Busch Lab

ZMP

kif14

Ensembl ID:
ENSDARG00000062187
ZFIN ID:
ZDB-GENE-030131-5759
Description:
kinesin-like protein KIF14 [Source:RefSeq peptide;Acc:NP_001038441]
Human Orthologue:
KIF14
Human Description:
kinesin family member 14 [Source:HGNC Symbol;Acc:19181]
Mouse Orthologue:
Kif14
Mouse Description:
kinesin family member 14 Gene [Source:MGI Symbol;Acc:MGI:1098226]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa43838 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24165 Nonsense Available for shipment Available now
sa31072 Nonsense Mutation detected in F1 DNA Not yet available
sa43839 Nonsense Mutation detected in F1 DNA Not yet available
sa43840 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa43838
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089622 Essential Splice Site 498 1506 8 29
ENSDART00000147825 Essential Splice Site 301 1307 8 29
Genomic Location (Zv9):
Chromosome 22 (position 22807412)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 22419048
GRCz11 22 22444026
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAAGTGAGCGCTGTACTTCAGCCCAGACCAGCGGAGACCGGCTCAGGG[T/C]AATCCAGCATCCAAAAGCTCTGTTTATTCAATCTGAAGATTACTTTGTGC
Long Flanking Sequence:
TGCTTACATTAACCAGAAAACAAACTATTTAAGGGAAAGTTCTCCCAAAATATAAAATTCTGTCATCATTTTCTCACCTTTGAGTTGTTCCAATCACCGTTGTTAGTTAAACTTTTTCTGCTGAACACAAACGGAGATATTTAGGGGAATGTTGAAAACCGGTAGCCTTTGACCTCCATATTAGAAAAAACATATACTATGGAAGTCAATGGCTGCTTCAAAATGTCTTATTTTCTGTACAACAAAAGAAAGATCATCAAAGACCGGTCTGTAACAATTGGACGGTCAGTCAATGATGACAGAAGTGTAATTTTTGCATTGAGCATCGCTTTAAGTGCATTTGTGACTGTTTTACCCACCTAATGTTTCTTCATGTGCACAGACGGAGTTTGTGGAGGAAGAGGAACACGATCACTGCATCACCAGCCGAATAAACCTGGTAGATTTGGCGGGAAGTGAGCGCTGTACTTCAGCCCAGACCAGCGGAGACCGGCTCAGGG[T/C]AATCCAGCATCCAAAAGCTCTGTTTATTCAATCTGAAGATTACTTTGTGCTGCTTTCTCTTGTATACATGGGTGACGTATACGTATATTTGTTTTATTTAGTGTTTATATAAATTGGGGCTGCACAAACTTATAGAATATAGGCTACTCTACCTATCCTAAAAAAAGACTTTCTTTAAAAATTGTAAAGTCTGTGTGAACCAGTAGTTGTTGAGACTTTTATTTCAACATGTTGATGTGCTTCCCACTGGAGTGAAATATTGAGGTGGGGGCAGGGCTTTCATTTTGCACATCATTCCCTCATAGTAAACTTGCTGTAGGAAGAGCAAGATTAAGAACACTGGGGTTGAAGCTGTCAAACTGACATCAGAGAAGAATCACAACTCCAAACGCGAAAGCAGATGATCAGACTTTGAAGATTAACAAAACAAAATAAAAAATATTCACTGGATTAACTTGCACGGATTAATTGTTCACCTAAAGACTAACAATGTCCTCTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24165
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
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089622 Nonsense 624 1506 11 29
ENSDART00000147825 Nonsense 427 1307 11 29
Genomic Location (Zv9):
Chromosome 22 (position 22811152)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 22422788
GRCz11 22 22447766
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGATGAGCTCTCAGGGAGTCGAGCCGGAGAAGATGAGACTCTTTCAG[C/T]AAGAGATTGCAGCGCTCAAGAACAAACTCTGCCAACAGGAGCATGAAATG
Long Flanking Sequence:
