ZMP
KIFC2
Ensembl ID:
Description:
kinesin family member C2 [Source:HGNC Symbol;Acc:29530]
Human Orthologue:
KIFC2
Human Description:
kinesin family member C2 [Source:HGNC Symbol;Acc:29530]
Mouse Orthologue:
Kifc2
Mouse Description:
kinesin family member C2 Gene [Source:MGI Symbol;Acc:MGI:109187]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2867 | Essential Splice Site | F2 line generated | Not yet available |
sa5620 | Essential Splice Site | F2 line generated | Not yet available |
sa36082 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10867 | Nonsense | Available for shipment | Available now |
sa36081 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2867
Status:
F2 line generated
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059841 | Essential Splice Site | 20 | 558 | 2 | 13 |
ENSDART00000059841 | Essential Splice Site | 20 | 558 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 16 (position 18619025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16661601 |
GRCz11 | 16 | 16569578 |
KASP Assay ID:
554-3142.1 (used for ordering genotyping assays)
KASP Sequence:
TGGACGAGGGCAGAARATATCAGGAGACGAGAGGAGAGAGTGAGAGAGCT[G/C]CAGCTGCAACTGGACAAAGAACGCAACAAGGAGCCTGTGGTTAAAGTAAG
Long Flanking Sequence:
TGTATCATACATTTTAAACAACAAAACATTTAATGACTATTAATAATTGTTTATTGAAACTGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAATACACTTGCCATGTTATGAGAGCTGAGCTGCTTTGATTTTCTCAAACATATCAAGATAAGTGCAAAGGTCTCTCTCTTTCATACTATTCTCCATATAGAAGGCAGAGACTGAGCTTATTTTGGCACAAGTTGCCTCATTTATTGTACAGAAACTCGCATTCTTCATCTCTTAAAACGTGTGTGAACATCGTGTGTCGTCCCAGATGTTAATAGACCAAATTATGACTTTCCTACTGCCCCTTGTAGGAAAATGAGAACCTGCGCAGTCGTGTTCTGCAGCTAGAGAGTTCACTACAGCAGCGGGCAGAGCAGATGTCCCGTCTGGAGCACCAGAGAGAGCAGAGCGAGTGGACGAGGGCAGAAGATATCAGGAGACGAGAGGAGAGAGTGAGAGAGCT[G/C]CAGCTGCAACTGGACAAAGAACGCAACAAGGAGCCTGTGGTTAAAGTAAGAAAAATGCAACTCAAAAATGTTTTACATTCTCTCAAAAGATTCAAGATTCTTTATTGTCACTGTACTATGTACTGAGTACTTAGCACAGCGAAATAAAGGAAAAAGAATAAAATGCTGGAAGGGCATCTGTTGCATAAAATATATGCTGTATAAGTTGGCGGTTCATTCCGCTGTGGTGACCCCTGATTAATAAAGGAATTAAGCTGAAAAAGAAAATGAATGAAAGAATAAATTAATATAATATGAAGCTCAGCGAAATGTTAACATGAATTAACCACAAAAGAATTTAAACATAAATAATGTGGAGAACTCATAAATATAAACAACAGATCTGTGAATAGTATAAAAAAAATCTCAAAATTTAAAAGTGTAGTAATGTTAACCCTGAGTATGTGGCGGAGCATAAACATGATATTAGTCCTTCAGTAATTTGTATATCTTTTGTCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5620
Status:
F2 line generated
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059841 | Essential Splice Site | 20 | 558 | 2 | 13 |
ENSDART00000059841 | Essential Splice Site | 20 | 558 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 16 (position 18619025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16661601 |
GRCz11 | 16 | 16569578 |
KASP Assay ID:
554-3142.1 (used for ordering genotyping assays)
KASP Sequence:
TGGACGAGGGCAGAARATATCAGGAGACGAGAGGAGAGAGTGAGAGAGCT[G/C]CAGCTGCAACTGGACAAAGAACGCAACAAGGAGCCTGTGGTTAAAGTAAG
