ZMP

cdk2

Ensembl ID:

ENSDARG00000026577

ZFIN ID:

ZDB-GENE-040426-2741

Description:

cell division protein kinase 2 [Source:RefSeq peptide;Acc:NP_998571]

Human Orthologue:

CDK2

Human Description:

cyclin-dependent kinase 2 [Source:HGNC Symbol;Acc:1771]

Mouse Orthologue:

Cdk2

Mouse Description:

cyclin-dependent kinase 2 Gene [Source:MGI Symbol;Acc:MGI:104772]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14988	Essential Splice Site	Available for shipment	Available now
sa41762	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14988

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000036581	Essential Splice Site	65	298	2	7

Genomic Location (Zv9):

Chromosome 11 (position 3286149)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	3237637
GRCz11	11	3305797

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTCGTGAGATCTCTCTGCTAAAAGAGCTCAATCACCCTAACATAGTCAAG[T/A]ATGTGCACTGTTTATGAATTTAGTCTCAAAACCAGTGAATATTTCAATGC

Long Flanking Sequence:

ACGACTAACTTTAGACATCAATATCAGTAATGAGTGTCAATTTCTGGAAATTGAGATTTATACATCATCTAAAAAAACCGAGTAATTAAGCTTTCCATTGATGGTTTGTTATGATACACTGAAAAAAACTATTTAAGTGGATTTACAAAAAACGTATGTTAAGTGGTTGCAATCAATTTATATGTTTTATATAATTTTTAAATATAAATTTAAACACACATATTAAGTAATATTCAACTTAATTTGTTTGTTTAAATTATCTTGTACAGTGCTCAGCATATACTGTATAAGTACACCCCTTACAAATGTGCCTTTAAGGCCAATAGGTCTCTGTTGTTTTCATATGCTGTAACATGAGCTGCTCCGTATAAACAAAAGTTTGTCCTAAATTCTGGATTGACATGATTTTGTTTGTTTTCAGGGAAACTGAAGGTGTTCCCAGCACTGCCATTCGTGAGATCTCTCTGCTAAAAGAGCTCAATCACCCTAACATAGTCAAG[T/A]ATGTGCACTGTTTATGAATTTAGTCTCAAAACCAGTGAATATTTCAATGCACAAATGTCCTCCTGGTTTGTGAGTTTTACAGTTTTCTTGCCTCCAGGTTGCGTGATGTGATACACACTGAAAATAAACTTTACTTGGTGTTTGAGTTTCTTCACCAAGACCTGAAGAGGTTTATGGACTCGACGTCTGTCAGTGGCATATCCTTGCCACTCGTGAAGGTGAGTTTAAGGTTTGAGCATTAGAAGAAGTGTTAACATCAGCTAAAGCTGCTGAACTGTTCCTTTAAAAATATATTATACTCAATATTACATAAATATATTTCTCCACATCATCACTTACTAACTTTTATTATCTCATACCAGATAGCTTTCAGTTCTTTTATAACCAGGATTTGCTTTGTGTGTTGGAGTACTTACATTTCTATGTTAAAATAGTTGTCTGTCCAGTATGAAAAAGAAATAAAAATATGTTAAACTGGTGCTAGTCTCAGATCAGCTCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41762

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000036581	Nonsense	217	298	6	7

Genomic Location (Zv9):

Chromosome 11 (position 3284159)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	3235647
GRCz11	11	3303807

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGGCACTGTTTCCTGGAGACTCTGAAATAGATCAGCTCTTCCGGATATTT[C/T]GAACTCTGGGCACTCCTGATGAGTCTATATGGCCTGGAGTTACATCAATG

Long Flanking Sequence:

AATGCATTCTTCAGAGTTTTGTTTAAACTAAGCATTCATTTCCTTTATTAATAGTATATATTATCTTTATATCTACTATTCATTTTCAGGTAGTGCTTGCAAGTGTCATATTTTCCATCTCTAGTACTGAATCTATTGTTTTTCTATTCATCCAGTGTTAGCATATATAGATTTATTTATTTATATTTGGTACGGATGACTTACACACTCTCAAAGTTGCATGATCTAATCTTAACTTGATCTTTCTCTATAGGTTGTAACTTTGTGGTACAGAGCTCCAGAGATTCTCCTGGGATGTAAATATTATTCTACAGCTGTTGACATCTGGAGTTTGGGCTGCATCTTTGCTGAAATGGTATTTTTTTTGTACTTTTTATCTAGCTTGTTGATAACTTAAGACATTCGTGTGCATTAGACTCCTCGTTTGCTTTTTATATCAGATTACTCGGAGGGCACTGTTTCCTGGAGACTCTGAAATAGATCAGCTCTTCCGGATATTT[C/T]GAACTCTGGGCACTCCTGATGAGTCTATATGGCCTGGAGTTACATCAATGCCAGACTACAAACCCTCCTTTCCCAAATGGGCTCGACAGGACCTGTCTAAAGTGGTGCCCCCCCTTGATGAAGATGGCAGAGACCTTCTCGGGGTAAGAGAGCAACAAAGATTATTTACTAAAATGGGGCGCTCACACTGGATGCGCCTTGCGCAAGTAAATCGCGATATTTGTACGTAATTAGATGCTTAAACAGTTTGAGTTTACTCAATCATTCGTGCAGTTTGCTTCATTCACTTCACAACAGACGCAAAATCACTCCAGTTTCCTTGCAAAATGCCTGACATGGATTTTGTTGAGAGGGTAGTTGTGCTTTATGTGCTATGAAAGGACTCGCTCAACGCCATTTCTGGGTCCATTAGATCCTTTAGAGGCGCACCCAGCTTGTTGAGTTTCAACTTATTTATTATTTAGCACATTTAACTGCAAGTTGAATTGCCCAAAGTGCTT

Associated Phenotype:

Not determined