AGTCATTGAGTAGAAACACTGCAGCACACCACAGCTCCACTAGAGGGCAGTACATAAGTGACTACTATCACTTGCGCTGATCTGTAGTCAGTACAGAAATTAAAACAGAAATTAAAATGGAAAAGGTTTATGTTGATGGTAGTTGTTGTTATTGATAATACTGATAAAAAATTATGTTTTTTAGTTTTTATATTATCATTAATATTATAAATAATACAAACAATTGTTATTTTTTTATTTGAATTGTCTTTGTTGTTTAATATTATTTATGAATTATGTATAATAATAATACATTTTCACTGATAATACCATTTATTAGTCATTTATAATGCATTATAGTTTCATTTTGATATTAATTCTTTTCTAAGATGTTTTTGTTGTGTGAGATTCGAGTGTTTTCTAAATCTGTGTGTGCAGATCTGAAGGCTGAGGTGGAGAAGCTGCGAGCAGCTCAGATGAGCTCTCAGGGAGTCGAGCCGGAGAAGATGAGACTCTTTCAG[C/T]AAGAGATTGCAGCGCTCAAGAACAAACTCTGCCAACAGGAGCATGAAATGGCTGAAGCTCACAGGTGTGTTCATATAAAACAAAGAAATCAGGGTTATTAACCACATTATGCAATCAAAATTTTAAAACTGGTACATCAAAATTACCTGTCCAAAACTTACCTCATATAAAAATGTAGTTTTTCTAAAGCATTCCGTTTAAATATGCAACTGATGAATTATTTCATTAAAGGGTTAGTCCACTACTATATTATATTTTAAACTTTAGGTCATGTGTAATGTAGCTGTGTGAACATAAAACATCATCTCTGAATGTAATACACTCAAAGTTCAATGCAAAGGGAGACATTGGCTTTTACAGAGCTAGCTTAGCAAAGCCTACAGGGAACGAATTTGGGGACTACAAAAAATAAATCCGAGTTAATGAAATCATAAACCCTGCAGGTTACGTGCATTCACCACACGCCTTTAAGTTCTTGTAAGTGTTTTTATTTGATAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31072
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089622 Nonsense 700 1506 13 29
ENSDART00000147825 Nonsense 503 1307 13 29
ENSDART00000089622 Nonsense 700 1506 13 29
ENSDART00000147825 Nonsense 503 1307 13 29
Genomic Location (Zv9):
Chromosome 22 (position 22816532)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 22428168
GRCz11 22 22453146
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGAATGAGGATCCGCAGCTGTCAGAGATGCTGCTGTACATGATTAAA[G/T]AGGGCCAAACCAAGGTCGGCAAGCTCAAGTCTGAGTCGGCACACGACATC
Long Flanking Sequence:
TAATTAAAATTATGATAATAATAAAAATATCAATAATGATAATGCTAATAAAGAATAATAAATAAATAAATAAATAAATAAATAAATAAATAATATGATATATTTAATATTGTTGTAATTATTATTGTATTTTTTTTGGATATTGGATTTCGTGATTAATATTATACAACATTGCAAACATTTCTAGATGATTATATGTTTCTAATTATTTCCCATGTTATTGTGTCCAGAACATGGAAGGAAAAACTAGAAGAGGCTGAGAGGAGGAAACGAGAGGAAGCCAAAGAGCTTCAGGTAAATCTTCGACCCTTTACTTTGTGTGTGATGGATCGATGAGCTTTTCAAATGAGTTTCATGGCCATTTTCTGTCTCTTTCTGCTTCTTCTCTGTGTGTCGTTTAGCGTGCCGGCGTCACCTTTAAAGTGGATAATCGGCTGCCTAACCTTGTGAACCTGAATGAGGATCCGCAGCTGTCAGAGATGCTGCTGTACATGATTAAA[G/T]AGGGCCAAACCAAGGTCGGCAAGCTCAAGTCTGAGTCGGCACACGACATCCAGCTGTCTGGAGCACTCATCGCCGATCAGCACTGGTGAGAACTGACGCGCCTCATTTTTTGGTTAAAATTCACCTTTTTATTAACAGGTCAGTTATAAGATTTGTATAGGTCTGATGAAAAATAATAAAATAATAAATTATTTTAATAAATTTGTTTGTGTGTGTATTTAATTTATATATTTATTTATTTAATTTATATGTTTGTAAATTTTTACAATTTCGTTTTGTTAATTTTAACCATTTATTTTTGTTATGTTTGTATATTTAAATATTTTCAAAATTTTTATGCATTTTTAACTTTGATTTATTAAAATGATTAAATCGATTTATAATTAATTTTAATAAGGTATTTTGTTATTGTTTTATTTAAAAATAGTTTTTTAGATTTTCTTTTTAGTTATTTTTTCATGTTTATTTAAATATTGATTTATTTATCTATGTGTTTGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43839
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089622 Nonsense 700 1506 13 29
ENSDART00000147825 Nonsense 503 1307 13 29
ENSDART00000089622 Nonsense 700 1506 13 29
ENSDART00000147825 Nonsense 503 1307 13 29
Genomic Location (Zv9):
