ZMP

ENSDARG00000086305

Ensembl ID:

ENSDARG00000086305

Human Orthologue:

KIF9

Human Description:

kinesin family member 9 [Source:HGNC Symbol;Acc:16666]

Mouse Orthologue:

Kif9

Mouse Description:

kinesin family member 9 Gene [Source:MGI Symbol;Acc:MGI:1098237]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18261	Essential Splice Site	Available for shipment	Available now
sa28855	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18261

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
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Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000122415	Essential Splice Site	27	506	1	10

Genomic Location (Zv9):

Chromosome 17 (position 23835108)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	23988550
GRCz11	17	24006951

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCTGCAAGAGACCAAGATGCTGAAACGCTCCCTCACCATATTCGGAAATG[T/G]TAGTAAAACCTCAAACATGTCAGCACACACTCACAAAAAAGCAYGTACTA

Long Flanking Sequence:

TCAGTCATGAGCGCACGCTTTGAGAGCCTTTCTGAATGAATAAATGAAATACGCTGGAACATAATTGGCTAAACTGGCATTGGGTGATTTAAAAGAACCAAAACAAAGACAGACGTTCTGTTTTTGTGCTTTAGAAGAATGAAAAACTTACATACAGCACCTTTAAGAAAAAATGATATTGCAAGTAAAATAAAGCAAATAAAAAGTCATAATTAGCTGTTCTACTTTTTATGCTCTGAAAACTTCAATTAACACTTAATGGGAAAACAATTTTCTTAGCCGTGCTGTTTTACCAAATATCAGAAACTCTTAGATATTTATCAGTTTTATATGACAAATACCAGTTTCGGTTCTATTGTTCACTTTCTTTCTTTTTCACCCACTGCTTCATCAGTGTCGTGCTTCTGTGGTTTCTGACATGAAGAGAACTTTCAATGCCACAAATGAAAACCTGCAAGAGACCAAGATGCTGAAACGCTCCCTCACCATATTCGGAAATG[T/G]TAGTAAAACCTCAAACATGTCAGCACACACTCACAAAAAAGCACGTACTATCCTATTATCGATGTTGTCCCGGTCAGACAGAGGGCATTTTTGAAGAACAGTCATTGTTTTGAGTATCCCAAGACGTACTCTAGTGATTATTTATCAGTGTAAGGACCGTATCTTAATCATATCAATGTGTTGGCTGCATATGCAGGAAATTAGACCCAGGAAATGATCTGTAGGGTTACATAGCTTTCCATTTAGGGAAGGGGGACTTGTCATGTCATATCTAACACAGAGAAAATTATTTCTGCAGAATACTGGCCTTTTTGTTTGCTTATTTACATTTAGATAATGCCGAGACCTCTTCTTCCTTGCTTTGAAATTTCTCACTGCCAAAAAATTCTGTCATTTTAGATACAAATCCAATAAAATGATTTTGGTATACCTAATCTAGTAGAAAATGTGCAGTAATTAAATGCATTACAATAAAAAAATGAAAAACCTATTATGTTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28855

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000122415	Nonsense	294	506	6	10

Genomic Location (Zv9):

Chromosome 17 (position 23840848)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	23994290
GRCz11	17	24012691

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGAGACAAAGACTCACTTAGTCAAAAAGTAGCAGAACTGGAGGATGAGT[T/A]GAGGAAGAGAGAAACTCAGGAGAGAGAAGAGGCAATGAGCTGGGAGAAGA

Long Flanking Sequence:

ACTCGGCTTAAGTCACTGTGCGGATGGACCGGAGCTCAAAACCTTTCTCCCCCAGCTGGAGAAACCAGGCCAAGCAGACCCACCGGGGCATAACAGACGCAGCTCTCGACCTGTAGATGAAATTAACAGAACTGATGGTAGCAAAAGCAGCATTATCGGTTTTATAATGACTTAAATCAGGAATCACTAAACTTGAAATCTGAACCTCTCTACAGGTAGAATGACCCGCTCACTGTCTCGTTGCCTGTCTAGTGCAGTTCTCCATGATACTGGAGGGAGAGACAGAACTGGAAAGACACTAGAGTTTTCATCTGCACAGCGGCGGTCTGTTGAACGTCTCTCCATATCTTCTCTTGAACCTGTGTCATCTCCAGCAGCTGTGGAGTGTCCAAACTGCACCCGCGAGCGGAAGATCAGAGAGGAATACGACAAGATCATTGTTCAGGCAACAAGAGACAAAGACTCACTTAGTCAAAAAGTAGCAGAACTGGAGGATGAGT[T/A]GAGGAAGAGAGAAACTCAGGAGAGAGAAGAGGCAATGAGCTGGGAGAAGAAACAAAGGGAGGAAGAATCCAGCAGCAGTACATCTGAGGATCAAGGAATATTTCAGACTGCTGAGGTAAAACACATCAGAGCATCTAATCCATGTCATTTTGTTTCTTTAGAGGAGTCCGGCGATTTTAAATTAAACTGTAGGTTTACTTTTTAGAAAATAGGAAAATGATATTCTCTGGGGAGAGCTCAGTGGTTAGCAATGTTGCCTCACAGTAAGAAGGTTGCTGGTTCGAGTCCCCCTGTGTGGAGTTTGCATGTTCTCCCTGTTTTCATCTGGGTGCTCTGGTATCGCCCACTGTCCAAAGACATGCGCTATAGGTGAATTGAATAAACTTAATTGGTCGTAGAGTATGGGTATGTGTGAATGCGAGAGTGCATGGGTGTTTCTCAGTGCTGGGTTGCAGCTGGTTGCAATCTTTTGCGCAAAACATATGCTGGATAAGTTGGTG

Associated Phenotype:

Not determined