ZMP
kif5ba
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate kinesin family member 5A (KIF5A) [Source:UniProtKB/TrEMBL;Acc:B0
Human Orthologue:
KIF5B
Human Description:
kinesin family member 5B [Source:HGNC Symbol;Acc:6324]
Mouse Orthologue:
Kif5b
Mouse Description:
kinesin family member 5B Gene [Source:MGI Symbol;Acc:MGI:1098268]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25891 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31295 | Essential Splice Site | Available for shipment | Available now |
sa1774 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa39921 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19854 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25891
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 |
---|---|---|---|---|---|
ENSDART00000113849 | Nonsense | 46 | 968 | 2 | 26 |
ENSDART00000138947 | Nonsense | 46 | 850 | 2 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 43790921)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43876422 |
GRCz11 | 2 | 43729420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGAATGTACCATTGAACCGTGTTTTGTTTTTCTCAGGGTAAGCCGTA[T/A]GTGTTTGACAGAGTTTTCCAGTCCAACACGACACAGGAGCAGGTGTACAC
Long Flanking Sequence:
ATGCTCACAACTTTTGTGTTGCGTTGTACTCGTCTCTCATCAGAAACTGCTTCGTACTATCATGATAATAGGTTTTCAATACTTTAGCTCATCCATTAACATGATTTTTGTGTGATATAATGAAGATGACAACTCCCATGGTATCACACTGCGTCATCAAAATACACCTTTGTTTGTTTTGAACATTCGCCTTCTAGGGGTGAAATTACTTACTGTGCCTTTAAAATCCATTCACCCTCAATGTGGTGTGGTCAGCATAAATGCATAGAGTTCCACAAAACACAATAGCTGATAAATGATACAGTAGTGATGGGTTATGATAGAAATGTATCATGCAACATTAATCATAGTATTACCTTCAAATGATACCTTTGATACAGGATTATTTGCTAATTAGCCAATTGTATTCATGCTGGTGTTATTAATCAACCATACAGATTAGAATTCAATGATTGAATGTACCATTGAACCGTGTTTTGTTTTTCTCAGGGTAAGCCGTA[T/A]GTGTTTGACAGAGTTTTCCAGTCCAACACGACACAGGAGCAGGTGTACACAGCCTGCGCTCAACAGATCGTCAAAGGTAGATGCAAAAGTTCGGTTGATAGACCTCTCAGTCAAAATAAAACCTTCAATAATTTTTAAAACACGGCTGTTTCCACAGATGTACTTGCTGGATATAACGGAACCATTTTTGCCTATGGTCAGACGTCCTCAGGCAAAACACACACAATGGAGGTGGGTGAGAATTGATGTTCAATTGGCTAAAATAAAGTGAAAATCTGTGCAAAAACATTTACATATACTTGCCTACACGTAAGGTATGTTATTACGTGTTATTATATTTTTTATATTTGGATGACCTTTTAGTCTCAAGTGTAAAATTGCACCATGTTTAGAGATAATTGACAGTGAATTGCTGCTTCTAGAGTTAAATGTATTGGATTTCTGTTATAGTCCATCTGCTTTGAAGTGACCATAATCACATTTTGTATATTGAACTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31295
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 |
---|---|---|---|---|---|
ENSDART00000113849 | Essential Splice Site | 131 | 968 | 4 | 26 |
ENSDART00000138947 | Essential Splice Site | 131 | 850 | 4 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 43789698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43875199 |
GRCz11 | 2 | 43728197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTAACTACATTTACTCTATGGATGAAAACCTGGAGTTTCACATTAAAG[T/A]GAGTCTGAGTCTTATTCACTCTTTCTTCCTATTCATGGATGGTTTGTTAT
Long Flanking Sequence:
