ZMP

ck2b

Ensembl ID:

ENSDARG00000077776

ZFIN ID:

ZDB-GENE-990415-29

Description:

Casein kinase II subunit beta [Source:UniProtKB/Swiss-Prot;Acc:Q91398]

Human Orthologue:

CSNK2B

Human Description:

casein kinase 2, beta polypeptide [Source:HGNC Symbol;Acc:2460]

Mouse Orthologue:

Csnk2b

Mouse Description:

casein kinase 2, beta polypeptide Gene [Source:MGI Symbol;Acc:MGI:88548]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23533	Essential Splice Site	Available for shipment	Available now
sa5924	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23533

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109258	Essential Splice Site	None	215	None	7

The following transcripts of ENSDARG00000077776 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 19 (position 27221967)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27152079
GRCz11	19	26736302

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTTGTGTCGCTGCGGCTAACATCGACCCCGGGAGATCCTTGAGGTAACG[T/C]CAGTAAACGCTTTTATCGCTATTATGAGCAGGGATGTGAAGTAATTTCGA

Long Flanking Sequence:

AATTAAGCTAAAATTGGCCTTTAATGTACAAGTGTAAATGAGTGTGCATGGATGTTTCCCAGAGTTGGGTAGCAGTTGGAAGGGCATCTGCTGCGTAAAACATATGCTGGATAAGTTGGCGGTTCATTTCGCTGTGGCAAGCCTTGATTAATAAAGGGACTAAAGTTAAGCCAAAAAGACAAATGAATGAATGAATAAAAGTGACATGCCCGCCAGCTACGGATCACGTGTCAGTTACTTTCATTGAAATATCAGTTTTTCTGACCTAAGTAATTGATCGCATCAATAGAATATTACACGAAAACGAATGCAAGGAAACCAAAAAGTGAATATAGAAAAGGAACGACTCTACAACTCAGAAACTACAACTCCTACAAGATCAGCGACGTGAGCGGAAGTGAGGTGACTTGTGATCACGTGATGCACAGCGGAAGCCTCCAATCAGCGTACAGTTGTGTCGCTGCGGCTAACATCGACCCCGGGAGATCCTTGAGGTAACG[T/C]CAGTAAACGCTTTTATCGCTATTATGAGCAGGGATGTGAAGTAATTTCGACGTTATGTTAATTAGCATCTATTTATTTTAATTCGCAGTTTATTTCACACATCACGACGCTCCCCGTTTTACATAATTGTGGATCAGTCGGCGAATTTGATGCGGCCTAGTTTGAAGCAGCGGCAAGCTAACCACACCTAGCATTAGCTGAGCACACAAACCAGAAAATCAACACTTATTAAAACTCTTGCCTGGCTGTTAAACATCACAATGTTTTTTCGGCCTTAGATGGAACTATTGTGCATATGTATTTTACTGTATTCGTCATGAGGCTTAAAATGTGACCAGCAGGCTATGCTAGCGTGCGTCAGACCAGTCCAGTCAATTGTTTACGTGAAAACTGTTTAGACTCGATGCAGTTTGTTATAAACATGTACTCATCTTAAACGTATTAGCAACGCAATATAATTTGCTACCCGAGACTTATTAACAGGGCAGTATTAACCTATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa5924

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109258	Essential Splice Site	123	215	None	7

The following transcripts of ENSDARG00000077776 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 19 (position 27217296)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	27147408
GRCz11	19	26731631

KASP Assay ID:

554-3778.1 (used for ordering genotyping assays)

KASP Sequence:

TTCACATGAGCTCCACTGAAACTTGAAGGAATGAATCTTTTGCCCTCTCC[A/T]GGCCTCTCTGACATTCCCGGCGAGGCTATGGTGAAGCTCTACTGCCCCAA

Long Flanking Sequence:

AATAAATGTTTTTTTATTTTTAATTTCACCATGTCTTCACTTTAGCATTTAAGCACAAATATAATGTAACTTGTACACTGTATTTCACAGCGCCTACTTTGCTGATTTATTTCATGAGCACAACCGTTACTGCATGTTAAAAGCCAAAAGGCGGATTAAAACACAAGGAGTAAATGTGGAAGACTTGTGATCTGACGAAAGAGTGTAAACAGTGGAGCCTGTAGCATTAGCTGGCCAGCCAGTTCAGTTTGTTTGGTTTGACCCAATCTTGGGTTTTAGGTAACATGAAGTCAGCTCAATTTTAGTCCCTCTTTGTTCTCATGGTACTATGGAGCATATAAGCTAAGCTACGTTCATGCTACCTAAAACCCAGAATTGGTGCAAACTTAACTGGCTAGCCAGCTAATCTGGCGTTATGGTACAGGCCGCTGGTCTTCAGGCAGTCCATTGTTCACATGAGCTCCACTGAAACTTGAAGGAATGAATCTTTTGCCCTCTCC[A/T]GGCCTCTCTGACATTCCCGGCGAGGCTATGGTGAAGCTCTACTGCCCCAAGTGTATGGATGTGTACACGCCGAAGTCATCCAGGCACCATCACACTGACGGAGCTTACTTTGGCACCGGCTTCCCTCACATGCTCTTTATGGTGCATCCCGAGTACCGGCCAAAAAGGCCTGCCAACCAGTTTGTGCCCAGGTTTGTCCTTCCTCCTGATTTTCTCAGATGAAGTCTACAGTTGTTCAGTTTGATCATAGTTGTTGTCTTTGTCCTCTTTCAGGCTTTATGGTTTTAAGATTCACCCAATGGCTTACCAGCTCCAGCTGCAGGCAGCCTCCAGCTTCAAGAGTCCCGTCAAAGCCATCCGCTAAACACCTGGGATGGGATGGGATGGGGTGGGGTGGGATGTCGGGTGGGTTGTGTGTCCGTCAACAAGGGCTCACTCTTCTCCTTCGATTTGACCGAGACTAACATTTAAATGTGGAGAGAGTGAGACTGTAAAACACT

Associated Phenotype:

Not determined