ZMP
ENSDARG00000071009
Ensembl ID:
Human Orthologue:
KIF20B
Human Description:
kinesin family member 20B [Source:HGNC Symbol;Acc:7212]
Mouse Orthologue:
Kif20b
Mouse Description:
kinesin family member 20B Gene [Source:MGI Symbol;Acc:MGI:2444576]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36402 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa5901 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa972 | Nonsense | Available for shipment | Available now |
sa28850 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32150 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36402
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104718 | Essential Splice Site | 64 | 1683 | 2 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 23301778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23451927 |
GRCz11 | 17 | 23471951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGATAAGACCATTTTCAGCAGTTGAGATTGAGAATGGAGAATCACAGG[T/C]TAAAGATATATTCATATTTATTTATTTTTGCAGTGTATTGCACAACTTTC
Long Flanking Sequence:
GGCTTTTTTTCTCCCTATACAGTTTCATGACATCTTATTTGTTTATGCGTTGTTTCAGATCAAGATGATGGAGTCAGGGCTAAAGGATGATCCAGCAAGACCTGCTATATTAGTTGTAGAAGATCTAAGGAGAAATTTGTCCACAGAGTTTGATTGTTCAGATTTGCAGGTAAGATGGCAAATTTAGGTAAATTTGGTTTTATATTCGCACATTTGGAATTTCTTCTTAAGAATTAAATTTCATAAATTTATTCTTACAATGAAATACTTATAATGTTGTTTTGAAGTCATTCTTGTATTATATAAGTATTAATAAGTGAGTGTTTATTCAATCATTATGTTTTTGAGTACCCACTATGTATGCTTTTGTTATTTTTGATGAAATGTTTGAGCTGTAATGTTACTTTTTAAGGACTCGTCAGACTTGAAGGAACATCTGAAGGTGTATCTTAGGATAAGACCATTTTCAGCAGTTGAGATTGAGAATGGAGAATCACAGG[T/C]TAAAGATATATTCATATTTATTTATTTTTGCAGTGTATTGCACAACTTTCCAGTGCCCACTCTTTTTGAGAAGAAATGTTTTTTTAAGCTTGGGGAGACATTTTTCCTGAAAAACTGTTGTTAATATTTCAAATGTATCTGTTTCTTCTCTCTGTTTTTGAAGGACTGTGTGACCATTCAGCGTCCAGACACTGTCCTTCTCAAACCTCCACAAACATCTCTGTCTGCCAGGCTCAGTGATAAATCAGTGCCAGTTACAGCTCAGCGTTTCCAGTTCTCTCAGGCAAGCAGACGCATCAACACAGTCCTCCTAAATAATAATCGCTGAAACAAGCCAATATCTTTGTTAAATCTTAAATATTGTGGTATTTTTAGGTCTATGGTCCAGACACTACACAGAAGGATATATTTGATGGCACAGTAAACGGACTTGTCAGAAATGTTCTAGAAGGGCAAAATTCTCTGGTCTTTACGTATGGTGTCACCAATGCTGGGAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5901
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104718 | Nonsense | 420 | 1683 | 11 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 23305849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23455998 |
GRCz11 | 17 | 23476022 |
KASP Assay ID:
554-3912.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCCTTTCAGACAGCATGTTCCGTTCAGAGAGAGTAAACTCACTCACTA[T/A]CTGCAGGRCTACTTCACAGGCCGGGGCTCAGCCTGTATGATTGTAAAYAT
Long Flanking Sequence:
