ZMP
kif5c
Ensembl ID:
ZFIN ID:
Description:
kinesin heavy chain isoform 5C [Source:RefSeq peptide;Acc:NP_001116747]
Human Orthologue:
KIF5C
Human Description:
kinesin family member 5C [Source:HGNC Symbol;Acc:6325]
Mouse Orthologue:
Kif5c
Mouse Description:
kinesin family member 5C Gene [Source:MGI Symbol;Acc:MGI:1098269]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34632 | Nonsense | Available for shipment | Available now |
sa21480 | Nonsense | Available for shipment | Available now |
sa8541 | Nonsense | Available for shipment | Available now |
sa9450 | Nonsense | Available for shipment | Available now |
sa5538 | Nonsense | F2 line generated | Not yet available |
sa38739 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34632
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083567 | Nonsense | 199 | 985 | 8 | 25 |
Genomic Location (Zv9):
Chromosome 9 (position 24236702)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23392488 |
GRCz11 | 9 | 23203357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCATCTTGACTTGTTCTCTGATGTTACATTGTGTTACAGACATGAAT[G/T]AGCACAGCTCCCGCAGTCACAGCATTTTCCTCATTAATATTAAGCAGGAA
Long Flanking Sequence:
TATTTTGAAATATACCTGGACAAAATCAGAGACTTGCTTGATGGTGAGATAAAAAACAAAAAAAAACTATCACTTTTCTCATGAATGTTAAGTTTCTGTTAAAAATTCTATAAATCTGTTTTCATGCACCAAATTTCTTTTTGTTTCCCAATTCTAAAGTTTCAAAAACCAACCTGGCTGTACACGAGGATAAGAACAGGGTGCCCTTTGTCAAGGTAGGACAGATGCACAGCACATAGTTTTCCAATTACAGACGTTATGCAGACAGTGTGTTTTAATGCTCTTCTGTTTGCAGGGTTGCACAGAGCGCTTTGTGTCCAGTCCAGAGGATGTCATGGATGTGATTGACGAGGGTAAAGCCAATCGCCATGTGGCTGTCACAAGTGAGTGACCATTCCCTGATAAAATACTGTACATCTATCCAGAATCAGATATAGCTAATATACAGTGCTGTCATCTTGACTTGTTCTCTGATGTTACATTGTGTTACAGACATGAAT[G/T]AGCACAGCTCCCGCAGTCACAGCATTTTCCTCATTAATATTAAGCAGGAAAATGTGGAGACAGAGAAGAAACTGAGTGGAAAACTCTACCTGGTGGATCTGGCTGGAAGTGAAAAGGCATGTTTCCTCAGCTTTCTGTTTATGTTCAGTTAATTCACTTTAAAGGCAATGATAGGCACCTAGTCATTGGCATTAAAGTGAAATTACTAAACCTACACTGGAGCCTGAGAAAAATGCTAATTTTAGGAGAACATTTCAGTTTTTGTATTTGAAATCTTCAATTGTTTTATATGTTATACTATAAACCTACAAATTTGAGTGACCATATTTGCATAAATTTGTAAATAATGCAGATAATTTTCCTCAACATCTTAAAACTTCATATCCAAGTCTAAAATTAGAATTATTTGAGTATGATCGAATCTTTTTTTGTCCTTCTCTACTGTATATTATCAGTAATTGTGGTTTGTGGATTTAAAGTTTAAACTCCCTGACTTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21480
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 |
---|---|---|---|---|---|
ENSDART00000083567 | Nonsense | 342 | 985 | 11 | 25 |
Genomic Location (Zv9):
Chromosome 9 (position 24235554)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23391340 |