Chromosome 22 (position 22816532)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 22428168
GRCz11 22 22453146
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGAATGAGGATCCGCAGCTGTCAGAGATGCTGCTGTACATGATTAAA[G/T]AGGGCCAAACCAAGGTCGGCAAGCTCAAGTCTGAGTCGGCACACGACATC
Long Flanking Sequence:
TAATTAAAATTATGATAATAATAAAAATATCAATAATGATAATGCTAATAAAGAATAATAAATAAATAAATAAATAAATAAATAAATAAATAATATGATATATTTAATATTGTTGTAATTATTATTGTATTTTTTTTGGATATTGGATTTCGTGATTAATATTATACAACATTGCAAACATTTCTAGATGATTATATGTTTCTAATTATTTCCCATGTTATTGTGTCCAGAACATGGAAGGAAAAACTAGAAGAGGCTGAGAGGAGGAAACGAGAGGAAGCCAAAGAGCTTCAGGTAAATCTTCGACCCTTTACTTTGTGTGTGATGGATCGATGAGCTTTTCAAATGAGTTTCATGGCCATTTTCTGTCTCTTTCTGCTTCTTCTCTGTGTGTCGTTTAGCGTGCCGGCGTCACCTTTAAAGTGGATAATCGGCTGCCTAACCTTGTGAACCTGAATGAGGATCCGCAGCTGTCAGAGATGCTGCTGTACATGATTAAA[G/T]AGGGCCAAACCAAGGTCGGCAAGCTCAAGTCTGAGTCGGCACACGACATCCAGCTGTCTGGAGCACTCATCGCCGATCAGCACTGGTGAGAACTGACGCGCCTCATTTTTTGGTTAAAATTCACCTTTTTATTAACAGGTCAGTTATAAGATTTGTATAGGTCTGATGAAAAATAATAAAATAATAAATTATTTTAATAAATTTGTTTGTGTGTGTATTTAATTTATATATTTATTTATTTAATTTATATGTTTGTAAATTTTTACAATTTCGTTTTGTTAATTTTAACCATTTATTTTTGTTATGTTTGTATATTTAAATATTTTCAAAATTTTTATGCATTTTTAACTTTGATTTATTAAAATGATTAAATCGATTTATAATTAATTTTAATAAGGTATTTTGTTATTGTTTTATTTAAAAATAGTTTTTTAGATTTTCTTTTTAGTTATTTTTTCATGTTTATTTAAATATTGATTTATTTATCTATGTGTTTGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43840
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089622 Nonsense 933 1506 18 29
ENSDART00000147825 Nonsense 736 1307 18 29
Genomic Location (Zv9):
Chromosome 22 (position 22822980)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 22434616
GRCz11 22 22459594
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGATCATGATGTCCGGCATGCTAAAATTGTAGCAGCTCTTGAGGCC[G/T]AAAAGAGGAAGATTGCCGAAGATTTGGCTCAGATTGAAATGAAACGTGCT
Long Flanking Sequence:
ACAGCGTTTAGCATTTGTCTGTACTCCAGTTCCTCAAACACCGATGCTTTCTTCTTCAGAAGGAGGAGAGTGAAAGGAAAAGAGAACAGGAGCTGCATAAACAGAGAGCCGCCAGTCAGATTGAGCAGCTGCAGTCTGTAAAAACTCTACTGGAGAAGGAAGTCAGCAGCCATAAGAGACGTCTGCAGATGGAGGCTCAGGCCACTAGACAGGTGAAGAGCTTACTTAATATCTTAATTCATCTCTAGACGTTTTATAAGTGCAAAGGAAAATATATTTCTCTCTCCAAACAAACACCTGTATATAAGTTAAACAAGAACTCTCCATAGGTGTCATATATTTCATAAGTTAAAGAAACAGTCAAAACACTTAATTTTGCTCTTGAATTAATATGAGATTGGTTGTGCTTTTTATTACATTTTTTATCATTATTTCTTTTTTTGTAGGCGATGGCTGATCATGATGTCCGGCATGCTAAAATTGTAGCAGCTCTTGAGGCC[G/T]AAAAGAGGAAGATTGCCGAAGATTTGGCTCAGATTGAAATGAAACGTGCTCTCAAAGTCACTCAAACCCCTAAAATGGGTACTTGCACATATTCCATTTAAAAGACATTGAGTTTTCCATCAGTGTGATGTTCACCATCATCTTCTTCAATATTTGTAGCTATTCCGCAATGGGACGCCATGAAGCTGTCTTTGATGATTGAAGAAGCAAACAAAATCAGCGGCAAACTCAGAAAACACACAGTCTTCAGCAGGTACAGTTATTTAGTGTGTGAGGACATCAATATTTTTGGTTAATAGCATAAAAAATCAGTTTATTTAGATTATCGATAATTAAAATTCAGCTATTTACATTATGGACTTTAAAGAGTTTGTATGTGTTTGTGATTTGACGACAGACACGAGGCTGCTGATAAAGAGGTGGAGGGTGGAGACGCTCAACTGCAGGTCCAGGTTCAGAACACCAAACTGGGCATTTCCACCTTCTGGAGTCTGGAGAAG
Associated Phenotype:
Not determined