AATCAAATTAAGTTCAGCGGTCCCTGAAAAAAACCCACTTTCAACACTTTATTAAGCAGAACAGCCATTTTCACTTATAATAATATAATAATAAGAACAAAAAAAAACTGTTTTTAAACATCGTAATACATAACATTGCTGAATATTCAGCTTTGCATTACAGAAAATAAATATATATGGAAATAGTAAACTATTTAAGTTTGCAATAATATTTAAATGGCTTTCTAATCTGCTAAAATACACACACACACACACACACACACACACACACACACACACACACACACAAAGAAACTTTTAAACTGCAGCATTTACTAATCAAAATAAAGGCTCAAAATGTAGTTAAATAGTTAGTTTCTTTTCACTTTTCTGACTTTTCGTGGTTATTTTTTAGGGAAATCTCCATGATACAGATGGTATGGGAATTATTCCCAGAATAGTGCAAGACATCTTTAACTACATTTACTCTATGGATGAAAACCTGGAGTTTCACATTAAAG[T/A]GAGTCTGAGTCTTATTCACTCTTTCTTCCTATTCATGGATGGTTTGTTATTTCATTGTCACTTCAGACTTTAAACAATTGTGCATCTGTTATATTGAGGGTGTGTTTTACCTTGGCAGGTGTCATATTTTGAAATTTATCTGGATAAGATTCGGGATTTGTTGGATGGTGAGTGTGGTCGATGTTTTAATGCACATTCACACCAAGAACTGCAATAAAATTAAAAAATGAATGCCCACCCAAGCATGATAATGTTCGATAATGTAAATAATTAAATGCTCAAGCTCTTAAGCAGAATGTGTTCTTATTGGCTGTACATGTTATCATTCATCCGCTTTGAAAATTGTTTCTGAAAGTGATTTCATTTATTTTCTTATTCAATATTCTAACAGTATTACAACAGTTAAGTTTGCATAGCTATAGCCATCCTTTGTATGAATGGACCTTTGAAACTCACATCAGCACTTGATCTAATCATCAATAAGATGCTTTGAAGTGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1774
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000113849 | Nonsense | 138 | 968 | 5 | 26 |
ENSDART00000138947 | Nonsense | 138 | 850 | 5 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 43789559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43875060 |
GRCz11 | 2 | 43728058 |
KASP Assay ID:
554-1767.1 (used for ordering genotyping assays)
KASP Sequence:
TTATATTGAGGGTGTGTTTTACCTTGGCAGGTGTCATATTTTGAAATTTA[T/A]CTGGATAAGATTCGGGATTTGTTGGATGGTGAGTGTGGTCGATGTTTTAA
Long Flanking Sequence:
TGAATATTCAGCTTTGCATTACAGAAAATAAATATATATGGAAATAGTAAACTATTTAAGTTTGCAATAATATTTAAATGGCTTTCTAATCTGCTAAAATACACACACACACACACACACACACACACACACACACACACACACACACAAAGAAACTTTTAAACTGCAGCATTTACTAATCAAAATAAAGGCTCAAAATGTAGTTAAATAGTTAGTTTCTTTTCACTTTTCTGACTTTTCGTGGTTATTTTTTAGGGAAATCTCCATGATACAGATGGTATGGGAATTATTCCCAGAATAGTGCAAGACATCTTTAACTACATTTACTCTATGGATGAAAACCTGGAGTTTCACATTAAAGTGAGTCTGAGTCTTATTCACTCTTTCTTCCTATTCATGGATGGTTTGTTATTTCATTGTCACTTCAGACTTTAAACAATTGTGCATCTGTTATATTGAGGGTGTGTTTTACCTTGGCAGGTGTCATATTTTGAAATTTA[T/A]CTGGATAAGATTCGGGATTTGTTGGATGGTGAGTGTGGTCGATGTTTTAATGCACATTCACACCAAGAACTGCAATAAAATTAAAAAATGAATGCCCACCCAAGCATGATAATGTTCGATAATGTAAATAATTAAATGCTCAAGCTCTTAAGCAGAATGTGTTCTTATTGGCTGTACATGTTATCATTCATCCGCTTTGAAAATTGTTTCTGAAAGTGATTTCATTTATTTTCTTATTCAATATTCTAACAGTATTACAACAGTTAAGTTTGCATAGCTATAGCCATCCTTTGTATGAATGGACCTTTGAAACTCACATCAGCACTTGATCTAATCATCAATAAGATGCTTTGAAGTGGATTGTCAAAAGGTTGTAGAAATATGAAGCTGCTTTTCTTATAACAGAATTTTCTCTCCTTCTCTTACAGTTTCAAAGACTAATTTATCTGTACACGAAGATAAAAACAGGGTTCCTTATGTCAAGGTGAGTTTCTCAAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39921
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113849 | Nonsense | 673 | 968 | 17 | 26 |
ENSDART00000138947 | Nonsense | 673 | 850 | 17 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 43775775)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43861276 |