GCAACTTCCTGTTGTTCATCCATTTTTGCATAGTGGGCCCATTTGCACCTGATTTCATGTCCATATCTACTTTGTTTGATTTCTTTTCTTAGCCACAGTATTTTCTCTGTTCGAATACTGAAGGTGGAGGATGTGGGAATACCTAGAGTGGAGTCAGTCAGCGAGTGAGTGTCTATCTCTGCATGGTGTTTGGGTTGTGCCTAATGGTTTGTAAAGTAAATATTCTCCTTCCAGGCTGGCACTGTGTGATCTGGCTGGATCAGAGCGTTGTGCTAAGACTCAAAATAAAGGTGAACGGCTAAAAGAGGCTGGCAACATCAATACTTCTCTGCTCAGTCTTGGAAAGTGCATTAATGCACTAAGGAATAACCAACAGGCTAGGTATACAAATTTTCTTTTTTTTTCTTTTCTTTTTCCTCCTCTGTCTTTTAATCATTCTTTTTTTATGTGTGTCCTTTCAGACAGCATGTTCCGTTCAGAGAGAGTAAACTCACTCACTA[T/A]CTGCAGGGCTACTTCACAGGCCGGGGCTCAGCCTGTATGATTGTAAACATTAATCAGTGCTCCTCCATGTATGATGAGACGCTGAATGTGCTCAAGTTCTCTGCCGTGGCTCAGAAGGTTTGTGACACCCTATTAGGTTTTGATCTCTCTCGTTTAAGTTCTGTCATCAGTTATTCAGCCGTGTGACTTTTCATCTGTGGCTTTAGGGCACCTGAGATCTATTTAATAGAAACAGAATTTATTTTCATTTGCATTTATTTATTTATTTATTTATTTATTTATTTTCTACAAACAACTCTTAATCAAAATTATTTACACAGATCCATGTAAAACACAAAAAATGCTGTATTATGCATTCCAGAAAGGAGGTGATCTCATTACTGACATGTCAATTAATGTAACCTCATTTTAATAATTTATCATTTTTGATATGTAAAATGAAAAATGAGATTTTGAGACATCAATTGTAAAAATAAAAGCTTTAAATAATTTGAGAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa972
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104718 | Nonsense | 813 | 1683 | 19 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 23312895)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23463044 |
GRCz11 | 17 | 23483068 |
KASP Assay ID:
554-0877.1 (used for ordering genotyping assays)
KASP Sequence:
TACAYACCTTATAAAGTTTTCTCAATTCTTTGTAGRCCCCCCGGAGGACT[T/A]GAAAATGCCTRAAGATGAAGCAGATGATGGGCGGGAAGACTCCGCCCTTC
Long Flanking Sequence:
TACTGTTTTTATGAGCTCGACTGAATAAAGTATTTTTATTTTGCACATGGAGAACATTGCACAAACTTAAAAGCACTGTAGGTCATATAAGAACATGCAGTGTCAAGGATGCTTCTATTTCCTCTCAAAAAGAGAGGAATGTTTCTCATGATATCAAAGTGTCCCAGACACACATGAGGTGCTTCCTGAGAATAAACAGGAAGCTTTCAGACTGAGTGCTTCCAATTCTCTTTTATCTTCAGATTGAACATTTATTTTACTGCCCGATGTGCAAGTAGTGCACTCTAGATGAAATTAATTACTGGCTTTGTTGCCAGACCAATAGTAGTAAATATGCTTGGTTGTACTAAGCTAATCTGAATGTCAATATGAATTTGTTAAATGATCTATTTTGAGACCATACACAGTAAAATTGCATGCCACAGACACATCAAAACCAATATAAATATATACATACCTTATAAAGTTTTCTCAATTCTTTGTAGGCCCCCCGGAGGACT[T/A]GAAAATGCCTGAAGATGAAGCAGATGATGGGCGGGAAGACTCCGCCCTTCATGAGGTCAAAGGTCAGCTGGAGTGTTGCCTTGCTGAAGCCAAACAAAAAGACAAGCAGATCACAGACCTTGAGCAGGAATGCCACAGATTACAAGTGTGCATTCAGGATCAAAAGTCAAATCTGGATGAAAGAGTGTCACAGGAACATATTCTGAAAGAAGACGTTTGTCAGACAACATTGGAAAGCAAACAGATGGCAACGGCTGTGGATTTTAGCAATCTGAACGTAGCAGTTGCATCCAGATGTAGCAACACTACAGGTGCGTTTGCTGCTAAATCACTAATGGCTAAGCGAGATCTTGAACTGAGAGAAAAGAACAAACACATCTTGACTCTTGAAAAGGAAATTGCGCTAATGAGACAGAAAGCAGAACACACATCTGACTATGAAAATCTCAAAAAACTCAACTCTGAACTGCAAGCTGAGGTCACGAGCTTATGTAAGGTCA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa28850
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104718 | Nonsense | 937 | 1683 | 19 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 23313266)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23463415 |
