ZMP
kif3c
Ensembl ID:
ZFIN ID:
Description:
kinesin family member 3C [Source:RefSeq peptide;Acc:NP_001017849]
Human Orthologue:
KIF3C
Human Description:
kinesin family member 3C [Source:HGNC Symbol;Acc:6321]
Mouse Orthologue:
Kif3c
Mouse Description:
kinesin family member 3C Gene [Source:MGI Symbol;Acc:MGI:107979]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23137 | Nonsense | Available for shipment | Available now |
sa23136 | Nonsense | Available for shipment | Available now |
sa36475 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36474 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23137
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128715 | Nonsense | 74 | 759 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 37381202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 37266099 |
GRCz11 | 17 | 37213684 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAAATCCTCCGGAAGCCTCGTCAAATCATTCACGTTTGATGCCGTCTA[T/A]GACGTAAGCTCAAAACAAAACGAGTTGTACGACTATGCATGCAAACCTCT
Long Flanking Sequence:
TCCACCTATCAGCATCCGTCCGCCCGTGAGCGCGCTCTGCCTATTGTCTGCGGGGAACAGGGCGTGTGCCGCCGGAGAGGGAGATGCGCGAGCCTCGCTGCATGGAGCGGTTTGTGATGCTGGCTTTGGACCACCAAGATGCTCTGCGCACACGTTTACATGGGACGGACGTGCATTTGCCGCATTTATAGCCTTTATGCGAATGAGTGTTTTCTGTCATCGCTCCTCGCGTCCTTATATAAAACAGCAGCATATTAAAGACGCGGATTTTTCATCAAAATGATGAAGAGAAACAGCCTATTGCGACCGCGCTCCATGTCGATTGGCAAGAAATCAGAGGCGGTGAAGGTGGTGGTGCGATGCCGCCCTCTAAACAAGAAGGAAGAGGCGATGAATCAGGAAAGAATTGTTGAAGTGGATGTCAGACTGGGACAGGTGAGCGTGCGTAATCCCAAATCCTCCGGAAGCCTCGTCAAATCATTCACGTTTGATGCCGTCTA[T/A]GACGTAAGCTCAAAACAAAACGAGTTGTACGACTATGCATGCAAACCTCTTATTGACTCTGTTTTGCTCGGGTTCAATGGAACAATATTTGCATATGGGCAAACTGGCACAGGCAAAACATACACAATGGAAGGTGTGCCCACAGACCCCGAGACCAGGGGAGTCATCCCAAACTCGTTTCAGCACATATTTACTCAAATATCCAGGTCTCAGAACCAGCAGTATCTCGTGAGAGTGTCTTACATTGAGATTTATCAAGAAGAGATACGAGATCTCCTCTGCAAGGACAACAACAAAAAACTAGAGCTCAAGGAAAACCCCGAGTTGGGCGTCTATGTTAAAGACCTCTCGTGTGTTGTGACCAAGAACATAAAGGAGATCGAACACGTCATGAACCTGGGGAATCAATCAAGATCTGTCGGATTCACCAAAATGAATGAGCGCAGCTCCAGGTCTCATGCGATTTTTGTCATAACTATTGAGTGCAGTGAAATGGGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23136
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128715 | Nonsense | 159 | 759 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 37380947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 37265844 |
GRCz11 | 17 | 37213429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTCTCAGAACCAGCAGTATCTCGTGAGAGTGTCTTACATTGAGATTTA[T/A]CAAGAAGAGATACGAGATCTCCTCTGCAAGGACAACAACAAAAAACTAGA
Long Flanking Sequence:
TAAAGACGCGGATTTTTCATCAAAATGATGAAGAGAAACAGCCTATTGCGACCGCGCTCCATGTCGATTGGCAAGAAATCAGAGGCGGTGAAGGTGGTGGTGCGATGCCGCCCTCTAAACAAGAAGGAAGAGGCGATGAATCAGGAAAGAATTGTTGAAGTGGATGTCAGACTGGGACAGGTGAGCGTGCGTAATCCCAAATCCTCCGGAAGCCTCGTCAAATCATTCACGTTTGATGCCGTCTATGACGTAAGCTCAAAACAAAACGAGTTGTACGACTATGCATGCAAACCTCTTATTGACTCTGTTTTGCTCGGGTTCAATGGAACAATATTTGCATATGGGCAAACTGGCACAGGCAAAACATACACAATGGAAGGTGTGCCCACAGACCCCGAGACCAGGGGAGTCATCCCAAACTCGTTTCAGCACATATTTACTCAAATATCCAGGTCTCAGAACCAGCAGTATCTCGTGAGAGTGTCTTACATTGAGATTTA[T/A]CAAGAAGAGATACGAGATCTCCTCTGCAAGGACAACAACAAAAAACTAGAGCTCAAGGAAAACCCCGAGTTGGGCGTCTATGTTAAAGACCTCTCGTGTGTTGTGACCAAGAACATAAAGGAGATCGAACACGTCATGAACCTGGGGAATCAATCAAGATCTGTCGGATTCACCAAAATGAATGAGCGCAGCTCCAGGTCTCATGCGATTTTTGTCATAACTATTGAGTGCAGTGAAATGGGCATTGATGGTGAGGACCACATTCGTGTTGGAAAGTTAAACATGGTGGATCTTGCCGGTAGTGAGCGCCAAAGCAAAACAGGTGTGCAGGGACGAAGATTTAAAGAGGCTGCAAAGATCAACTTGTCTCTTTCTGCTCTTGGAAATGTCATTTCGGCTTTGGTGGATGGAAAGAGCACCCACGTCCCCTACCGGGATTCCAAACTCACGCGCTTGCTACAGGACTCACTGGGGGGCAATGCTAAAACCGTTATGGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36475