Long Flanking Sequence:
TGTATCATACATTTTAAACAACAAAACATTTAATGACTATTAATAATTGTTTATTGAAACTGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAATACACTTGCCATGTTATGAGAGCTGAGCTGCTTTGATTTTCTCAAACATATCAAGATAAGTGCAAAGGTCTCTCTCTTTCATACTATTCTCCATATAGAAGGCAGAGACTGAGCTTATTTTGGCACAAGTTGCCTCATTTATTGTACAGAAACTCGCATTCTTCATCTCTTAAAACGTGTGTGAACATCGTGTGTCGTCCCAGATGTTAATAGACCAAATTATGACTTTCCTACTGCCCCTTGTAGGAAAATGAGAACCTGCGCAGTCGTGTTCTGCAGCTAGAGAGTTCACTACAGCAGCGGGCAGAGCAGATGTCCCGTCTGGAGCACCAGAGAGAGCAGAGCGAGTGGACGAGGGCAGAAGATATCAGGAGACGAGAGGAGAGAGTGAGAGAGCT[G/C]CAGCTGCAACTGGACAAAGAACGCAACAAGGAGCCTGTGGTTAAAGTAAGAAAAATGCAACTCAAAAATGTTTTACATTCTCTCAAAAGATTCAAGATTCTTTATTGTCACTGTACTATGTACTGAGTACTTAGCACAGCGAAATAAAGGAAAAAGAATAAAATGCTGGAAGGGCATCTGTTGCATAAAATATATGCTGTATAAGTTGGCGGTTCATTCCGCTGTGGTGACCCCTGATTAATAAAGGAATTAAGCTGAAAAAGAAAATGAATGAAAGAATAAATTAATATAATATGAAGCTCAGCGAAATGTTAACATGAATTAACCACAAAAGAATTTAAACATAAATAATGTGGAGAACTCATAAATATAAACAACAGATCTGTGAATAGTATAAAAAAAATCTCAAAATTTAAAAGTGTAGTAATGTTAACCCTGAGTATGTGGCGGAGCATAAACATGATATTAGTCCTTCAGTAATTTGTATATCTTTTGTCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36082
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 |
---|---|---|---|---|---|
ENSDART00000059841 | Nonsense | 420 | 558 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 16 (position 18609993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16652570 |
GRCz11 | 16 | 16560547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGGCCATAGCTCGAAAGAACAGGATTACATTTGGAACACAAATGAAC[C/T]AGCACAGCTCTCGATCACATGCCTTGCTCACGGTGACTGTGCTGGGTACA
Long Flanking Sequence:
AGTTAAGATACAACCAGCTCTTATATTCTAACTGCTTGTAATTTTCTAGTGAGCAAAAAGATCACAATTAGCTGGTTCAGGTGTTATTGATGACACCCTTGCTTTAAAAGATGAATGAACGTCTCATGAAAGTCTTGAAACAACATGAGAGAGAGTGAACAATACTGATTGTTTTCATTTTTGAGTACATTGTTGTCTCACATCTATTGTTATATGAGTTATATACTTGTGGTTGCTTGCATCAGAGATCTACTTAGTAAGGATGGGGAGAAGCTTGACATCAAGATCAACCCTGATGGGACGGGTCAGCTCCATGTTCCAGGACTCAGGGTCTTAGAGGTCAAAAACTTCCAGCATATCAAAAAAGTGAGTCCCAAGGTGACATCGTTCCAGAAACAGCTGACTGAATAAAATCCATTCTCTCCAATCATGTTTGTTCTTTCTTTCAGATTTTGGCCATAGCTCGAAAGAACAGGATTACATTTGGAACACAAATGAAC[C/T]AGCACAGCTCTCGATCACATGCCTTGCTCACGGTGACTGTGCTGGGTACAGACCTCGCCAGTGGTGCAAAAACCACCGGTCAGTCCCAATGATTCTTGATATTTAGGATGCATAAAGCCCAGCTGAAATAAAGCGATTTGAAATAATCCTATATGATTGTAGCTTGTCAGGCTGTACAAACATGATTCTCGTGTCAGACTGTAATGTCCTACTGAACAATAATTAATGCATAGACAACACAGACATGAAAGAAAACTCATCTGGAGTTTGACATCATCCATCCATGACATGTGAACAGTGTTGATGAATATGTCAAACCAATGAAGTAAACCAAAGAGTACAGATTTTAGCCAAGGATTAGAGGAATCGTTTAAGATTTTTAGGAATTTGTCTCCGGTGTCACCTCACAGCAACAAGGTCACTGATTCAAATCTCCAACTGGGCCAAGTGTCATTACTGTTCTCATGTTTGCGTAGGTTTCTTTCGGGTGCTCTAGTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10867
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059841 | Nonsense | 461 | 558 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 16 (position 18609076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16651653 |
