Busch Lab

ZMP

zgc:112061

Ensembl ID:
ENSDARG00000044491
ZFIN ID:
ZDB-GENE-050522-252
Description:
kinesin family member 20A [Source:RefSeq peptide;Acc:NP_001154942]
Human Orthologue:
KIF20A
Human Description:
kinesin family member 20A [Source:HGNC Symbol;Acc:9787]
Mouse Orthologue:
Kif20a
Mouse Description:
kinesin family member 20A Gene [Source:MGI Symbol;Acc:MGI:1201682]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa29638 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32355 Essential Splice Site Available for shipment Available now
sa7483 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa29638
Status:
Mutation detected in F1 DNA
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
ENSDART00000065337 Essential Splice Site 139 921 4 19
ENSDART00000124273 Essential Splice Site 139 921 3 18
Genomic Location (Zv9):
Chromosome 21 (position 33887251)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 34886944
GRCz11 21 34921434
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGAGAGAGGGGTCGCTCAAAGTGTGCACAAATTTACATTTACAAAGG[T/C]AATGGACACAAACAAATATAGACTGGTCATGGAATATTTGGAAAATCATG
Long Flanking Sequence:
CCCTCCCTCAATAATTCTTTTCATTGAAGACAGCAGTAAGTGATGTGTTCTGTTCAACACAAACAGCTTGTTTAATGGCTATTCCTTCACCTCAGGCTTTGTTTGGGTTCAGTGTGAGTGCTGTAATATTAATGGATCTTTTATCTTTTTGACAAACAGCTTGTGCAGATCAAAAGCGATATCAGCAGAAGAGGCAGCACTGATGATGGATCAGATAAACTTAAGGTTTTCCTACGGATCCGTCCTCTTACAGAGGCAGAGAAGGACCGGGGAGAAGAGCAGGTAAAGAAATGTGTCACTTATGTGAAACTATTTTTCTAGGTAACGGAAGGATCTGGCTTAACAATGAAGTGGTTATTGTTTTGTTTGTGCTCTCCAGGGTTGTGTTAATGTGCAGTCTGAGGACAATCTGCTTCTCAAAGCACCTAAAGACTCCCGCAACATGAAGAGTGCTGAGAGAGGGGTCGCTCAAAGTGTGCACAAATTTACATTTACAAAGG[T/C]AATGGACACAAACAAATATAGACTGGTCATGGAATATTTGGAAAATCATGGAGTTTTAAAGTTTATTCCAGGGACCTGTACCATAAAACTGGATCTAAGTGGGTAGCCAGTTTCAGTTTAGTTGGCACCAATCTTGAGTTTTTAGTTAACATGAAAGCAGATCGATTTTAATCACTCTTTGTTACTGTGGTATTATGGAGCAGCTGAGCTACCTTCATTTTACTTAAAATCCAAAATATGTGCAAACTAAACTGAAACATAAGTTATAACTGGCTAGCTAGCGAATCTGGTTTTGTTGCACAGGTTCCTGTAGGGCTGGATGATAAATCAATTTTATCAATTAACTCGAGTGTGAAATTTACATCAATTTGTTTGAATAAAATCGGTTATCACTCTCGCTCAGTACACTATACTAATCTACCAGATGTGACCTGACACCAATAAAAGCAATGAAAAATGCAACCTAATGTGAATAATTTAAATTAACACTAAATAATTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32355
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065337 Essential Splice Site 185 921 5 19
ENSDART00000124273 Essential Splice Site 185 921 4 18
Genomic Location (Zv9):
Chromosome 21 (position 33884087)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 34883780
GRCz11 21 34918270
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTATACTTACGGTGTGACTAACTCCGGCAAAACCTACACCATACAAG[G/A]TAAGGTGGCTGCTTAATGCATTTTGGATTTTGGCGCATTATATTTCTGTA
