ZMP
KIF13B (2 of 2)
Ensembl ID:
Description:
kinesin family member 13B [Source:HGNC Symbol;Acc:14405]
Human Orthologue:
KIF13B
Human Description:
kinesin family member 13B [Source:HGNC Symbol;Acc:14405]
Mouse Orthologue:
Kif13b
Mouse Description:
kinesin family member 13B Gene [Source:MGI Symbol;Acc:MGI:1098265]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37167 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9347 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23817 | Essential Splice Site | Available for shipment | Available now |
sa3078 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37167
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 |
---|---|---|---|---|---|
ENSDART00000058858 | Nonsense | 443 | 1097 | 13 | 25 |
Genomic Location (Zv9):
Chromosome 20 (position 50178027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 50063060 |
GRCz11 | 20 | 49866274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGTTCAGGAGCGTCAGAAGCAGCTGGAGAGTTTGGGCATTTCTCTA[C/T]AGTCGTCTGGAATCAGAGTCATCGATGAGAAATGTTTCCTGGTGAACCTG
Long Flanking Sequence:
CACAATATGAAACCTTAAATACCTCTTTTGCACAATATTCTGCACAACATTTTGCAGTCTTGTGTAGCAGTACTTGTATAGCCTGTGTTGTGTGTATATCTAAGTATCTTATAGTTTGTTAGTTATGCATAGGTTTTTTAAATAGCTCTTACATGCATTTCCTGTGTTGTGTTTGTATTTATGATTAGTCAATGTACTGTAGCACCGTTGTCCTGCGAGACACAACATTTCGTTTTTCTGAACTTCCACACATGTAGCGGAATGACTAAAGGTCGACTTGATTAGTCTTGAACACCTTAATTATTTGGATCAGGTTTGTTTAATTAGTTAGAGCAAAACTGTGCAGTGCTGTGGCCCTCTAGAATACAAGTTTGAGACGTATGTTCTGCACAGTAAACGTGTGACTGCTGATTTTCAGATGCGTTTCGTCTGACTTGTGTAATGTTTGTTTGTTTGTTCAGGAGCGTCAGAAGCAGCTGGAGAGTTTGGGCATTTCTCTA[C/T]AGTCGTCTGGAATCAGAGTCATCGATGAGAAATGTTTCCTGGTGAACCTGAACGCAGACCCTGCCCTCAACGAACTGCTCGTCTATTACTTAAAGGTACAGACACACATTATTTAGGATTATTATTACACGGCTGTTTAGAATATCTGCTTATGATTGGTCAGTGGTGACATTGCAAGGTATGTTATTCCCAGATACCAACTTCTCAATAACACAAGTTCATCCAGGAACTTCCAGTCACCTTGACCGTCAGTAAATACGTTTACATTGATATACTTGCGTTCATAAGTATCTGCTCTTCTATAACACTGCAGTTTTTGACTATTTTGCGATATCTTGTGAATGAATAATATGCAGGTTAGTCAGTGCTTTATTCAGGCGGTTTAATTTCTGTCAGCTTTGTTTTTGACTGTTTGGCGCCATCTTGTGTCTGAATAATGTGCAGGTTAGTGTATACTCCATCAGCTGTTTTCGTTTCTGTCAGATTTGCATTTAATTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9347
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 |
---|---|---|---|---|---|
ENSDART00000058858 | Nonsense | 623 | 1097 | 17 | 25 |
Genomic Location (Zv9):
Chromosome 20 (position 50170983)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 50056016 |
GRCz11 | 20 | 49859230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGATGCAGTCAGTGCTTCACTCTCTGGAGCGCAGACATGAGGAGGAGAAG[C/T]GATCTGCTCTGGAGCGTCAGCGGCTCATGTACGAGCAGGAGCTCCAGCAG
Long Flanking Sequence:
TGCTGAAATGTGGCATTGGTGGACTGAGCAAGACGTGATGTCCCTGTGCTCAGTTGGATTCAGGTCTGGGAAACGGGCAGGCCAGTCCATAGCATCAATGCATTCATCTTGCAGGAACTTCTGACACACTCCAGCCACATGAGGTCTAGCATTGTCTTGCATTAGGAGGAACCCAGGGCTAACCACACCGGCATATAATCTTACAAAGGGGTCTGACGATCTCATCTCAGTACCTAATGTCAGTCAGGCTACCTCTAGCAAGCACATGGTGGACTGCGCGGCCCCCAAAGAAATGCCACCCCACACTATTTATTACTGACCTAAAACTAGCAATGTGAGCTAACAAAATCAACTAGTTTTAATTCAATTTGTACTTTAACATTTAAAGTTTTTCCCCATCAGTCTTGTGATAATTACATTTCGATCTGAATCTCCTCTTTCCTCCAGACCCGATGCAGTCAGTGCTTCACTCTCTGGAGCGCAGACATGAGGAGGAGAAG[C/T]GATCTGCTCTGGAGCGTCAGCGGCTCATGTACGAGCAGGAGCTCCAGCAGCTGCGCAAACGTCTGTCTTCAGAGCTGCAGACCCAGAGCTCGCACCCGCAGCACCACCGCAGCAGCGAACAGCTCAACGCCAGCGCACTGTCCTCTCAGAGCCGCCTGCGCCAATGGACTGACGACAGGTTAAAAAAAATGCATATACACTAACCTACGAAATATTCACATGCTGCACCTCAGAGTAGACGTGTGCTGATGTTCAGTAATTTCATTCTAAAGTACATCCAGGAGGTTGTTATCTCAGAATAAAGCCTGATAAGTTTCAGCAGAAGACTGAAGGGCTTTATTCTGTGAAAACAACCGCCTTAATGTACTTTATCCCATTTATTACATGACTACTTGCTACAAAACATACAAATTAAACACAAAACATGGTTCTGCGCTGTAATAGTTTATTAAATTTTGTTTTACATGCAAATTAGACAGAAAAAAACGTGATGGAGTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23817