GRCz11 | 2 | 43714274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTAGAGCAGAAGAAGAGACAGCTGGAGGAGGATGTGGACTCTCTCAAT[G/T]AAGAGCTGGTCAAAATCAGCGCTCAGGGTATTTATACACTCAGATGCATG
Long Flanking Sequence:
AATAGCTTAATATTTAGCACATTGTTTAGCTATAATTAAACATTTGTTAATATTTGGACTAAGCCAACGTTAAACCATCATATCAACAGTACTAAGGAATGTCATTTTTCTGCAGCAGCATGAAGGCAGTGGTCTTATAGACGAAGAGTTCACTGTAGCCAGACTCTACATCAGCAAGATGAAGTCCGAAGTCAAATCAATGGTCAAACGTTGCAAACAGCTGGAAAACACTCAATCTGAGAGTAACAAAAAGATGGATGAAAGTGATAAGGAGCTTGCAGCATGCCAGTTACGCATCTCCCAGGTAAGACTTCACACTTTTGTGCATGTTAAAGATGTTATTCCTAAAGCTATTGCATTATAAACACTTTAAAAGTATTGATATTAACAAGTGGGTGTTTATTTTGCAGCATGAAGCGAAAATCAAATCTCTGACTGAGTACCTGCAGAATGTAGAGCAGAAGAAGAGACAGCTGGAGGAGGATGTGGACTCTCTCAAT[G/T]AAGAGCTGGTCAAAATCAGCGCTCAGGGTATTTATACACTCAGATGCATGCATGCTAAGTTTTATTTTCTGTGTTTGTGATGTTTTGTGTGCGTGTTTGTGGCCACAGAGAAAGTACATGCGATGGAGAAAGAGAGTGAGATTCAGAGTGCCAATGAGGTGAAGGTAAGAAACATGCATACACAAGGCTTGTTCAGTTTGCACATTTATTTTTATTTCAATGTGAACGGTTGTTTGTTTGTGTGTGTAGGAGGCAGTTGAGAAGCAGATCCAGAGTCACAGGGAGGCTCATCAGAAACAGATCAGCAGCCTGAGAGATGAGCTGGAAACCAAAGAGAAACTCATCACTGATCTGCAAGAGTACGATACACACATTTCAGTTAAAGCAAAAGCAATTGGACAAACATATAGACTGGCAAACTATAATTAAAACAGCAAAAGGAAATGTCCAGCAGCTAGCAAGCTAATACAAACCTTACAGTATAGTCAAATTTGAGCGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19854
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 |
---|---|---|---|---|---|
ENSDART00000113849 | Nonsense | 965 | 968 | 25 | 26 |
ENSDART00000138947 | None | None | 850 | None | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 43768802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 43854479 |
GRCz11 | 2 | 43707477 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCTACCAGAACAGCCAACCTATGCCTATCAGAGGAGGTGGCACTAAA[C/T]AAGAGAAGAGGTTTGTGCTGTTTTCTTCTTCTTTGAGTCTGCTTATTAGG
Long Flanking Sequence:
GTATTCAAGTGTTGATATTAAAGAATGAATCTTCTCTCTCACACAGCTGGTGCGTGATAATGCCGACCTGCGCTGTGAGCTTCCTAAACTGGAGAAGCGTCTGCGGGCCACAGCCGAGCGAGTGAAGGCTCTGGAGACTGCGCTCAAAGAGGCCAAAGAGAACGCAGCCCGTGACCGCAAGCGCTACCAGCAGGAGGTGGACCGCATCAAAGAGGCCGTCAGAGCCAAAAACATGGCCCGCAGAGGACACTCCGCACAGATAGGTGACTGCACACTTACAGAAATAATGCTGTGACTGTCGGTGGTTTGTTTAGAATTAATTCATGTTCACACATAGGAAATAATGACGAATTCTCTCTTTTTCTTTGATTGTAGCTAAACCAATCAGGCCTGGACAGCAACCTGTAGCTTCTCCTACACACCCCAATGTGCTGCGTGGAGGTGGTGGTGTCCTCTACCAGAACAGCCAACCTATGCCTATCAGAGGAGGTGGCACTAAA[C/T]AAGAGAAGAGGTTTGTGCTGTTTTCTTCTTCTTTGAGTCTGCTTATTAGGGATACACTGAATTTTCAGTTTTTGGGCGAAAGAGAAAAGGGCTTAAAAAAGGCTATGCTGTGTCGCATGCCCCAGCAGTGCTAGTTTCACTCTTTCTGCTGTCGAAGTCACTGCTTGAACTGAAGCAGCTTTCACACAAAAGAGCAGTGGAGCACATCTTTGACTAGTTTGCGTGTGCTGTGGTTTAAGTAAAAAAAAAAAAAGCTTAATATTCCACTTGTGTTACTTTTCTGTTTTTACCTAATTCTTTAGGTAAAAAATATTTAATAAAGAGTGATATATTGTGTGTATATATACAGTTGAACTCAGAATTATGAACCCCCCTTAGAATTTTCTTTTCTTTTTTAAATGTTTTCTAAATGATGTTTAACAGAGCAAGGACATTTTCACAGTTTGTCTGATAATAAGAGAAAAAATTCACATCACAATATTTTTTTTCTGGAGAAAGTA
Associated Phenotype:
Not determined