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128715 | Nonsense | 393 | 759 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 37380247)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 37265144 |
GRCz11 | 17 | 37212729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGGCGCAGCTCGAAGAACGAGGGATGCTGGCGAAAGAAAGAAGACGA[C/T]AGAAGAGAAACAGCCTCAGGATGAAGAGGAGTATGAGTAGCGGAGAGGTG
Long Flanking Sequence:
CTCATGCGATTTTTGTCATAACTATTGAGTGCAGTGAAATGGGCATTGATGGTGAGGACCACATTCGTGTTGGAAAGTTAAACATGGTGGATCTTGCCGGTAGTGAGCGCCAAAGCAAAACAGGTGTGCAGGGACGAAGATTTAAAGAGGCTGCAAAGATCAACTTGTCTCTTTCTGCTCTTGGAAATGTCATTTCGGCTTTGGTGGATGGAAAGAGCACCCACGTCCCCTACCGGGATTCCAAACTCACGCGCTTGCTACAGGACTCACTGGGGGGCAATGCTAAAACCGTTATGGTGGCCACTGTTGGACCAGCTTCATGTTACTATGATGAGACTCTCACCACGCTGAGGTACGCAAACAGAGCGAAGAACATCAAGAACAAGCCAAAGATCAACGAGGACCCCAAAGATGCCCTGCTCCGTGAGTTCCAGGAGGAAATAGCCCGTCTGAAGGCGCAGCTCGAAGAACGAGGGATGCTGGCGAAAGAAAGAAGACGA[C/T]AGAAGAGAAACAGCCTCAGGATGAAGAGGAGTATGAGTAGCGGAGAGGTGGAAACTCCGAGAATCGGAGAGGTAGAGGTTGTTGAGACGGTTCGGGAGGAAAGCGTGGAGGACTATTGGTGGAAGCAGCAGATGGCAAAGACCTCTGCCAATTACAAGCCAGATATTAGCAGGAAACTTGGCATGGTAAACGAGAAAGTAAAGACTGTGGAAGAGTTGCTGAAGGAGCAACAAGCTATGGAAAATATGATCGAAAAATACAAGGTTGGTTCTTTCCACCCAACTTTTTTCTTTGTAGAGATTATACACTATATCATTTATTAATCACATCCTTTACTGCATGCCATGTTTTTCTTTTTTTTTTTTTAGGCTATGGAAAGTAAGCTTCTGGTTGGAGGGAAAAACATCATTGACCACACCAATGAACAGCAGAAAATGCTGGAACTGACGAGGCTGGAGATTGCAGAGCAGGTAACTATCAAAAGTAGTAGGCTTTACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36474
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128715 | Essential Splice Site | 556 | 759 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 37378318)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 37263215 |
GRCz11 | 17 | 37210800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGCTTTTTTCTTTCCCCTCGGTCAACCTTGCTTTGGTTGCTCCTCTCA[G/A]TTTTACAGTAAGCTGCAGTTGGTGAGATCTGAGATTGGAGATATCATCAA
Long Flanking Sequence:
TTGTATATTTAAATAATCTTTAAAAATCATTCAACAACATGTGAACAATGTAAAAATTCTGAAGCCTACTCATAGTCAAAAACATTTTTAAAAATATGTGTTAATAATGCATTAAAACAGTCAGGAAAAAAACGCTGTGTTCAAGGCAGAATTAAAGAGTTTTTCATTCTATACACAAAGGTGACTTTATTGTGTTTTATGTAAATTCAGACCATGAGTCTGCATATATGGACATATTCTTTTCTAAAAGTACATCATATGAAAAGATGATACTTAGGTTTAATTCCAATAAGCCCAAATAGCAAAGAGAAATAAAAAATGCATATAAAAATCAGCTTGAGCCTTAAGAGGTTAACCAGACTGGTCAAATGTGTGTATTTGATGTTTGTATGATGAAACACACACTGTATAAACCACATTTAATACATTATGGCAGCTAAATCATATCTTAGTGCTTTTTTCTTTCCCCTCGGTCAACCTTGCTTTGGTTGCTCCTCTCA[G/A]TTTTACAGTAAGCTGCAGTTGGTGAGATCTGAGATTGGAGATATCATCAATGAACATGTCACAATGAGGCAGGAACTGGAGCAGACGATGAACGAGCTGACAAGAGAGATGAAATTCAAGTACGTCCCACCAGTCCTCGCTGTTTTGAACTATACAAAAACACGTGTGTGCATGAGTTTTGTCTGTTTGTATTTCCGCCAGAAATCTGATCATTGAGAACTTCATTCCTCCGGAGGAAAAGAATAAGATCATAAATCGGCTCCACTTTGATAGCGAGGAAGACCAGTGGAAAGTTTTACCTCTTCTCCCTTCAGAAAAGTATGAACCATTGTTTCAAACACTGCTGGACTAGGATGATTAGAAACTTACGTCATGATGTTGTGTTTGATCTTATTTTCCAGTAACTCACCTCTCGTCCGACGAAGACCAACTTCTGTAGTGGGAAACAAGAGACCAGTTAGTATGTACGCTCAAACTGCCGTGGCACACGGGTCGCCTTC
Associated Phenotype:
Not determined