Busch Lab

ZMP

KIF13B (2 of 2)

Ensembl ID:
ENSDARG00000073859
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
sa23817 Essential Splice Site Available for shipment Available now
sa3078 Nonsense Available for shipment Available now

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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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