ZMP

camk2a

Ensembl ID:

ENSDARG00000053617

ZFIN ID:

ZDB-GENE-051113-72

Description:

calcium/calmodulin-dependent protein kinase type II subunit alpha [Source:RefSeq peptide;Acc:NP_001

Human Orthologue:

CAMK2A

Human Description:

calcium/calmodulin-dependent protein kinase II alpha [Source:HGNC Symbol;Acc:1460]

Mouse Orthologue:

Camk2a

Mouse Description:

calcium/calmodulin-dependent protein kinase II alpha Gene [Source:MGI Symbol;Acc:MGI:88256]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10214	Essential Splice Site	Available for shipment	Available now
sa43723	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10214

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
Order Allele From EZRC

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039571	Essential Splice Site	210	555	6	18
ENSDART00000039571	Essential Splice Site	210	555	6	18

Genomic Location (Zv9):

Chromosome 21 (position 42477940)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	43931591
GRCz11	21	43926757

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGGCWGTACTTCATTGCCATCAGATGGGTGTTGTKCACAGAGACTTAAAG[G/T]TAATTCAGCACTANNNNNNNNNNNAAATATGTCTTTAAGCATGTTTTTAGAGCACAATTGT

Long Flanking Sequence:

AATTAAATAATTCATCTATTTTTATTTTTATCATTATCACTATTATTATTATTAGTAGTATTAATTAATCTATTTTATTATTATTATTATTATTTATTTTATCTATTTATTTAATTGTTATTATTATTACTATTATTATTATTAATCTATTTCTTTTATTATTATTATTATTAATATTATTATTATTATTATTGATTATTTTAATTGTATTATTATTATATAGCAGATTTTGCATAAAACAAATGTTGCACATCTAGCCAAACTGCTATGTTTCATTTTTATATCCATATTTCTACAGTAAACAAAAAATAATAATAATTTGACAGGTTTAAATGCACATCTGTTGTGTGTTATTCATGTAAAGTGCAGCAAGTATATTATAACGAATTTAGTTTTTCTTTTTGTCTGTTTCCTTTCCCCCCTAAAGTCACTGCATTCAGCAGATTTTGGAGGCTGTACTTCATTGCCATCAGATGGGTGTTGTGCACAGAGACTTAAAG[G/T]TAATTCAGCACTAAAATATGTCTTTAAGCATGTTTTTAGAGCACAATTGTGATTAAATGATAAAATACAACACCAGTATTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACAACTAAGAGCAACAATGAATAAGTGCTGTAGGCAAGTTTCAGGTCTGTAAAGTCTAAGAAGGAAAGTATTAGTAATTTTTTAGTAATTTAGTAATTTTTATTATTAATTTTATAATTAATTAGTATTAAATATATCATTAAATATTATTGATTTCACAAAATAAATATACATTTATTAAAGAGTAAATATGCATAAAGCATGCACATCTATTTACATGCTTTTTAAGGGGGCGTTTATAAAGAGAATTCAGCAGGTCTCGACACCGAGCCTTGGAGAACTCTTCAAGCTTTGTAAGATACTTGGCCACTGAACCAGGGAAGTTTATATTGAGTTTATATAAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43723

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039571	Essential Splice Site	210	555	6	18
ENSDART00000039571	Essential Splice Site	210	555	6	18

Genomic Location (Zv9):

Chromosome 21 (position 42477940)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	43931591
GRCz11	21	43926757

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGCTGTACTTCATTGCCATCAGATGGGTGTTGTGCACAGAGACTTAAAG[G/A]TAATTCAGCACTAAAATATGTCTTTAAGCATGTTTTTAGAGCACAATTGT

Long Flanking Sequence:

AATTAAATAATTCATCTATTTTTATTTTTATCATTATCACTATTATTATTATTAGTAGTATTAATTAATCTATTTTATTATTATTATTATTATTTATTTTATCTATTTATTTAATTGTTATTATTATTACTATTATTATTATTAATCTATTTCTTTTATTATTATTATTATTAATATTATTATTATTATTATTGATTATTTTAATTGTATTATTATTATATAGCAGATTTTGCATAAAACAAATGTTGCACATCTAGCCAAACTGCTATGTTTCATTTTTATATCCATATTTCTACAGTAAACAAAAAATAATAATAATTTGACAGGTTTAAATGCACATCTGTTGTGTGTTATTCATGTAAAGTGCAGCAAGTATATTATAACGAATTTAGTTTTTCTTTTTGTCTGTTTCCTTTCCCCCCTAAAGTCACTGCATTCAGCAGATTTTGGAGGCTGTACTTCATTGCCATCAGATGGGTGTTGTGCACAGAGACTTAAAG[G/A]TAATTCAGCACTAAAATATGTCTTTAAGCATGTTTTTAGAGCACAATTGTGATTAAATGATAAAATACAACACCAGTATTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACAACTAAGAGCAACAATGAATAAGTGCTGTAGGCAAGTTTCAGGTCTGTAAAGTCTAAGAAGGAAAGTATTAGTAATTTTTTAGTAATTTAGTAATTTTTATTATTAATTTTATAATTAATTAGTATTAAATATATCATTAAATATTATTGATTTCACAAAATAAATATACATTTATTAAAGAGTAAATATGCATAAAGCATGCACATCTATTTACATGCTTTTTAAGGGGGCGTTTATAAAGAGAATTCAGCAGGTCTCGACACCGAGCCTTGGAGAACTCTTCAAGCTTTGTAAGATACTTGGCCACTGAACCAGGGAAGTTTATATTGAGTTTATATAAAG

Associated Phenotype:

Not determined