGGCGCTGGCGCAACGGTAATCACAGTCTG
Long Flanking Sequence:
CCACAAATGTAGACCTGGGTATGTATCCGCAATGAGTCTGTGTTGCACACTTTCACATCCACATGGACATACGGTGGCCGAGACAGCCGAACAGTTTAGGAAAACACACACAAGTGCACAATTCACCAGCAAGTTAAGTAAAGATCCTCAACATTTTGACAGCACACATGTTGCCTTAAGATCAGGCAACCGAAGTAAGAATAAATTAGGTACAAACAAGCTAGTAGTTACTAGGCCTCTGGTTTGGTCCTTGTGTTCAAGCAAGAGTTTACAAACAGCTGCTGCACTCCATATGTGCTTGAAACTGAATAGCAGATAACTGTGGAGTTACACTGCGGTGCTGATTCCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTAGTGCTAAGACCATCAAGAACACGGCCTCCATTAACCTGGAGCTGACAGCGGAGCAGTGGAAGAGGAAATACGAGAAGGAGAAGGAGAAGAACAAGAGTCTGCGGGACTCCATG[C/T]AGAGGCTGGAGCTGGAGCTGCGGCGCTGGCGCAACGGTAATCACAGTCTGCCCTGCTAACATCAGTCCGGCAGATTCCCTGATACAGCACTTTACATAACTCCACCATCACAGCATGTGCTCAGCTGAGGCCAGGGCGAGTCAGCATCGTGAAACCCTTAGCTTAAAGGCATAGTTTGATCAAAAAGTCATGGTCATCTGCTCAACCACAGGTCATCTAAGATGTTTACTGAATTTGTTTCTTCAGTAGAGCATCAAAGAAGATTTTGGGCTGAATACACTGACCTTGATGATTGGAATTACGCCAGTCAATGGTTTCAGTCAAAGCTGTAACTTTGGTTCGAAAAATGCTGGGACACACAAAATGGAAACTATTTTGCTGATTTAAATCCCATTTACAGTTTTAATAGAGAGTAAACTGATGCAAATCACCATACAAGCTCAAAAGGAAGCATATGCAAGGAGAAAATCAAAGGACCTAATACTGAGCCTTGTGGCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27306
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 |
---|---|---|---|---|---|
ENSDART00000044227 | None | None | 349 | None | 11 |
ENSDART00000110704 | Nonsense | 820 | 1033 | 22 | 29 |
Genomic Location (Zv9):
Chromosome 9 (position 211702)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 272808 |
GRCz11 | 9 | 272441 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCCACAACCTGCGCAAGCTGTTCGTTCAAGACCTCACGACTCGGGTT[A/T]AAAAAGTGAGTTCAGCACCTGAACATGGATCATGCGCTGGAGAGATCTTA
Long Flanking Sequence:
TAATGTTTTTGTCTTGTTTCTAGTCCAAATATCAACAAATTATAAAATCAAAAAGCATTTTCTAGACAAGCCGAACATATTGTCTTGTTTTAAGAAATAATGAGTCAAAATGAAGCAATTAAGCAGAATAATCTACCATGAGGTGAACAAAACAATCTTCTGCCAAAGTGAAAACTAGATCATTCAGCGGCTGGTCGACACCTCATGAATTTAAGCTAACAGAACATATCTGGACATGTTTAAAAATGATTGATTCACAACCAAGCGAGCATCAACAATCTACAAGCTCTCACAGCAGCAAAAATCAAACTGTGTATGCCTACTTTTTGGATAGAAGTCGGGAAACAGAAAGGATTAGTCTCAGTTTTATTCCACCAGCGAGTAACAGTGAATGAGAAAGTTCTGGAAAGTGATGTTGAGTTTGTCTTTCGCAGGCTCGGGAACTCCAGACCCTCCACAACCTGCGCAAGCTGTTCGTTCAAGACCTCACGACTCGGGTT[A/T]AAAAAGTGAGTTCAGCACCTGAACATGGATCATGCGCTGGAGAGATCTTATACTGCTGTGTGTCTTTGATTATGCTTCATTTTTCAGTTTAATTCTACATTTAAGTACTGTGGAATATTCATTTACAGCATGCACTTACTAAAGGAGAGTCAATCAGAACAATACACAAGGGTTAATTGGCTGTTAGTGTAAAAGGCAGTGTATAGTGAAGTGTCAGCTCATCTTCTCTTTGCACAGAGTTCAGAAATTGGACCTGATGATAGTGGGGGGTCTAACACCCAGAAGCAGAAGATTTCCTTTCTTGAGAACAACCTGGATCAGCTTACAAAGGTTCATAAACAGGTGAGGACGCTCTGAGGTTACGTTTGTTGGACATATTTCACTGAATCCATGTCATCCCATTATATCCATACACTTCACTGAACATCTCTGCATCGCCTATTTACTATCATAGTGCAGGATAATATGCTTATATATTGTAACTTTAACAGTTAAAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7168
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044227 | None | None | 349 | None | 11 |
ENSDART00000110704 | Essential Splice Site | 929 | 1033 | 24 | 29 |
Genomic Location (Zv9):
Chromosome 9 (position 213503)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 271007 |
GRCz11 | 9 | 270640 |
KASP Assay ID:
554-5350.1 (used for ordering genotyping assays)
KASP Sequence:
GCCATGAGRCTGCGTTACCCACTGCGCCGSCCCAACGCCGCTCAGATCGG[T/C]ACRCTGAACACTGCATTCACATTCACACACACTCTCTCAGATCCTCTTTA
Long Flanking Sequence:
ATGTACAAACATATACACAAGTAAACAAATAGACCAAATGATACGTTAAACATCTGCGGAAATCTGTGTATTTCTGTGCACATGGATTCTGTCTGGCTCTAGTTATTAATAACTAATACAGTTATGGAAACTGATAACCTCAACTTTAACTTCATTTAATTGTAGTAATGTGCACCTTCTGTACAGCATCTGTGAAACAGTAATTGTTATGAAAAGCGCTGTACAGATTGAACTCAATTGAGCTGAGCTGAATTTCCTCATTGCGTCCTCTGTGTCGAGCAGCTGGTACGTGATAATGCAGATCTCCGCTGTGAGCTTCCGAAGCTGGAGAAACGTCTTCGTTCTACGGCTGAGCGGGTTCGGGCGCTGGAGACAGCACTGAAGGACGCCAAACAGGGCGCGATGAATGACCGGCGCCGGTACCAGCAGGAGGTGGAGCGCATCCGGGACGCCATGAGGCTGCGTTACCCACTGCGCCGGCCCAACGCCGCTCAGATCGG[T/C]ACGCTGAACACTGCATTCACATTCACACACACTCTCTCAGATCCTCTTTACAGCGCATTGATGATTGATGATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGCTTTTCTCCCCTCTCAGCTAAGCCAGTGAGACCCGGGCATCACGTCACCGCCACATCGCCCACCAGCTTCTCCGTCACACGCGCTAGCAAACCGGCCACGTCTTACAGCAATGCCCGATTCCTGCAGGACGAGAAGATGGAGAACAGCCAGAAGACCAACACGTGAGCATCTGTCTGTCTGTCTGTCTGTTAGGGGTGTTAAAACTTATCATTTGGTCAATGCACCATGATGCAGATGTTGATGATTCGGTATCAGTTCAGTAATAGATCATAACCAGTTATTACATGCCAAGGTCATTCATCTCTTATGAGCTGTCACGCTAGAATACTATGGCGAGGGAGGCGAACGTAAGTAAT
Associated Phenotype:
Not determined