GRCz11 | 9 | 23202209 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCAAAAACACAGTTTCTGTTAACATGGAGCTCACAGCTGAGGAATGG[A/T]AGAAGAAATATGAGAAGGAGAAAGAGAAAACCAGAAATCTGAAGATCATC
Long Flanking Sequence:
CTGGGGAACGTCATCTCAGCCCTGGCTGAAGGAACCGTAAGTGCTCAACCATTTTTTTCTTCCTCACTGAAATACTACTCATCATGTGTATACAATCTAGGCCACGTTTATCCATCTCAAACAGAGCAAAGCAATATGTTTTCATTGTAAATTATGTATTGGCTTCTCTTTGTCATGACAGAAAACCCATGTGCCGTACAGAGACAGTAAAATGACCAGGATCCTGCAGGACTCTTTGGGTGGAAATTGCAGAACAACTATCGTCATCTGCTGCTCTCCTTCTGTATATAATGAGGCTGAGACAAAGTCCACCCTCATGTTCGGCCAGAGGTCCTCACATTTGATTTCTTTTTATAAAGACTGTAGTTAACATTAGTTAGTTGTGTGGCAACTAATATGTGTGTATATAAATAATTGTATATATTGCTTTGTCTTCACACAGAGCCAAAACCATCAAAAACACAGTTTCTGTTAACATGGAGCTCACAGCTGAGGAATGG[A/T]AGAAGAAATATGAGAAGGAGAAAGAGAAAACCAGAAATCTGAAGATCATCATCCAGCGCCTAGAAAATGAGCTCAAACGATGGAGGAAAGGTAACAAAAACCACACATTCTGTGCCATGATTTACAGAAGACGCAAAAAAAAATCATTTAGTGAATCAGGTTAAGTCAAGCTTTATTGTCATACCACTTCATGTATGGACATACAAAATGTTGAACAAAATGATGTGTCTCGTAGGACAATGGTGCTACATACATTAATCATAAATACAAACACAACACTGGACATAAGAGCTATTTTTATAAAAAAAATTTTAAAAAACTATTTTGTTTATAACCTATTAAACAAACTTTTTATATAGTATATGAAAAGCAAGATGCTTGTACAATTTAAAATATAATTAAAGTTAGTATCATCACTGATTGAGTTATTTGATGTATTTTAAAACCCAGAATGTGAATGTTGTTTTATTTTAAACACAAGTTAGAATCATTAGCCCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8541
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 |
---|---|---|---|---|---|
ENSDART00000083567 | Nonsense | 368 | 985 | 11 | 25 |
ENSDART00000083567 | Nonsense | 368 | 985 | 11 | 25 |
Genomic Location (Zv9):
Chromosome 9 (position 24235476)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23391262 |
GRCz11 | 9 | 23202131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACCAGAAATCTGAAGATCATCATCCAGCGCCTAGAAAATGAGCTCAAA[C/T]GATGGAGRAAAGGTAACAAAAACCACACATTCTGTGCCATGATTTACAGA
Long Flanking Sequence:
TCATCATGTGTATACAATCTAGGCCACGTTTATCCATCTCAAACAGAGCAAAGCAATATGTTTTCATTGTAAATTATGTATTGGCTTCTCTTTGTCATGACAGAAAACCCATGTGCCGTACAGAGACAGTAAAATGACCAGGATCCTGCAGGACTCTTTGGGTGGAAATTGCAGAACAACTATCGTCATCTGCTGCTCTCCTTCTGTATATAATGAGGCTGAGACAAAGTCCACCCTCATGTTCGGCCAGAGGTCCTCACATTTGATTTCTTTTTATAAAGACTGTAGTTAACATTAGTTAGTTGTGTGGCAACTAATATGTGTGTATATAAATAATTGTATATATTGCTTTGTCTTCACACAGAGCCAAAACCATCAAAAACACAGTTTCTGTTAACATGGAGCTCACAGCTGAGGAATGGAAGAAGAAATATGAGAAGGAGAAAGAGAAAACCAGAAATCTGAAGATCATCATCCAGCGCCTAGAAAATGAGCTCAAA[C/T]GATGGAGGAAAGGTAACAAAAACCACACATTCTGTGCCATGATTTACAGAAGACGCAAAAAAAAATCATTTAGTGAATCAGGTTAAGTCAAGCTTTATTGTCATACCACTTCATGTATGGACATACAAAATGTTGAACAAAATGATGTGTCTCGTAGGACAATGGTGCTACATACATTAATCATAAATACAAACACAACACTGGACATAAGAGCTATTTTTATAAAAAAAATTTTAAAAAACTATTTTGTTTATAACCTATTAAACAAACTTTTTATATAGTATATGAAAAGCAAGATGCTTGTACAATTTAAAATATAATTAAAGTTAGTATCATCACTGATTGAGTTATTTGATGTATTTTAAAACCCAGAATGTGAATGTTGTTTTATTTTAAACACAAGTTAGAATCATTAGCCCCTCTTTTTTTTGTTTGTTTAAAATAATTCTCAAATGATATTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGTTAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9450
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 |
---|---|---|---|---|---|
ENSDART00000083567 | Nonsense | 368 | 985 | 11 | 25 |
ENSDART00000083567 | Nonsense | 368 | 985 | 11 | 25 |
Genomic Location (Zv9):
Chromosome 9 (position 24235476)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23391262 |
GRCz11 | 9 | 23202131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACCAGAAATCTGAAGATCATCATCCAGCGCCTAGAAAATGAGCTCAAA[C/T]GATGGAGRAAAGGTAACAAAAACCACACATTCTGTGCCATGATTTACAGA
Long Flanking Sequence:
TCATCATGTGTATACAATCTAGGCCACGTTTATCCATCTCAAACAGAGCAAAGCAATATGTTTTCATTGTAAATTATGTATTGGCTTCTCTTTGTCATGACAGAAAACCCATGTGCCGTACAGAGACAGTAAAATGACCAGGATCCTGCAGGACTCTTTGGGTGGAAATTGCAGAACAACTATCGTCATCTGCTGCTCTCCTTCTGTATATAATGAGGCTGAGACAAAGTCCACCCTCATGTTCGGCCAGAGGTCCTCACATTTGATTTCTTTTTATAAAGACTGTAGTTAACATTAGTTAGTTGTGTGGCAACTAATATGTGTGTATATAAATAATTGTATATATTGCTTTGTCTTCACACAGAGCCAAAACCATCAAAAACACAGTTTCTGTTAACATGGAGCTCACAGCTGAGGAATGGAAGAAGAAATATGAGAAGGAGAAAGAGAAAACCAGAAATCTGAAGATCATCATCCAGCGCCTAGAAAATGAGCTCAAA[C/T]GATGGAGGAAAGGTAACAAAAACCACACATTCTGTGCCATGATTTACAGAAGACGCAAAAAAAAATCATTTAGTGAATCAGGTTAAGTCAAGCTTTATTGTCATACCACTTCATGTATGGACATACAAAATGTTGAACAAAATGATGTGTCTCGTAGGACAATGGTGCTACATACATTAATCATAAATACAAACACAACACTGGACATAAGAGCTATTTTTATAAAAAAAATTTTAAAAAACTATTTTGTTTATAACCTATTAAACAAACTTTTTATATAGTATATGAAAAGCAAGATGCTTGTACAATTTAAAATATAATTAAAGTTAGTATCATCACTGATTGAGTTATTTGATGTATTTTAAAACCCAGAATGTGAATGTTGTTTTATTTTAAACACAAGTTAGAATCATTAGCCCCTCTTTTTTTTGTTTGTTTAAAATAATTCTCAAATGATATTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGTTAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5538
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083567 | Nonsense | 646 | 985 | 17 | 25 |
Genomic Location (Zv9):
Chromosome 9 (position 24222867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23378653 |
GRCz11 | 9 | 23189522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAGCATCAAGCAAAGATCAAATCCCTCACAGACTACATGCAGAACATG[G/T]AACAGAAGAAGAGACAGCTGGAGGAAAGCCATGATTCACTGACAGAGGAA
Long Flanking Sequence:
