Busch Lab

ZMP

kif15

Ensembl ID:
ENSDARG00000012073
ZFIN ID:
ZDB-GENE-050622-16
Description:
Wu:fc51g12 protein [Source:UniProtKB/TrEMBL;Acc:A0JPF4]
Human Orthologue:
KIF15
Human Description:
kinesin family member 15 [Source:HGNC Symbol;Acc:17273]
Mouse Orthologue:
Kif15
Mouse Description:
kinesin family member 15 Gene [Source:MGI Symbol;Acc:MGI:1098258]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa45858 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa38135 Nonsense Mutation detected in F1 DNA Not yet available
sa10447 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa45858
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099866 Nonsense 749 1378 18 35
ENSDART00000099868 Nonsense 749 1010 18 25
ENSDART00000130782 Splice Site None 1372 None 34

The following transcripts of ENSDARG00000012073 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 36143704)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34577972
GRCz11 25 35082930
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGCCAAGAACAGAAAACTACTTCAGCAAATGAGCAAGCTGGAAGAA[C/T]AGGTTACCATCGCAACTGAAAAGTCTAATCGCACAGAACAGGTGTGTTTC
Long Flanking Sequence:
GACATTTTTGTAAAAGACATTTTTTAAAAAGCTGCTTAACTAACCTAAATTTGCTAATGTAACTAATATCCTGGCTGAAGCTATGCTCAGTTTGTAAAACCAGGCCTCCATATCATTTTAGACTGTTTATAACATTTAGATATATTATAACAATTTAAGTGTATGTGCGGTTTATCTGCTTTACATGTTTATTTTTTTACAAATTATTTACACTACTATTTAGCAAAAAATAATTGTAAATATCAAAAGGCTTTTTTTAATGCAACCTTTTTTAATCACAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGCGATGAAGGATCTGTTAAAACCCTTTCCTTTTGGTTTGATTGTAGGAACAGGCCCTTCGTGTCCAGGGCCAGTTAGATGAGGAGGAAGCCAAGAACAGAAAACTACTTCAGCAAATGAGCAAGCTGGAAGAA[C/T]AGGTTACCATCGCAACTGAAAAGTCTAATCGCACAGAACAGGTGTGTTTCCATTTGTTCAAAAGAGTGATGTATTGATCAAACCATCTTTTAAAATACCTTACATATTTAAAATATTTATTTGAAATATCTGATATCCCTAATAATATCTTTTTTTGTGTGTTTTGATATCTGTTTGCATGGGCTTATAATGTTAGTTTACCCAAATATTAAAATTAGCCTATGATTTACTCACCCTCAAGGCATCATATGATTTTCTTTCTTCAGTCGCATCAGTCATAATTTTTTTAATAGTTATTTTGAGATTTTCTATCTCCACAATGGCAACAGTTGGCTTTTTTTTAACAGTCCAAAACATCAAAGCACATCCATTCATGATAAATGTGCCTCTCATGGCTCTAAAAGGTGAATAAAGGTCTCCTGTAGCGAATTAGTGCAATCTTAAAAGAAAAATATAGATATTTATTACCTAATCAATCGTTTTTTGTCATTTCTGCTAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38135
Status:
Mutation detected in F1 DNA
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
ENSDART00000099866 Nonsense 895 1378 21 35
ENSDART00000099868 Nonsense 895 1010 21 25
ENSDART00000130782 Nonsense 877 1372 20 34