GRCz11 | 17 | 23483439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTAAATCACTAATGGCTAAGCGAGATCTTGAACTGAGAGAAAAGAAC[A/T]AACACATCTTGACTCTTGAAAAGGAAATTGCGCTAATGAGACAGAAAGCA
Long Flanking Sequence:
AATTTGTTAAATGATCTATTTTGAGACCATACACAGTAAAATTGCATGCCACAGACACATCAAAACCAATATAAATATATACATACCTTATAAAGTTTTCTCAATTCTTTGTAGGCCCCCCGGAGGACTTGAAAATGCCTGAAGATGAAGCAGATGATGGGCGGGAAGACTCCGCCCTTCATGAGGTCAAAGGTCAGCTGGAGTGTTGCCTTGCTGAAGCCAAACAAAAAGACAAGCAGATCACAGACCTTGAGCAGGAATGCCACAGATTACAAGTGTGCATTCAGGATCAAAAGTCAAATCTGGATGAAAGAGTGTCACAGGAACATATTCTGAAAGAAGACGTTTGTCAGACAACATTGGAAAGCAAACAGATGGCAACGGCTGTGGATTTTAGCAATCTGAACGTAGCAGTTGCATCCAGATGTAGCAACACTACAGGTGCGTTTGCTGCTAAATCACTAATGGCTAAGCGAGATCTTGAACTGAGAGAAAAGAAC[A/T]AACACATCTTGACTCTTGAAAAGGAAATTGCGCTAATGAGACAGAAAGCAGAACACACATCTGACTATGAAAATCTCAAAAAACTCAACTCTGAACTGCAAGCTGAGGTCACGAGCTTATGTAAGGTCAAAGCCGAACTTGAGGAGAAGATTACATGCCTTCAGAAGGAGAAGGAGGGGCTTGAAGATAAGGAGGTGGGGCTGACAAACCCTAACACTCTTGGATTTAAAAGTAAAGAGAGAGATAACCAAACACACCTCATGCTGTCTGGAAAGGAGGCTGAACTTGCACTGAGAGAGAATGCTCTAACTTTAAAGGAAACTCAGCTTTCAGCACTACAGAAGAGTCTGAAGCAAACACAGGAGCGTCTGGAGGAGGAGGAGATGCAGGCGGTGCAGGAGGCGCGCAGGAAGGAGGTGGAGAGGAGGAGAGAGATCCTGGCTGTGGCAGAGGAGGCCATCGCTCAGAAAGATGCAGAGCTACAGAAGAGACAAGTAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32150
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104718 | Nonsense | 1308 | 1683 | 25 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 23318455)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23468604 |
GRCz11 | 17 | 23488628 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGGCTTTTAGCTTGCCAATGAGAAGCAGCAGGCAGAACGCAAGAAGTG[G/A]ATGGAGGAGAAGTTGATTCTGATTGGTCAGGCTAAAGAAGCTGAGGAGAG
Long Flanking Sequence:
GTCCTAGTATTGTTTCATTGAACAACTGATTTAAATTACAAATACTAAATATGCAGAGGTGGATTTAGTCACACTATTACATAGCCTGTAATTTTCAGCTTGATTTCAGTATAGGCTGTTTTAGGACTAACAAAAATTTTCTGAAACGTGCAGGATGTTTTGTTGTCCTTGAACACCATAAAATCCAAAAACTAAAATCTAAAACAGACTCATGGTTATGTTGTTAATCTTTTGGACTTTACTGTTTATTTACAGAGCTGGCCAGTTTGAGAGAAATGTTGCCTGAAGAGAGGGACAGGAGTGATTCCAGACCAATCTCTAAAGATGTTTTACAGGCCAGACAGCAGATCACTCAGGCCCACGAGAGCTTACAGGTCCATGATCCAAATGCATTCTCGATTTCACTTAGTGTAAGAAAAGAAGTTTGCTCATGGTCTTTTTCTGGTTCTTCGTGGCTTTTAGCTTGCCAATGAGAAGCAGCAGGCAGAACGCAAGAAGTG[G/A]ATGGAGGAGAAGTTGATTCTGATTGGTCAGGCTAAAGAAGCTGAGGAGAGGCGGAATCAGGACATGAGACGATTTGCAGATGATCGAGAACGGCATGTTCGGCAACAGGCTGAAATGGTAAAGAGAAGAGTGTGCTTTTAAAGTCAATGTCAGGCAGATGTGTTCTAAAGATAATGATTGTCTGTTAATGTTTGTCTATTAGGAGTCTCTGGCTGCACGTCTTAATGCCCGTGAGGAAGAGATGGAAAGGTGGAGAAAGGAGAGAGACACGCTTGTCTCTGCTCTGGAGGTTCAGCTGAAGAAACTCATCATGTCCAATGGAGAAAAAGACCAACAGATCAAGATGCTGCAGTCCAGTAACACTGCCCAAACACCAGAGGTCAGTGAAGGGTCCCTTGCAGCTCTCATAAGTTCCTGCTTTTTCTATTTTTTTTATAAATCTGCAGTCAGTAAGATTTTTCTTTGCTAAATTAATATTTCATTTCACCAAAAATTGGAGC
Associated Phenotype:
Not determined