ZMP
kif20bb
Ensembl ID:
ZFIN ID:
Description:
Sb:cb152 protein [Source:UniProtKB/TrEMBL;Acc:Q4KME4]
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 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22067 | Essential Splice Site | Available for shipment | Available now |
| sa35243 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22067
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058665 | Essential Splice Site | 418 | 988 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 12 (position 17528215)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 16407973 |
| GRCz11 | 12 | 16456783 |
KASP Assay ID:
2260-5190.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACAGTTTTAAGACACTGAATTGTTTTGTTCTTACATTATTTTGTCCTT[A/T]GGTAGTTGTCCTCAACCCTAAACCAGCTCCAAGCATTGCACTCAAAAGAT
Long Flanking Sequence:
GATCTGAGAGATGTGCAAGGACTCAGAATAGAGGAGAACGCTTAAAAGAAGCTGGGAATATCAACACCTCCCTGTTAACTCTAGGAAAATGCATCAATGCCCTGAGGCTCAACCAAACTCAGTCCAAGTGAGAAAAATGTCCATGTTAATTACTAAATTAATTAGATAAATTTTTCCTGTTAAATATTTCTTTACATTTCCTTTCAAAATTGGGACTAAAACTGCATTAATATGACTGTTTGCACAGGTTTCATCAGCACATCCCCTTCAGAGAGAGCAAGCTCACACATTATTTGCAGGGGTATTTCTGTGGCCGTGGAAAAGCTTGCATGATCATTAACATAAACCAGTGTGCTTCAGTGTATGATGAAACTCTGAACGTTCTCAAGTTCTCAGCAGTGGCTCAGAAGGTCTGCAGGATCCTTTAGTGTCATTATTAACTGAATAGAAGCACAGTTTTAAGACACTGAATTGTTTTGTTCTTACATTATTTTGTCCTT[A/T]GGTAGTTGTCCTCAACCCTAAACCAGCTCCAAGCATTGCACTCAAAAGATCTGCCAGAGATGTGTCCATGATAATCAACAATGCTGACAAGAAGGATTGGACCAGGAGAAGCTCGATTATGGGCTGGGAGATGAGCCTAGAGGACGTGCAGGAAGATGAAAATGATGAAGACATGGATGAGGAAGAGGTGGAGAGTGACGATGAGAGCATAGTGGACAGAACTGTGCTAGAGACTGTGGAAAATCAAGAGCTGTGTGAGGTACTGAATACCTTTTTCCATTTTCATGAATTTTCAGGATTATTTTTCTTAACTATATAATATGCTAATTAATATTTATTTATGCCACAGCTTCAGGTAAAAATTGAAGAACTCCAGGAGAAGCTGATCAAGGAAGAGTCTGAAAAACTAACTTTGGAAGCCCGTATTCGTGAAGAAGTCACCACAGAGTTTATGGAGCTGTTTTCTAACATGGAAAAAGACTACAGGCAAGTTGACCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35243
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058665 | Essential Splice Site | 678 | 988 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 12 (position 17531051)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 16410809 |
| GRCz11 | 12 | 16459619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTATTCAGATGCAGGATTTAAATGACCAACTTCTCCAGGCAACCAGGG[T/A]AAATTGAAATAAAGTTTTCTCCAAGATAAATATCTGATGTTACTGTGAAC
Long Flanking Sequence:
GTGCAGCTGTGTCTGGCCAATGTCCCTGAATCACCTGGAAAACTCAGTCATCTGAGGACAGAATTGGAGGAGATAAAGGCGGAACTTCTGAAAAGTCAACAACAACTCAGTCTCAAATCTAAAGGTGAGTTCAGTTGCCTTAAGGCTAATTAATACTGCAACAGACTTCATCTAAATTTGACAGATCGGTGTGGTACCCCTGCTTGTTTTTTTTCCCAACTGAACATGCTACAGCAGTGATTGCAGAATATCTAACAAGTGACAATCTGGTGATTTTCCATGTTTGTGCCTGACAGTGTTGTATTAAATGACTTTAAAAAAAAAAAACACTTTTTTTGAAAAGACATCTTTTTGTTGTTGTTGTCTTTTTTAATCTATTTTTTGGCTCTCTCTCTATATATAATTAAATTAAAAAAAATAATTCTGTGCATCTCCAGAGTTTGAAGAAAGCTGTATTCAGATGCAGGATTTAAATGACCAACTTCTCCAGGCAACCAGGG[T/A]AAATTGAAATAAAGTTTTCTCCAAGATAAATATCTGATGTTACTGTGAACAGATTGCTATCATTGACCGTGTGGCTTCTGTTAATTTTTGCTTCTCTTAGAATTATGAAAACCAGAAAGTGAGATGTCAGGAACTCATGTCTATCTGCCAGGAGAAAGACGACATGGTATCTAAATTACAAACCGCTTTGGAACAAAATGATGAGGCAGCTAGTAAGGATGTAAGTTTGCAGTACACTGCCATTTTAAAAGTTTGTCTATACAATTTTTGAAGTCTTTAATGCTAAAACACACGTCCACCCACACACACAAAAGTCCCTAGCCTTCCTCTATAAAAAAAAATAATTAATTGTACATGCAGTTACACATTTGGACTATAATAACCTGTCTTTTTGCTCTTGTACAGAGGGCCCTAATTAACAACATCAGAGAAGAAATCCTACATTTCAAAAACAGCTGTAAGTGTAAGCTGAATGAAGAGCATGATGAAATGACAAGTCA
Associated Phenotype:
Not determined