GRCz11 | 16 | 16559630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCAGGSAAGCTGAATCTGGTRGAYCTGGCTGGTTCTGAGAGGGTGTGG[A/T]AGTCTGGAGCAGAGGGGGAGAGACTGAAGGAAGCCCAGAATATTAATCRC
Long Flanking Sequence:
GGTCACTGATTCAAATCTCCAACTGGGCCAAGTGTCATTACTGTTCTCATGTTTGCGTAGGTTTCTTTCGGGTGCTCTAGTTTCCCTCAAAGCCCAAAGACATGCAGTATGGGTGAACTGGATAAACTAAATTGACCCTATTGTATAAGTGTGTGATTGAGAGTGTGTGGGTAATTCCCAGCACTGAAGTTCACAAGTTAAGATACTCTCAGTGCTGGGTTGCGGCTGGAAGGGTGTTTATTGTGTGGAACATATGCCAAATAGTTGGTGGTTGATTCCCCTGTGGCGAGCCTTAATAGATTAGGGACTAGGTCAAAGGAATGAGAGTGAGGAATTTGTGTTAGATGACCAAATCTTGCCTAAAATCGCAGTGTCTGCTGGGCAAATTCAAGACTTAATGACTAAATAAAAAACGAATAAAAAACTTAATGACAATTCTTGACTTCTTCTCTGCAGGCAAGCTGAATCTGGTAGACCTGGCTGGTTCTGAGAGGGTGTGG[A/T]AGTCTGGAGCAGAGGGGGAGAGACTGAAGGAAGCCCAGAATATTAATCGCTCACTGCTGGCTCTAGGTGATGTGATCCAGGCCCTGAAGGCCCACCAGACTCACATACCATTCAGGAACTCACGACTCACCTACCTGCTACAGGACTCGCTGGGAAAAGGCAACAAAACTGCCATGGTTGTTCAGGTAACAAAGATTTACCAAGACTTAGCTAACACTGTTGTGCTAACCCCATTTCATAATGACACATGTGAAATGCTGCCCATGGTTTGAGCCAAGGTACATTTGATCAGAATATACTCACAGTAAAGCCCATTGCACACTGAATCCAAAATCTTTGCATGTTAAAAAATAATGTCAACCTTGATCACATTTACACACTGCTTTCAAAATCTGATTGAGTTAGATTTCTTTGTTTTGTTAAAATTTTCACGTGCAAAAAAATGCATTTTGAGGGGTGTTTTGACAGTTTACAGCCACCATACAACCAAATCCCAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36081
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059841 | Nonsense | 468 | 558 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 16 (position 18609055)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16651632 |
GRCz11 | 16 | 16559609 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGACCTGGCTGGTTCTGAGAGGGTGTGGAAGTCTGGAGCAGAGGGGGAG[A/T]GACTGAAGGAAGCCCAGAATATTAATCGCTCACTGCTGGCTCTAGGTGAT
Long Flanking Sequence:
ACTGGGCCAAGTGTCATTACTGTTCTCATGTTTGCGTAGGTTTCTTTCGGGTGCTCTAGTTTCCCTCAAAGCCCAAAGACATGCAGTATGGGTGAACTGGATAAACTAAATTGACCCTATTGTATAAGTGTGTGATTGAGAGTGTGTGGGTAATTCCCAGCACTGAAGTTCACAAGTTAAGATACTCTCAGTGCTGGGTTGCGGCTGGAAGGGTGTTTATTGTGTGGAACATATGCCAAATAGTTGGTGGTTGATTCCCCTGTGGCGAGCCTTAATAGATTAGGGACTAGGTCAAAGGAATGAGAGTGAGGAATTTGTGTTAGATGACCAAATCTTGCCTAAAATCGCAGTGTCTGCTGGGCAAATTCAAGACTTAATGACTAAATAAAAAACGAATAAAAAACTTAATGACAATTCTTGACTTCTTCTCTGCAGGCAAGCTGAATCTGGTAGACCTGGCTGGTTCTGAGAGGGTGTGGAAGTCTGGAGCAGAGGGGGAG[A/T]GACTGAAGGAAGCCCAGAATATTAATCGCTCACTGCTGGCTCTAGGTGATGTGATCCAGGCCCTGAAGGCCCACCAGACTCACATACCATTCAGGAACTCACGACTCACCTACCTGCTACAGGACTCGCTGGGAAAAGGCAACAAAACTGCCATGGTTGTTCAGGTAACAAAGATTTACCAAGACTTAGCTAACACTGTTGTGCTAACCCCATTTCATAATGACACATGTGAAATGCTGCCCATGGTTTGAGCCAAGGTACATTTGATCAGAATATACTCACAGTAAAGCCCATTGCACACTGAATCCAAAATCTTTGCATGTTAAAAAATAATGTCAACCTTGATCACATTTACACACTGCTTTCAAAATCTGATTGAGTTAGATTTCTTTGTTTTGTTAAAATTTTCACGTGCAAAAAAATGCATTTTGAGGGGTGTTTTGACAGTTTACAGCCACCATACAACCAAATCCCAAAAAATCTAATTCTGTCACCTGGAG
Associated Phenotype:
Not determined