ZMP
kif11
Ensembl ID:
ZFIN ID:
Description:
kinesin-like protein KIF11 [Source:RefSeq peptide;Acc:NP_775368]
Human Orthologue:
KIF16B
Human Description:
kinesin family member 16B [Source:HGNC Symbol;Acc:15869]
Mouse Orthologue:
Kif16b
Mouse Description:
kinesin family member 16B Gene [Source:MGI Symbol;Acc:MGI:1098240]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15737 | Essential Splice Site | Available for shipment | Available now |
sa12364 | Nonsense | Available for shipment | Available now |
sa36376 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15737
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 |
---|---|---|---|---|---|
ENSDART00000024194 | Essential Splice Site | 434 | 955 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 17 (position 19318683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19468694 |
GRCz11 | 17 | 19488530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTACRGAGTACACTGAGCGSATWGCTGCTAYGGAGGAKGAGCTYAAAAAG[G/A]TGCGCATCTTTNNNNNNCMTTCTACTTCTGCTTTTCTTTTGGCAACTTCY
Long Flanking Sequence:
CCGAAGGAAACCCACGCGAAGGCAGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGAGCCGAGGTTCGACCCAGCGAACTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCCTCGCCCCTCAAACGGAACCAAAAACATCCAAAAACCAGACAGTCACAAAATGTGTCCCTAAAAAGGACAGTGATCAAGCATGAATGGTTTATCTCCTCATAGTTGTGATGTTGAATAGCTGAAGAAGTTAAAAAGCCTTTGATTTGCCATTTAAAAATTATCATGTAAACAAGAGGCTGACCAGAACTAAATATAGTTCACACACAAAGTTCAGAATTGTTATTCTACCCCTTTATTTTAGTTTGATTGAGTTTAGTGAGCGGCTTATTTTAACCTTTTTTTGCAGGACTTTGAATGGTAAAATTGTGTCTCAGGAAGAGCAGATTACAGAGTACACTGAGCGGATAGCTGCTATGGAGGAGGAGCTCAAAAAG[G/A]TGCGCATCTTTTAAATCCCTTCTACTTCTGCTTTTCTTTTGGCAACTTCTGCTTCTGAGTGAGTGATGCATCTGATATATTTTGTGCTTGTGTTGCCAGATTATAGACCTGTTCACAGATAGTAAGCAGAAATTGGAACAGTGCACCGAGGACCTGCAAGACAAAAACCAGAGACTGGAGGAGGCTCACAAAGACCTATCGGAGACCAGGCACCGCCTCAATCAGGAGGAATTCATCAGTACACAGCTTCAAACCAATGAGAGTCACCTCTATAACACTGCTGACCAGGTCTGTGATGCTTGAAGGAATCAGAGTGCATGTCTGGTCCAATAATTTATACTATCGTAACGTTTTATTTTCCTTTTTTTTTTTTCTCTCTCTCTCCTCATTCTATCCAGTTGTTGAGCACTGCTGAGGCCAGCACACAGGATGTCGGTGGTCTCCATGCTAAGCTACAAAGGAAGAAGGATGTGGAGCTTCATAACAGTAAGGTTCAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12364
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 |
---|---|---|---|---|---|
ENSDART00000024194 | Nonsense | 517 | 955 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 17 (position 19319139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19469150 |
GRCz11 | 17 | 19488986 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACTGCTGAGGCCAGCACACAGGATGTYGGTGGTCTCCATGCTAAGCTA[C/T]AAAGGAAGAAGGATGTGGAGCTTCATAACAGTAAGGTTCAGGAGAGCTTC
