ZMP

KIFC2

Ensembl ID:

ENSDARG00000053431

Description:

kinesin family member C2 [Source:HGNC Symbol;Acc:29530]

Human Orthologue:

KIFC2

Human Description:

kinesin family member C2 [Source:HGNC Symbol;Acc:29530]

Mouse Orthologue:

Kifc2

Mouse Description:

kinesin family member C2 Gene [Source:MGI Symbol;Acc:MGI:109187]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10867	Nonsense	Available for shipment	Available now
sa36081	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa10867

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000059841	Nonsense	461	558	12	13

Genomic Location (Zv9):

Chromosome 16 (position 18609076)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	16651653
GRCz11	16	16559630

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTGCAGGSAAGCTGAATCTGGTRGAYCTGGCTGGTTCTGAGAGGGTGTGG[A/T]AGTCTGGAGCAGAGGGGGAGAGACTGAAGGAAGCCCAGAATATTAATCRC

Long Flanking Sequence:

GGTCACTGATTCAAATCTCCAACTGGGCCAAGTGTCATTACTGTTCTCATGTTTGCGTAGGTTTCTTTCGGGTGCTCTAGTTTCCCTCAAAGCCCAAAGACATGCAGTATGGGTGAACTGGATAAACTAAATTGACCCTATTGTATAAGTGTGTGATTGAGAGTGTGTGGGTAATTCCCAGCACTGAAGTTCACAAGTTAAGATACTCTCAGTGCTGGGTTGCGGCTGGAAGGGTGTTTATTGTGTGGAACATATGCCAAATAGTTGGTGGTTGATTCCCCTGTGGCGAGCCTTAATAGATTAGGGACTAGGTCAAAGGAATGAGAGTGAGGAATTTGTGTTAGATGACCAAATCTTGCCTAAAATCGCAGTGTCTGCTGGGCAAATTCAAGACTTAATGACTAAATAAAAAACGAATAAAAAACTTAATGACAATTCTTGACTTCTTCTCTGCAGGCAAGCTGAATCTGGTAGACCTGGCTGGTTCTGAGAGGGTGTGG[A/T]AGTCTGGAGCAGAGGGGGAGAGACTGAAGGAAGCCCAGAATATTAATCGCTCACTGCTGGCTCTAGGTGATGTGATCCAGGCCCTGAAGGCCCACCAGACTCACATACCATTCAGGAACTCACGACTCACCTACCTGCTACAGGACTCGCTGGGAAAAGGCAACAAAACTGCCATGGTTGTTCAGGTAACAAAGATTTACCAAGACTTAGCTAACACTGTTGTGCTAACCCCATTTCATAATGACACATGTGAAATGCTGCCCATGGTTTGAGCCAAGGTACATTTGATCAGAATATACTCACAGTAAAGCCCATTGCACACTGAATCCAAAATCTTTGCATGTTAAAAAATAATGTCAACCTTGATCACATTTACACACTGCTTTCAAAATCTGATTGAGTTAGATTTCTTTGTTTTGTTAAAATTTTCACGTGCAAAAAAATGCATTTTGAGGGGTGTTTTGACAGTTTACAGCCACCATACAACCAAATCCCAAAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36081

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000059841	Nonsense	468	558	12	13

Genomic Location (Zv9):

Chromosome 16 (position 18609055)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	16651632
GRCz11	16	16559609

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAGACCTGGCTGGTTCTGAGAGGGTGTGGAAGTCTGGAGCAGAGGGGGAG[A/T]GACTGAAGGAAGCCCAGAATATTAATCGCTCACTGCTGGCTCTAGGTGAT

Long Flanking Sequence:

ACTGGGCCAAGTGTCATTACTGTTCTCATGTTTGCGTAGGTTTCTTTCGGGTGCTCTAGTTTCCCTCAAAGCCCAAAGACATGCAGTATGGGTGAACTGGATAAACTAAATTGACCCTATTGTATAAGTGTGTGATTGAGAGTGTGTGGGTAATTCCCAGCACTGAAGTTCACAAGTTAAGATACTCTCAGTGCTGGGTTGCGGCTGGAAGGGTGTTTATTGTGTGGAACATATGCCAAATAGTTGGTGGTTGATTCCCCTGTGGCGAGCCTTAATAGATTAGGGACTAGGTCAAAGGAATGAGAGTGAGGAATTTGTGTTAGATGACCAAATCTTGCCTAAAATCGCAGTGTCTGCTGGGCAAATTCAAGACTTAATGACTAAATAAAAAACGAATAAAAAACTTAATGACAATTCTTGACTTCTTCTCTGCAGGCAAGCTGAATCTGGTAGACCTGGCTGGTTCTGAGAGGGTGTGGAAGTCTGGAGCAGAGGGGGAG[A/T]GACTGAAGGAAGCCCAGAATATTAATCGCTCACTGCTGGCTCTAGGTGATGTGATCCAGGCCCTGAAGGCCCACCAGACTCACATACCATTCAGGAACTCACGACTCACCTACCTGCTACAGGACTCGCTGGGAAAAGGCAACAAAACTGCCATGGTTGTTCAGGTAACAAAGATTTACCAAGACTTAGCTAACACTGTTGTGCTAACCCCATTTCATAATGACACATGTGAAATGCTGCCCATGGTTTGAGCCAAGGTACATTTGATCAGAATATACTCACAGTAAAGCCCATTGCACACTGAATCCAAAATCTTTGCATGTTAAAAAATAATGTCAACCTTGATCACATTTACACACTGCTTTCAAAATCTGATTGAGTTAGATTTCTTTGTTTTGTTAAAATTTTCACGTGCAAAAAAATGCATTTTGAGGGGTGTTTTGACAGTTTACAGCCACCATACAACCAAATCCCAAAAAATCTAATTCTGTCACCTGGAG

Associated Phenotype:

Not determined