The following transcripts of ENSDARG00000012073 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 36139954)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34574222
GRCz11 25 35079180
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGAGCTGGATCAGCACACACAGCAGATGGAGCTCAAGAGCAGAGAGTG[T/A]TCACAACTTCAAACCAACATCAACGTCAGTATTCATTCACACACACATGC
Long Flanking Sequence:
TCACTTTTTCAGTAAGCAGAGAGAATGTGTGTCTGATTTCAGCAGGAAACAGCTCTCTTCTGATTCATTTAAAGATTTATTTTACATTGCATTTATGATGATTACATGTTATCATACATTGTAGAGGGTCAATCAAACTCTCATGGGAATTAGATGATCGAACCTAATGGGAAGGCAACCTAAAAATAATTGTTCCAAACTTTTAGCTGCAATTGTTTTGTTTAAAATATATATATAACTTACCCATTGTGAAAGCGATCTAAAATGGGCCGTTTAGGTCAGAGGTATTATAACTGGGTTGTTACAAGTTGCTTATTTTCTGTGTATGATTTTTATTTATTTAATTTAAATGACGTTCAGTTTGCCCGTGTCAGGTTGGAGTGGGAGCAGGTGCTGGAAAAGCAGCGTGTTCTTCAGGACACGTACGACACGCTGCAGGCTGAGTTTCAGTTCGAGCTGGATCAGCACACACAGCAGATGGAGCTCAAGAGCAGAGAGTG[T/A]TCACAACTTCAAACCAACATCAACGTCAGTATTCATTCACACACACATGCTGGTATTGGTGGCTTGCAGACTTTCTATGGGAGTCATTTATACAGTAAAACTGCTTATTATGTGGCCTTACACCTCCACCCCTGGCCCTGAATCCAACAGGAAACCTCTTTGGCAAGTTTTAAATGTGAAAAGACCTTGTTAAGTATAATTAGGCGTTTTTTTAATTTTTTAATTACATGGACACAAGGCATGTGCTCTTAAACCACCTTAATAGAGTGGAAATGGATCATACCCTTGTAAGTATATTAATTTCTGTCCTTGTAAACCACTGAAACCAACACACACACTTTTGTTCTAAAGAGGTTTTCAGATACTGTGCTCACTTGTAACAGAGCTTTACTAGTGGTTAGATATGATTTTAAGGTCTGGTTTCAATGTTTAACGTCATTACGTGATCGATTTAGATGTTTTGAAAGCATTAAAGATTTGGTTTTGCTTGCAGGAGTTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10447
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099866 Nonsense 1034 1378 26 35
ENSDART00000099868 None None 1010 None 25
ENSDART00000130782 Nonsense 1016 1372 25 34

The following transcripts of ENSDARG00000012073 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 36135409)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 34569677
GRCz11 25 35074635
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAKGGYTTTCTGTGCAGGGAAAGTACAGCGCAGTGTGTGCWGAGAAGGAG[C/T]AGATGAAGGAGAGCATCACACGMATGAAAAGTGAACTGCAGGAGCTGCGA
Long Flanking Sequence:
GATTCTGAGAGCATAAAATGCAGTGTGCGTTATTAAAAATGTTCATTTCTTCTCTTTGTAATCATAGAAAAATACATAATTAAGACTAAAACTAGTGCATAACTGAACCCCCTTTCCTGCAAAATACTGCATACTTTTCAAAAAACAGCATATGAATGTTATTTTGCTTGCTTGCTATTGAATACTTCATATAAGACACTAGCATCATAAGCACATAAAATAAATAACTCATGTTTCTGTAGTTTTTTTTTTTCTCTCATGTATGTCACATCTTCATCTGTGTGAATGCAGGCTGTGCTGCTGGAGTTAATGCAGGAGGCCAGAGATCTCCGAAATGACGTGGCCGAGAGAGACCAGACTGTGTGTTCGCTGCGAGCGGAGATCGCCGACATCACCGTGAGTTTCTCTGTTCACTTTCTACACATTCAGAAAGTATATCTTGACATTTTAAATGGTTTTCTGTGCAGGGAAAGTACAGCGCAGTGTGTGCTGAGAAGGAG[C/T]AGATGAAGGAGAGCATCACACGAATGAAAAGTGAACTGCAGGAGCTGCGAGAGGCTTCAGACAGACGTCTCGCTTCTGACCGTGTCGAGGTTTGTGTATTTCTGGGATTGTGTGTGTTTTTAAGATTTTTGTCAAAAGCCTTAACTGAATGATGTGTTTTGCAGCTGGAGCTGCTCCAGGAGGATCTGTCTTACGCCACAGATGAGATGGAGAGACTCGGTAAAGTGGTGGAGGAACAGACAGCCTTGCTAGAGGCTTCAAAGAGCCAGAACACAGAGAAGGAGAACAATATAAACACACTTAAAGAACAGGTACTGCTCATGTCTCCTTCACAATTTAAGGTCTCAAAGGGACAGTTCACGTCTTGACCAAACCTGTCTGAGTCTCTTTAATCAGTTACACACAAAAGAAAATATTCTGAAGAATGCAGAAAAACAAATAATAAACCGTCCTTGACTTCCATAGTATCTTTTGGTCCACTATTGATGTCAATGGTCGCT
Associated Phenotype:
Not determined