Long Flanking Sequence:
AGTACACTGAGCGGATAGCTGCTATGGAGGAGGAGCTCAAAAAGGTGCGCATCTTTTAAATCCCTTCTACTTCTGCTTTTCTTTTGGCAACTTCTGCTTCTGAGTGAGTGATGCATCTGATATATTTTGTGCTTGTGTTGCCAGATTATAGACCTGTTCACAGATAGTAAGCAGAAATTGGAACAGTGCACCGAGGACCTGCAAGACAAAAACCAGAGACTGGAGGAGGCTCACAAAGACCTATCGGAGACCAGGCACCGCCTCAATCAGGAGGAATTCATCAGTACACAGCTTCAAACCAATGAGAGTCACCTCTATAACACTGCTGACCAGGTCTGTGATGCTTGAAGGAATCAGAGTGCATGTCTGGTCCAATAATTTATACTATCGTAACGTTTTATTTTCCTTTTTTTTTTTTCTCTCTCTCTCCTCATTCTATCCAGTTGTTGAGCACTGCTGAGGCCAGCACACAGGATGTCGGTGGTCTCCATGCTAAGCTA[C/T]AAAGGAAGAAGGATGTGGAGCTTCATAACAGTAAGGTTCAGGAGAGCTTCTCCCAGTGCATGGAGAACTGCTACAACAGCATGCAGACCTCACTGAAGGAGCAGAGCCAAAAACATGCTGCCATGATTGATTATTACCGCTCTTCTGTGGGTAAGATATGTCATGGCCTTTATCTCACTGTTATATCTTGTTTTGGGGCGTTTATAATGTCTTTCGGCAAGAAATGAATGTCTGTTTAATCGTCTCTGCAGGTGAGCTGCTGAACACCAATGGCAAGGTGTTTAAGGAGACTTTGAGTGCTGTGTGCGAGTCTTACAGCAGTATTAAAGGAGCTGTGGGAGAAGGTGTAGAGCGGTGTAAGGAGCAAGTGTTAAATCAGGAGAAACTCTCTCAGGATGCTCAAAACAGCATCCTGGAAATTCTGGTAAGAACAGATGATAAATATTCAAATGGAATATTCCAATCTGCCTTTTTTATTTTTATTCATTTTTTTTTATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36376
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024194 | Essential Splice Site | None | 955 | 22 | 23 |
Genomic Location (Zv9):
Chromosome 17 (position 19326614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 19476625 |
GRCz11 | 17 | 19496461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATGAGAACCTGATATGTTATGAGAATGGAAGGATTCCTTTTTTCAAG[G/A]TAAGAAATTGTAAACATTTTTAATTTTTAAGAAATGATCATAATAGTGAA
Long Flanking Sequence:
ATGGGTATATAAGACAGATATTAAGTACGTTTTTAATTTTTGGCTGAACTACCCTATTAAATCTTAACTCTGTAGCAGGTGATCCGCTCTTCAGTAATCTGATGTTTATCTTTTGAAGGAACGACCCCTCAGCGCAAAGAGTACATGTACCCACGTGTGCTGAGCAGGCCGAGGAGTAGAGAGGAGCTGGAAGAGGAGTTCAGAGCTCAGCAAGAGCAGCTTCAGTCTGAACTGAAGCCGTGTGAGATCGTAATGGAGGTGGAGGAGGAGAAACCTGTCGACCAGGTAACCTGATCTAATGCGTGGAAATGCTTTGATTTTTTAAAAATTCAGTATATTTGAAGATCACTTTTTTGTTTGGACTGTTGTAACCTCGCTTCTGTCTTTAGGACTCTCTGGAGGATGACGTCAGTGTTTCTAGTGATGGAAACAACACTGAACAGTCGTGCTCTGATGAGAACCTGATATGTTATGAGAATGGAAGGATTCCTTTTTTCAAG[G/A]TAAGAAATTGTAAACATTTTTAATTTTTAAGAAATGATCATAATAGTGAATTTTGACCACACTTTTCTAGCGTTGTCAGATAATTAATACACTTATTGATTGATTTTTTTTTTTTTTTTTTTTTTTTTTGTTTAACCAGAAGAAAAGCAAGAAGGAAAATGGCAGTAAATCACTGAACCGTTCAAAGGTGGAGAATGACAGCATGTCAACACCACCCCGCTCTAAACTTCCACTCAGATGTCAGAATTAACCTAAATTATGTTGCCAATATTACTCCCTTCGTGTATTAATCTTCCAAGTCCTTTTGTGTCTTAAACGTTGCATTTTTTTAACTATGTCTTTTTTAAACATCGATTATCAATGTATTTGTCTTATGTCTGTCCACACAAGTCAGTTATAACTTCAGGGTGATTTCGTACTGTTACTTTTCCTGTTTCACTAGCGTTTAGGCTTGTTTGTATTTGTTCAAGGTTTTGTATGTTTAATTGAAGACTAAAAGA
Associated Phenotype:
Not determined