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058858 | Essential Splice Site | 933 | 1097 | 22 | 25 |
Genomic Location (Zv9):
Chromosome 20 (position 50157405)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 50042438 |
GRCz11 | 20 | 49845652 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAGCAGTAGAGAACCACAGAGTCTGGTGGTGTTCGACAACTGCAAGG[T/C]CTCAGTTCATCACAAAAAACACTACATTTGTGCCATTTATTTCTCTCCTT
Long Flanking Sequence:
CTTTTGAAAAACCCATTTTCAAGATTTGATCCAATCCCTTATCCAAAATCCTAGTGGATTACTTTTGAAAAACCGGGCCCAGGAGTCATGGATATTGATTTGAACTCATTTGTATGCGATTATTTTTAATCTATAAAACCTGTCACCATTCACTGCCATTTATATGAAGAAAGAAATGCATCTAAATCTTAGATGACTTGTGGGTGAGGAAACTGACAGAAAATATTTATTTTTTGGGTGAACTATCCCTTTAACTTAATTTAGACCAAATGTGCAGTTACTGCAATGTAGGGTAGAGGTGTAACTTGGCTTTCTCTATATTTCTTTCCAGATCAAGGTGTTGCAGGCCACGGGTCTTCCTCAGCATCTCTCCAACTTCGTGTTCTGTCAGTATCATTTCTGGGATCAGCCGGAGCCAGTGTTCATCGCTCCTGAAGTGGGTCTGTCCGCTGCCAGCAGTAGAGAACCACAGAGTCTGGTGGTGTTCGACAACTGCAAGG[T/C]CTCAGTTCATCACAAAAAACACTACATTTGTGCCATTTATTTCTCTCCTTCTGTATTTTTTTTCTTATTTCTTACAGTTTAAAAAGTCAACAATGCACATAACGCACACAAACTATCTAGATCAGTGGTTCCCAACCTTTTTCTTTGCCCCCCCCTATATATATATATATATATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNACACACTCACACACTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTGTATGTGTGTTTGTGTAATATCAATATATAATATGTATAGAAAATATAAATTAATCAGTTTTAACTTGTCTTGGCCTTCAATAAAACCAAAATTTAGGTAGGCTTTGTCATACTGTCTAATCTTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3078
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 |
---|---|---|---|---|---|
ENSDART00000058858 | Nonsense | 984 | 1097 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 20 (position 50154867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 50039900 |
GRCz11 | 20 | 49843114 |
KASP Assay ID:
554-3036.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTGGCTCTCTGGGACCTGGGGGTGATTCAGGCCAAGACTCGCTCTCTC[A/T]GAGAAAGGTATATTTGCATTCTAGATTTTTATTGAATTTATATATATATA
Long Flanking Sequence:
ATTGATTTAAAAATTAAAAACTACTTTTATTCTAGCCAAAATAAAGTATGTAAAGTAAGACTTTCTCTAGGAGACAAAAATATTGTAGGAAATACTGTGGAAAAATTCCTGAATCTGTTAAACATCATTTGGGAAATATTTGAAAAAGAATAAAAAATTCACAGGAGGGCGAATAATTTTGACTTCGACTGTATATATTGATCACTTAATAATTTTTATTGCTTTAATTTCCACGTATTTAAATGTCTTTGTGTTCTTGTTGATATGTATGCATGCATGTATCCTGAGCTCCTCGGATTCAGATTTTCCTCTTTGTGTACTTTTTGTCACGTCTTTTTCTGCATCTGTAGACTCTGGAAGTGGCTGTAACTGAAGACTTTCAGGAGTTTCTGATGGAGGGAGCTGTGGCTGTGGAGGTTTATGGTCACAAGCAGGAAAATCCACGCAGGAATCTGGCTCTCTGGGACCTGGGGGTGATTCAGGCCAAGACTCGCTCTCTC[A/T]GAGAAAGGTATATTTGCATTCTAGATTTTTATTGAATTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATGTATATGTGTGTGTGTGTGTGTGTGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAAAATTTAGGTAGGCTTTGTCATACTGTCTAATCTTTTTCTTCGCCTCTGAAGAATCAATGCATTTCCGTTTGTCTGCCATTTTTGTTTTGATTTTGCCTTTACGACACGTTGACAAGCAGATTGCGCGAGTGAGCAAAATTTAAATAATTATTTAAAGTTATTTATTTTAATTATTTTCACTATTATGTTGGAATTTTAAGCATGTGTTTAGATTTTTTTTTGGTACTTA
Associated Phenotype:
Not determined