Long Flanking Sequence:
GTATAGAGCATAAAAATGGCCCATTTTTCAATATTGGGCTGAACAGTTTTGTCAACCTGCCAGATTTTAAATTTCCACTGTTTGCTGATAACGGATCTCTTTATAATGTAATACAAATGTGTCTGTTGTTGCCTTGGTAGCATAAGTGTAATGTAAACAGCAATATGGACGTTAATCAGATATTTCTCTTCTTGAGACTCTTATCTGATATTTGTTCTTTGAATGGTTCAGCACTATAGTGGAAAATCGCTAAACCCATTTATGCTCAAGTTGCCTTCAATGATTTCTTTTTTTTCAGTCTTAAGTGACCAGTTTGAAAGAGTTCTAAGACTGTGAATTTAATAGTTTATCATTTGTGCAGATTTTTGGACCACAAACCTCTCAGCAGGAGGTTTATGATCACACCATTCGGGAGATGGTGCGAGATGTTCTACGTGGAGAAAACCGCCTTCTCTATACTTACGGTGTGACTAACTCCGGCAAAACCTACACCATACAAG[G/A]TAAGGTGGCTGCTTAATGCATTTTGGATTTTGGCGCATTATATTTCTGTAAGGTTGGAAAGGTTACGGTAAGAGAATTGGTGTTGCTGTGATTGAACAGGGGCAGGTGCTGAGGCAGGTCTTCTGCCAAGGGCTTTAGTGTCTGTATTCCTGAAGCTGTCTGGTCGGCTGTACACTGCCATGGACCTCAAGCCTGTTCTGAGCCAGGAAGTCCGTAAGCTAGATGTTGGTGAGGTCCGTGCTGAGGAAATGCGTCGTGATGCTTTACTAAAAGAGGTAAACAGAAGAATGGCACAAATAGAATGGGTTATGTAATTTTTACTGATGCATATTTTGACAATGCTCAACAAACCTGTCTTAACACATTGACAATATAGCACAGCCATTAACTAGTAGTTTTAGCAGGGCTATTTAACTATTATACGTAATGTATTTTTAATCAAGTCTTCTCTTTACACATTACAGATTTGGCAAAGATACATTCATGAGATATAATTTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7483
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065337 Missense 504 921 12 19
ENSDART00000124273 Missense 504 921 11 18
Genomic Location (Zv9):
Chromosome 21 (position 33863427)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 34863120
GRCz11 21 34897610
KASP Assay ID:
554-4280.1 (used for ordering genotyping assays)
KASP Sequence:
GGTGAACATCAACCCYTGTGCCTCCACCTATGATGAGACACTCCAAGCAC[T/C]CAAATTCTCTGCWATTGCCACACAGGTGAAAATACTCTTCATTTTTCTAT
Long Flanking Sequence:
TTTGTAATTGCATAATTAAGATGCTTGCATTAATTGCTGTATAACTCTCAAAGTTTTATAACTATTCTCATATTTTAGTGAAAATACTTAGCTATTTTTGTGTTTGTGTGTTTTTTTTCCCTGACAGACTCTCTGTATGTGATTTGGCTGGGTCTGAACGCTGTAAAGCACAGCAGAATGGTGAGAGAATGAAGGAGGCAAACAACATCAACACCTCTTTGCTGACACTAGGCCGCTGCATCACTGCTCTGAGACACAATCAAACCAACAAGTGAGTGTTGCACTTTATGAAAGCATCATGATGGTCCAGCAGTTATCTTATTGATAAGTGAGGTCACTATACTGACACTGTCGCAGGTCTCGACCACCAGTGGTCGTTCCATTCAGAGACAGCAAGTTAACCAGGGTCCTCCAGAGTTTCTTTTGTGGTCATGGGCGCTCTTGCATGGTGGTGAACATCAACCCTTGTGCCTCCACCTATGATGAGACACTCCAAGCAC[T/C]CAAATTCTCTGCAATTGCCACACAGGTGAAAATACTCTTCATTTTTCTATAAATATGTTTCAATTTCCTTCCATGACAGCTAACTATAGGGTTTGTATAAGTGCTGCAAATATTTGAAAAATCTTAAATCATAATTGATTGTTTTCAAAATTAGACTTTTGGGTAAAGTGCTCAAATGTTATTGTTGCTATTATTGGGTTTGGGGCAAACATGCCATTAAAATTTTTCTTGGTTACTTTGAAATGGCATTTGATATAATGTAGTATGGAGTATGCATATGTATGTTAGGCATGGGATGATAACCGGTTTGAAGGTTTACTGTAGGGCTGGGTGATATTTAAAAAAAAATCACTTTATCTTTTATCACTGTCTTTTATCATTAGATATCCATAATTATTGAACATTTTTTAAAATAAATTTAGGAATATTAGGAATTTTTGTTATTTAACGACTTCATTTTATTTGACCAACATTACTAAAGCAAATAGTTTTAATAGTCA
Associated Phenotype:
Not determined