GAGAGCACGCAGAGCGACACCATGCGTAAAATGCAGGCCAACGAGAAAGAGCTGGCGTCCTGTCAGATGCTGATTTCTCAGGTACACACAAGCAGTCAACTGCGCCCCCTAGTGATCAGTATCCAGACACATGGGCGATTCTTCTCTTTGATCTCCTGATGATTTTAAAAAGAAAGAAAAAATGTAACGGCTCTATTTTAAATGGTTTGTAAGTTTCATTTTTTCACAGCTTTTTTTCTCATTTTAAGAATAGTGATATATAGATTTTTTTTGCAGATTATCTGTTTTAGTTTTCCTGTATACACTTTTTATTTTTGCCCCTATATTAACTGATTAAAGATTGTTACATTTACAAAAAGGTTTTTTAATGTTCTATTCCATTAATATAAGTTCTTAAGCACAATAATCTAAACATTGTTTTTTTGTGTTTTATGTTTTTTTCTTCCTGTGTCCAGCATCAAGCAAAGATCAAATCCCTCACAGACTACATGCAGAACATG[G/T]AACAGAAGAAGAGACAGCTGGAGGAAAGCCATGATTCACTGACAGAGGAACTCGCTAAACTCCATGCAGAAGGTCTTTGTGGTTTAAAATCTTGCTAAATCTGTCACAAAAAAAATGTGGTAATGTGAAAATGAAAAACAAGCACACTTAAAAGTAAGTTTGAACACAGCTATGGATAAACTTAGGAGACCAATTGAAAATAATCTACATTTATAGCAACAAAAATGCCTTTCATAAAAGTTTACAGACATTTTATATTCATTTTTACACAACAAAATGCCAATGTTTTAGCTTTAAAAGAGTTAAGAAATCAATATTTGGAGGAATAAACCTCATTTTCAATCACAACAAATAAAAACATTTTTTTTAAAAAGATTGCTTTAATCGACAATACCATCATTTGAAATTAGAAAGATATTTTACTCAACCCCATACCAAATAAATCCATTAAATCCAGAGGAACTGAACATTTTTAATTGGTTATATAATTTTTCCATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38739
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 |
---|---|---|---|---|---|
ENSDART00000083567 | Nonsense | 947 | 985 | 25 | 25 |
Genomic Location (Zv9):
Chromosome 9 (position 24219079)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23374865 |
GRCz11 | 9 | 23185734 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTGCTTCTCCGGGTCACAGTGTGAGAGGAGGCACGCCAAGCCCCAGA[C/T]GACACCACCAACACCAACCACATCACCACCAACAACCACCCCAACCACAC
Long Flanking Sequence:
GCAGACCTAAGATGTGAGCTGCCCAAACTGGAGAAGCGCCTGCGTGCGACGGCTGAGCGTGTGAAGATCCTTGAGTCTGCTTTAAGAGAAGCCAAAGAAAGTGCCATGAGAGACCGCAAGAAGTACCAGCAGGAGGTGGATCGCATCAAAGAGGTCATCAGAGCCAAGAATCAGTCCAGGAGGAACCACACTGCACAGATCGGTCAGAGCTGCTCCCTCTCCAGATTTCAATACGCTTTTTATCCAGTAGAGGGCGCTACATACTAAACCATCTTATCTCCTGTTATCCAATGATAGAATAATCTCATGCATTGCAGTGCCTGAATTTAGTGCATAATATTCAGTGTTTTATAAATGTATTTAGATTGTTTAAAAATATGTTTTGTTTATATATCTGTGCTTTGTTTCTTATAGCTAAGCCTATTCGTGCTGGACATCATCACCCAGTTGCTTCTGCTTCTCCGGGTCACAGTGTGAGAGGAGGCACGCCAAGCCCCAGA[C/T]GACACCACCAACACCAACCACATCACCACCAACAACCACCCCAACCACACCACCCTCATTACCAACACCAACCACACCACCAACCGCAGCAGCTGCAGTACCATCACAGGAGCAAGTGAAAAACACACCACGTAAGATCATTTCAGCACATCCACATATTTTGTTCTGCAGAAACAAAATGTATTTGAAATGCAATGAATTGTGGGGTTGAGATCTTTTCTTCTTTATTTATCTTTCTGGGATGATAAATCGATTTTTTGTGATTTGTTGATTGATTCTTTGACTATTGATTTGCACCACTATATACTCTTGAGCTTAGTTTTTAACAGTAGATGGTGCTCTAGACTAATTTTTAATCGTGCACTCTTATGCCGAGTTCAGACTGCATGATATTAGCCCCGGTTTTTAGAAATCTCAGACAAATCCCTGAAATCACAGGCAAATAGCTGCTCGTTCACGTCAGTAACAATCACAGTGTGAACTATCAAAGACACAATCTG
Associated Phenotype:
Not determined